Student Abstracts: Biology

A Biochemical and Computational Confirmation of ncRNAs in Ecoli. REBECCA ROHA (Gettysburg College, Gettyburg, PA, 17325) STEPHEN R. HOLBROOK (Lawrence Berkeley National Laboratory, Berkley, CA, 94720)

Non-coding RNAs (ncRNAs) are transcripts that do not code for a protein, but rather functional RNA molecules in that have roles in protein manufacturing, DNA replication, cellular control and many other processes. However important, ncRNAs are difficult to study because their sequences lack clear start and stop signals, making them practically invisible on the genome scale. Bioinformatics techniques must be designed for the classification and discovery of ncRNAs. The Positive Sample only Learning Algorithm (PSoL) suggested a highly accurate machine learning algorithm to identify ncRNAs by using a support vector machine to combine many ncRNA detection signals in order to distinguish ncRNA sequences from intergenic sequences. This method identified to predict 420 ncRNA sequences in the E. coli genome. The PSoL predicted sequences were then clustered using LocARNA, folded using RNAalifold, and interpreted. Several trials were completed to test LocARNA’s ability to cluster large amounts of sequences, correctly cluster identical sequences and to determine the effect of inaccurate sequences on the accurate clusters. Clusters were identified and a representative ncRNA from each was selected. For each chosen ncRNA, a Northern Analysis was completed; total E.coli RNA was extracted, the RNA was electrophoresed and transferred to a positively charged membrane, the membrane was then probed with non-isotopically labeled DNA complementary to the predicted ncRNA, hybridized, detected and developed. LocARNA successfully grouped the sequences into 9 clusters. ncRNA expression verification by Northern analysis is ongoing yet advancements have been made; DNA oligomers were successfully labeled and control RNA sequences were detected. A potential ncRNA has been identified, while further validation is necessary, a predicted sequence appears to be expressed. This work demonstrated that LocARNA is adequate clustering software for grouping predicted sequences into families. These findings are significant because they contribute to the search for a technique to identify and classify ncRNAs. Future research includes identifying more predicted ncRNAs as well as assigning the identified LocARNA clusters to known ncRNA families.

A Cell-Free Membrane Protein Factory Fueled by Rhodobacter Extracts. MICHAEL BELLISARIO (University of Illinois at Urbana-Champaign, Champaign, IL, 61820) PHIL LAIBLE (Argonne National Laboratory, Argonne, IL, 60439)

Membrane proteins play critical roles in many biological processes such as energy supply, solute import and export, and signal transduction. They are also ultra-critical to human health, comprising 60-80% of current drug targets. However, producing usable quantities of these proteins for structural and functional studies is quite challenging. Here, the goal is to eliminate this difficulty by creating a cell-free protein synthesis system specially designed for membrane proteins. This coupled transcription-translation system uses extracts (the source of all the enzymes and factors necessary for transcription and translation) derived from Rhodobacter sphaeroides cells, and membrane vesicles are introduced to the reaction in order to accommodate the membrane proteins being synthesized. This in vitro method has the capability to produce milligrams of target protein in a single milliliter reaction. In comparison, previously studied in vivo systems only produce milligrams of protein per liter of culture. The ultimate goal is to engineer this system so that it can be used generically and economically to produce target molecules for drug discovery.

A Computational Model for Analyzing the Biochemical Pathways of Matrix Metalloproteinase (MMP) 2&9 in Collagen Type IV Proteolysis. ELIZABETH O'QUINN O'QUINN (Wofford College, Spartanburg, SC, 29369) KARA KRUSE (Oak Ridge National Laboratory, Oak Ridge, TN, 37831)

Cardiovascular disease is the leading cause of death in first world countries. The imbalance of matrix degrading enzymes and structural proteins within the extracellular matrix of an arterial wall is a critical factor in cardiovascular disease processes. Matrix metalloproteinase-2 (MMP-2) and matrix metalloproteinase-9 (MMP-9) degradation of collagen type IV results in migration and proliferation of vascular smooth muscle cells; this can lead to further narrowing of a diseased artery. Kinetic modeling of proteolysis is an approach which can be used to understand complex systems by describing the enzyme’s mechanism and behavior quantitatively. In this research project, a computational model of biochemical pathways involved in activation and inhibition of MMP-2 and MMP-9 proteolysis of collagen type IV is being developed. Separate MMP-2 and MMP-9 models have been implemented within JSim, a software application developed by the University of Washington. Since MMP-2 and MMP-9 pathways overlap, the individual models will be integrated in the future. This MMP-2 model was also implemented in JDesigner, a tool of the Systems Biology Workbench, and DEVS, a discrete event system specification, for comparison of model environments. Various experimental methods for obtaining quantitative reaction rate parameters were explored, including high pressure liquid chromatography (HPLC) and florescence polarization. By pairing HPLC separation, largely by hydrophobic property, with spectrometry techniques, protein and peptide identification and quantification is possible. Previous literature suggests the use of HPLC to measure enzymatic activity, by using traces of the product/substrate itself as an internal standard. An experimental protocol for the measurement of the enzymatic activity of MMP-2 and MMP-9 is being developed. HPLC baseline standards for the individual substrates and enzymes are currently being measured and optimized. After baseline standards are determined the MMP enzymatic activity can be determined. The HPLC experimental results will be analyzed to derive the reaction rate parameters needed by the computational model. The use of HPLC methods to analyze the enzymatic activity of MMP-2 with collagen type IV and other correlated substrates provides parameters which cannot be obtained through literature. This research is in collaboration with the Vascular Research Laboratory at the University of Tennessee Medical Center in Knoxville.

A High Throughput Method of Screening Mutant Arabidopsis Plants for Improved Biofuel Capacity Using Infrared Microspectroscopy. SIMONE PARK (State University of New York at Stony Brook, Stony Brook, NY, 11794) LISA MILLER (Brookhaven National Laboratory, Upton, NY, 11973)

Acyl-esterification is one of the most common modifications that occurs within the plant cell wall, and contributes to the covalent cross-linked polymerizations found there. These cross-linkages are found between lignocelluloses, components found in the cell wall, and contribute to the recalcitrance and complexity of the overall plant and prevent effective degradation for conversion into bioethanol. In this study, stems from 12 mutant Arabidopsis thaliana plants representing 6 distinct mutant lines were analyzed with Fourier Transform Infrared (FTIR) microspectroscopy to develop a high-throughput method of screening and characterizing Arabidopsis lines. Cell wall components were extracted with ethanol in 2 ways and point spectra were taken to determine the extent of the 1740 cm-1 peak corresponding to the vibrational carbonyl group characteristic of esters. Results from cluster analysis and acyl content from the microspectroscopy revealed that samples presented variabilities inherent to the complexity of the cell wall structure and to those attributed with sample preparation. Imaging of cross-sectioned stems was also performed, and it was found that the acyl content in the section was radially heterogeneous. More careful sample preparation for microspectroscopy and use of synchrotron light for imaging to gain greater spatial resolution in the cell wall will be valuable in improving this high throughput screening method.

A Rational Approach for Crystallization of Proteins in Deuterated Media. ALEXIS RAE DEL CASTILLO (California State University, Chanel Islands, Camarillo, CA, 93012) HUGH O'NEILL (Oak Ridge National Laboratory, Oak Ridge, TN, 37831)

Neutron crystallography is emerging as a powerful tool for the study of protein structure and dynamics. In neutron crystallography the neutrons interact weakly with the nucleus of an atom and therefore are a highly penetrating and non-destructive probe. Unlike x-rays, which interact with the electron cloud surrounding an atom, neutrons can detect lighter atoms such as hydrogen in the presence of heavier ones and differentiate between them. The aim of this study was to determine how deuterium oxide influences the crystallization behavior of proteins compared to crystallization in hydrogenated media. This will allow a rational design approach for growing protein crystals for neutron crystallography. In order to achieve this goal a range of proteins were selected for crystallization studies. Some proteins, such as aprotinin, cytochrome c, B-lactoglobulin and papain were obtained commercially. In addition, two variants of GFP, from Aequorea victoria and A. coerulescens, were over-expressed in Escherichia coli in hydrogenated and deuterated media. The recombinant proteins were then purified to homogeneity by three-phase partitioning and anion exchange chromatography. The conditions for crystallization of each protein were determined using a high throughput platform that can screen 1536 different crystallization solutions simultaneously. Each protein produced crystals in several different solutions. The conditions that produced crystals were then subjected to a second screening procedure called Drop Volume Ratio Temperature (DVR/T) to further optimize and refine the chemical and physical parameters that produced crystals in the initial screen. A DVR/T phase diagram has been completed for aprotinin, cytochrome c, B-lactoglobulin A and papain in hydrogenated buffer. Currently, a DVR/T screen in deuterated buffer is underway for these proteins.

Neutron crystallography is emerging as a powerful tool for the study of protein structure and dynamics. In neutron crystallography the neutrons interact weakly with the nucleus of an atom and therefore are a highly penetrating and non-destructive probe. Unlike x-rays, which interact with the electron cloud surrounding an atom, neutrons can detect lighter atoms such as hydrogen in the presence of heavier ones and differentiate between them. The aim of this study was to determine how deuterium oxide influences the crystallization behavior of proteins compared to crystallization in hydrogenated media. This will allow a rational design approach for growing protein crystals for neutron crystallography. In order to achieve this goal a range of proteins were selected for crystallization studies. Some proteins, such as aprotinin, cytochrome c, myoglobin, phospholipase and others were obtained commercially in their purified form. Green fluorescent protein (GFP) and rubredoxin, were over-expressed in Escherichia coli and purified from cell-free extracts. The optimal conditions for crystallization were determined using a high throughput platform that can screen 1536 different crystallization conditions simultaneously. Expression of recombinant proteins was induced with isopropyl ß-D-1-thiogalactopyranoside (IPTG). The cells were lysed by sonication followed by centrifugation. The proteins were purified by ion exchange chromatography and size exclusion chromatography. The purification process was monitored by UV/visible absorption spectrophotometry, circular dichroism spectroscopy, fluorescence excitation/emission and sodium dodecyl sulfate (SDS) polyacrylamide gel electrophoresis (PAGE). Currently the 1536 screen in H₂O media has been completed for several of the proteins mentioned above and the experiments to determine how D₂O influences crystallization conditions are underway. In addition, techniques to produce per-deuterated forms of GFP and rubredoxin are being developed by adapting E. coli to grow in D₂O based media.

Accuracy of sequence-based identifications of filamentous fungal species using ITS2 and LSU rDNA sequences. IVY MCDANIEL (Scripps College, Claremont, CA, 91711) TAMAS TOROK (Lawrence Berkeley National Laboratory, Berkley, CA, 94720)

As fungi are becoming increasingly relevant to human society, the number of scientists qualified to identify fungal species using traditional methods is dwindling. There is therefore a need to develop tools that use standard molecular methods to accurately identify filamentous fungi at the species level. Our laboratory examined the effectiveness of making DNA sequence-based identifications of a collection of filamentous fungi by comparing the sequences of different variable regions of the ribosomal DNA to those in the NCBI Genbank database. By examining a conserved gene such as the ribosomal DNA, we hypothesized that there would be low variability among the sequence of conspecific organisms, but enough variability in the sequence of different species to clearly separate the organisms. We analyzed sequences from the D1/D2 domains of the large-subunit rDNA of 159 organisms from 85 species and 44 genera, and the ITS2 sequences of 28 organisms from 23 species and 13 genera. In both regions, the sequences by themselves did not appear to be variable across all genera and divisions of fungi to the point that the sequences could be used as an accurate identifier of a single species.

Agt1 Promoter Sequence Analysis in the Collaborative Cross Parental Mouse Strains. JEANNA KIDWELL (Christopher Newport University, Newport News, VA, 23606) BRYNN VOY (Oak Ridge National Laboratory, Oak Ridge, TN, 37831)

The Collaborative Cross (CC) is a unique mouse genetic reference population being generated at the Oak Ridge National Laboratory. This cross will consist of approximately one thousand recombinant inbred (RI) strains of mice derived from eight parental strains that were chosen for their genetic and phenotypic diversity. Each strain will contain a unique combination of alleles from the eight parental genomes, creating a population with genetic and phenotypic diversity on par with the human population and a novel resource for the study of heritable disease in humans. We are using the CC population to study the association between adipose tissue production of Angiotensinogen (Agt) on obesity and type 2 diabetes. Agt is the substrate for Angiotensin II, a bioactive hormone that regulates insulin sensitivity as well as many other physiological processes. We sequenced the Agt1 promoter region (about 1.2 kilobases upstream from Agt1) in the 8 CC parental strains in an attempt to identify regulatory polymorphisms that cause wide variation, up to 100-fold, of adipose Agt mRNA expression levels across the CC parental strains. DNA was extracted from mouse ear clips using a modified "Hot Shot" protocol (alkaline lysis followed by neutralization). The Agt promoter was amplified using Polymerase Chain Reaction with a series of six oligonucleotide primers. DNA sequencing was performed at the UTK Molecular Biology Resource Facility. Sequence analysis indicates several single nucleotide polymorphisms between the strains as well as a three base pair deletion present in three strains (A/J, NZO, and CAST) and not present in the other five strains (C57BL/6J, 129, NOD, PWK, WSB). Future experiments will be directed towards determining the impact of these polymorphisms on Agt transcription.

Amplification of Methylated DNA Sequences that Retains mCG Epigenetic Marks. DANNY KOHUT (New York University, New York, NY, 10003) JOHN J. DUNN (Brookhaven National Laboratory, Upton, NY, 11973)

It has been shown that tumor cells contain an extensive amount of methylated DNA, which could be used in finding cancer before the onset of symptoms or to monitor reoccurrence. By amplifying DNA in such a way that retains methylation patterns, a small amount of DNA can be used to detect cancer. The pGEM5 vector was methylated using HpaII Methyltransferase, an enzyme that recognizes CCGG sequences and adds a methyl group to the 2nd cytosine residue. The DNA was then cut with HpaII and MspI to check for complete methylation; the latter enzyme is able to cut methylated CmCGG sequence while the former cannot. An attempt was then made to amplify the methylated pGEM5 sequence using F29 amplification with dnmt1 Methyltransferase, but without success. Our second and novel method required HeLa DNA, which comes from a cancerous cell line, to be cut with MseI, gel purified and then joined to a synthetic DNA cassette. The purified ligation mixture was then bisulfite modified, which transforms all non-methylated cytosine residues into uracils. PCR amplification of the top strand with bisulfite-modified specific primers produced a large amount of DNA where the only remaining CG’s are those that were originally methylated. M.SseI Methyltransferase will then add a methyl group to these sites to re-form mCG’s, which are then affinity purified using the methyl-binding proteins MBD2b and MBD3L1 and then either hybridized to a microarray or sequenced.

Analyzing the Structure and Function of Novel Cytochromes from a Natural Microbial Community. ANNA SIEBERS (University of California, San Diego, La Jolla, CA, 92093) MICHAEL P. THELEN (Lawrence Livermore National Laboratory, Livermore, CA, 94550)

The Richmond mine in Iron Mountain, California, provides an unusual ecosystem suitable for the growth of microbial biofilms which produce many unique proteins. Through iron oxidation, these proteins facilitate acid mine drainage (AMD). Because this habitat is extremely acidic, survival is an extraordinary feat and the process of environmental selection is rare. In order to understand the mechanisms by which these organisms oxidize iron and gain electrons for energy, biochemical studies were applied. More specifically, column chromatography, spectrophotometry, and gel electrophoresis were used to determine the proteins present in different biofilms. Two specific locations of the mine researched were the AB drift and Ultraback C (UBC), which were both found to contain at least five different types of protein and a large amount of heme-bound cytochromes. Another application of these methods was to investigate proteins playing a major role within the community; one protein selected was cytochrome 579 (Cyt₅₇₉) due to its abundance in the biofilm, iron oxidizing potential, and signature absorbance of 579nm. The structure and function of Cyt₅₇₉ could be characterized by the isolation of its heme, which was completed using column chromatography; however, one of the challenges has been liberating the heme from the column. Further research, including acid-base and temperature profiling of Cyt₅₇₉ should help elucidate its structural changes within alternate environments and metabolism within the community.

Angiotensinogen Expression in Collaborative Cross Offspring. ADAM LUNDQUIST (Christopher Newport University, Newport News, Va, 23606) BRYNN H. VOY (Oak Ridge National Laboratory, Oak Ridge, TN, 37831)

The Collaborative Cross (CC) is an emerging population of recombinant inbred (RI) lines of mice designed to untangle complex webs of genetic interactions. The CC, now being implemented at Oak Ridge National Lab (ORNL), is being created from 8 diverse inbred strains of mice bred to produce 1000 RI strains, with every resulting strain containing a portion of the genome from each of the 8 parental strains. The genetic and phenotypic diversity of these 1000 RI strains will model that found in human populations, making the CC a valuable resource for dissecting the genetic contributors to complex traits such as obesity and hypertension[1]. This diversity, coupled with the known genotypes of the animals, will be utilized to map and dissect the genetics of complex traits, which are phenotypes produced from the interaction of multiple genes. We are interested in obesity a complex trait involving many genes interacting within multiple metabolic pathways. One such gene known to play a role in both obesity and hypertension is angiotensinogen, Agt. Agt is a vascular constrictor expressed in adipose tissue; its expression varies widely among the eight CC parental strains. In order to study Agt expression in the intermediate CC generations, those whose genomes have yet to be fixed by inbreeding (strict brother-sister mating for 20 generations), we extracted RNA from adipose tissue, reverse transcribed it into complementary DNA (cDNA), and utilized quantitative Polymerase Chain Reaction (qPCR) techniques to determine mRNA expression levels. Agt expression levels ranged widely (~ 15-fold) across the sampling of CC mice, indicating tha the diversity of this molecular trait in CC mice reflects that of a human population. Our results provide insight into the effects that mixing diverse genetic backgrounds have on Agt expression in these RI mice and will lead to future mapping of genomic loci involved in complex metabolic traits.

Aquatic Macroinvertebrates of Wetland R at Argonne National Laboratory, Illinois: A Comparative Study of Pond Populations and Water Health. LEAH JOHNSTON (University of Illinois at Urbana-Champaign, Champaign, IL, 61820) KIRK LAGORY (Argonne National Laboratory, Argonne, IL, 60439)

Wetlands are essential for sustaining dynamic and healthy environments. The presence of wetlands has decreased during the past one hundred years due to human-caused disturbances. In order to comply with wetland protection laws, Wetland R was created to replace the 1.8 acres of natural wetlands that were destroyed during the construction of the Advanced Photon Source at Argonne National Laboratory in DuPage County, IL. Construction of Wetland R began in August 1990. The purpose of this study was to survey and compare the aquatic macroinvertebrate populations in Wetland R to those in upper Freund Pond. Upper Freund Pond is located northwest of building 617 at Argonne National Laboratory. Aquatic macroinvertebrates are used as bioindicators of water quality. Based on the populations found in both locations, the qualitative health of each was determined and compared. Samples were taken from each site using a dipnet and were sorted with a series of sieves to find specimens. Once collected, specimens were examined and identified to the genus level. The known sensitivity towards pollution levels of each genus was determined from the literature to determine the water health of each area. The water surface area was measured weekly at Wetland R. A total of 15 genera were discovered. There was a higher genus diversity present in Wetland R (10 genera) than in Freund Pond (seven genera). Of the genera discovered at each site, eight of the 10 (80%) in Wetland R and three of the seven (43%) at Freund pond were sensitive or moderately sensitive towards water pollution. Biomonitoring (the utilization of biological responses to assess environmental changes) using the sensitivity levels of the collected genera from each location indicated that the water quality at Wetland R exceeded that of Freund Pond. It is recommended that annual monitoring of aquatic macroinvertebrates in Wetland R continue. The utilization of laboratory-based chemical analysis on the water of Wetland R is recommended to provide additional information on water quality. Maintaining good water quality in Wetland R will promote high species diversity.

Bystander Analyses of X-ray Microbeam Induced gamma-H2AX Punctate Signals in the Human Mammary Epithelial Cell Line 184V. MICHELLE SALCEDO (Diablo Valley College, Pleasant Hill, CA, 94523) ELEANOR BLAKELY (Lawrence Berkeley National Laboratory, Berkley, CA, 94720)

Damage to DNA can be caused by direct and indirect effects of ionizing radiation absorbed by irradiated cells. Radiation damage to DNA can trigger a sequential cascade of responding DNA-repair molecules that can be visualized microscopically with the use of specific fluorescently-labelled antibodies and immunohistochemistry. The focus of my research has been to use a 12.5 keV X-ray microbeam produced at the LBNL Advanced Light Source beamline 10.3.1 to target a dose stripe of 100 microns wide on a population of 184V Human Mammary Epithelial Cells (HMEC) and to process the cell samples for DNA damage response markers as a function of time and distance from the dose stripes. This allows me to study both targeted and untargeted cells. The response of untargeted cells not in the radiation field is called a “bystander effect”. Comparisons have been made after doses of either a relatively high dose stripe of 100 cGy or a relatively low dose stripe of 10 cGy. Gamma-H2AX and 53BP1 are the two DNA damage response markers I have studied. Some differences were noted in the phosphorylation response of each of these markers in the nuclei of irradiated HMEC. Gamma-H2AX and 53BP1 appear to co-localize, but with a different time course. I developed a scoring system to compare the morphological differences noted in these two DNA damage response markers in large montages of HMEC irradiated with the X-ray microbeam. Comparisons were made with unirradiated control cultures. The results indicated that a significant diversity of gamma-H2AX fluorescent signals exist in the unirradiated control possibly due to asynchronous cells varying in different stages of the cell cycle or culturing conditions. Irradiated areas expressing a high response of gamma-H2AX were an efficient indicator of the location and width of the stripe of dose, especially within the 100 cGy 10 minute montage image. Physical measurements of the stripe confirmed widths of 100 to 110 microns verifying the accuracy of the microbeam used. Histograms of different levels of intensities of gamma-H2AX expression were created using the data collected by using the devised scoring system. The data analyzed in the histograms demonstrated potentially novel fingerprints of the background fluorescent signal, the direct radiation damage effect, and the bystander effect. Future replication of this experiment is needed to validate significance of these results.

Carbon Sequestration in an Agricultural Ecosystem under Elevated Carbon Dioxide Levels. DANIEL OLSON (Iowa State University, Ames, IA, 50011) JULIE JASTROW (Argonne National Laboratory, Argonne, IL, 60439)

Atmospheric carbon dioxide has increased by 30 percent since the Industrial Revolution and is predicted to continue increasing at an accelerated rate. The increase in CO2 allows terrestrial plants to grow faster and thus increases carbon inputs to the soil. Higher levels of CO2 have shown increased carbon sequestration in deciduous forest and grassland soils, but the effect on agricultural soils requires further investigation. In 2001 a free air carbon dioxide enrichment (FACE) site was constructed in central Illinois to study the effects of elevated CO2 conditions on a corn-soybean crop rotation. FACE allows experimental areas to be exposed to elevated levels of CO2, while minimizing the change in sunlight, humidity, wind speed, and so forth. Soil from four FACE plots releasing CO2 with a concentration of 550 ppm CO2 and four rings exposed to ambient CO2 levels (approximately 370 ppm) were sampled prior to planting in 2001 and again in April 2006. In both ambient and elevated CO2 plots, soil carbon decreased between 2001 and 2006 based on whole soil carbon concentration; however, elevated CO2 plots did not lose as much soil carbon as did ambient CO2 plots. The loss of whole soil carbon over the study period is unexpected. It is most likely due to a difference in land use and management before 2001. The difference in carbon loss may be due to increased soil inputs in elevated CO2 plots. The amount of carbon sequestered in each of the soil fractions will show where carbon loss is occurring. The change in carbon concentration of each soil fraction between 2006 and 2001 must be found. That data will show where carbon is sequestered in this agricultural ecosystem.

Characterization of Actin as a Cofactor for the Adenovirus Proteinase. HAN ZHU (Massachusetts Institute of Technology, Cambridge, MA, 2139) WALTER F. MANGEL (Brookhaven National Laboratory, Upton, NY, 11973)

A good model system for the development of effective protease-inhibition based anti-viral agents (drugs) is human adenovirus (AVP), because AVP is essential for the production of infectious viruses. AVP is found to require viral cofactors, which regulate the activity of AVP in time and space, for maximal activity. Actin, one of the most abundant proteins in the cell and a major component of the cytoskeleton, is believed to be an AVP cofactor due to the high homology of its c-terminus with the 11 amino acid peptide viral cofactor pVIc. The binding of monomeric actin to AVP allows for its activation and the cleavage and degradation of the cytokeratin-18 network of a host cell, releasing newly formed virions. Using a spectrofluorometric assay with optimized buffer conditions to preserve the native structure and monomeric form of actin, insights can be gained by characterizing the binding interaction between actin and AVP. Although the reaction rates were lower than expected, assays varying the actin concentration with constant concentrations of AVP suggest tight binding between actin and AVP. The KM of the AVP-actin complex was measured to be 7 µM, very similar to the measured KM of the AVP-pVIc complex, suggesting that the binding of actin does not change substrate affinity. Rather, the binding of actin changes the properties of the enzyme itself, or the kcat (determined by VMAX). In addition, actin stimulates AVP in the presence of either one of the two viral cofactors (DNA and pVIc), allowing us to conclude that actin binds to two independent sites on AVP. Furthermore, through the use of competition assays with DNA, we were able to begin to estimate the binding affinity between actin and AVP with and without its viral cofactor pVIc. A better understanding of the interaction between actin and AVP should reveal new targets for anti-viral drug development.

Comparison of Land Management Practices on Common Wood Nymph Butterfly Populations. TARA SCHWASS (Western Illinois University, Macomb, IL, 61455) ROD WALTON (Fermi National Accelerator Laboratory, Batavia, IL, 60510)

Diversity of habitat and variety of wildlife has been increasing through restoration and land management techniques at Fermi National Accelerator Laboratory (Fermilab). These land management techniques are crucial to restoring and sustaining the natural habitats and native species of the area. This study examined the effects of land management techniques on the burned restored prairie, unburned restored prairie and mowed non-native grasslands and how these techniques affected local butterfly populations of Cercyonis pegala, the common wood nymph. Originally native to the prairie, the common wood nymph now occupies a wide range of habitat that includes not only prairie but also non-native grasslands, open woodlands, fields, marshes, savanna, and road sides. Transect counts were used to survey the abundance of wood nymphs for each of the five sites studied. A similar study performed last year included two of the same sites studied this year. Results were analyzed using a t-test, Mann-Whitney U-test, Spearman correlation, and Pearson correlation. Our results indicated the prairie had significantly more butterflies than the non-native grasslands and also weather variables did not significantly affect butterfly counts. Our results differed greatly from the study performed last year where non-native grasslands had more butterflies than the native prairie site. These varying results are likely due to the timing of the land management techniques at the sites. However, other possible explanations for the results may be vegetation differences in growth, abundance, and density, and/or butterfly behavior. A continuation of this study should include the same sites after a new season of burning and mowing to examine long-term effects of land management techniques and also to gain a better understanding of butterfly ecology at Fermilab.

Crystallization and Crystallography Analysis of Amidohydrolase Enzyme from the Structure Genomic Project. ARSHAD MEHMOOD (Medgar Evers College, Brooklyn, NY, 11226) D. KUMARAN (Brookhaven National Laboratory, Upton, NY, 11973)

The crystal structure of an amidohydrolase (target ID 9355e) has been obtained to 2.35 Å resolution. Diffraction data were collected at the National Synchrotron facility of Brookhaven National Laboratory (beam-line X29). The crystals obtained by the sitting drop vapor diffusion method were 0.1 x 0.06 x 0.05 mm3 in dimension. The crystals belong to the tetragonal space group P4 with unit-cell parameters a=b=144.74 Å, c =100.96 Å. In this tetragonal crystalline structure of 9355e there was one dimer per asymmetric unit. Amidohydrolase includes the families of enzymes that catalyze the cleavage of wide range of substrates bearing amide or ester functional groups at Carbon and Phosphorus centers. This enzymatic reaction is common in various metabolic processes thus it is important to understand this reaction at the molecular level. Therefore, by knowing the three-dimensional structures of these enzymes and their active sites, we can predict their function and the catalytic mechanism.

Crystallization and Preliminary X-ray Crystallographic Analysis of the Archaeal Tryptophan Regulator, TrpY. JACQUELYN CAFASSO (Cornell University, Ithaca, NY, 14853) MARK CHANCE AND BABU MANJASETTY (Brookhaven National Laboratory, Upton, NY, 11973)

The TrpY protein from the archaeon Methanothermobacter thermautotrophicus is a transcription regulator of the metabolically expensive tryptophan biosynthetic pathway. Although the trp genes in Bacteria, Archaea, and eukaryotes share a common ancestry, diverse mechanisms regulate their expression. The TrpR repressor in E. coli has been extensively studied, but the structure and mechanism for repression by the TrpY regulator from archaea remains unknown. Furthermore, TrpY shows very little sequence homology with the TrpR tryptophan regulator in E. coli, and although bioinformatics studies indicate that the fold is conserved among other archaeal transcription regulators, the sequence similarity to TrpY is nonetheless very low. Native crystals of TrpY were successfully grown in 0.1M sodium acetate and 1.6M ammonium sulfate at room temperature using the hanging-drop vapor diffusion method. Initial diffraction tests and the search for a suitable cryo-protectant were performed at beamline X3A of the National Synchrotron Light Source (NSLS). X-ray diffraction data was collected at beamline X29 of the NSLS to 2.9 Å resolution. Preliminary data analysis revealed that the crystals fall in the tetragonal space group with cell parameters a=b=87Å, c=147Å. Methods to solve the structure of TrpY using heavy atom derivatives are currently underway. Using crystallographic X-ray analysis to solve the structure is important to gain insight into the TrpY mechanism of repression as well as important features of transcription regulation and evolutionary history in the Archaea. This project is a small portion of a larger project under investigation in collaboration with the Department of Microbiology at The Ohio State University.

Crystallographic studies of two bacterial antibiotic resistance enzymes: Aminoglycoside Phosphotransferase (2’’)-Ic and GES-1 ß-lactamase. LAURA BYRNES (Rensselaer Polytechnic Institute, Troy, NY, 12180) CLYDE SMITH (Stanford Linear Accelerator Center, Stanford, CA, 94025)

Cytochemical Investigation of Lignin Redistribution During Thermochemical Pretreatment. BRITNEY PENNINGTON (Florida Institute of Technology, Melbourne, FL, 32901) TODD VINZANT (National Renewable Energy Laboratory, Golden, CO, 89401)

Due to the increasing demand for oil, the United States has developed starch ethanol programs, but corn cannot support both the food and fuel industries. Cellulosic ethanol is a promising alternative to starch-based ethanol but is more difficult to generate cost-effectively because biomass is inherently resistant to degradation. Lignin, the polyphenolic compound in plant cell walls, contributes to this recalcitrance by inhibiting hydrolytic cellulases and presents an obstacle to producing bioethanol. Dilute acid pretreatment of biomass removes only a fraction of the lignin content, and yet at high temperatures, sufficient enzymatic digestion can still occur. To address this paradox, this study utilized microscopy and cytochemical stains to determine temperature’s role in lignin redistribution during dilute acid pretreatment. All of the cytochemical stains used to detect lignin had evenly distributed staining patterns at 80ºC but became concentrated towards the cell edges as temperatures approached 160ºC. Temperature’s effect on the biomass surface was also investigated using scanning electron microscopy. Starting at 140ºC, half-sphere droplets appeared on the tissue surfaces and their morphologies seem to coalesce into larger spheres at higher temperatures. Round droplets were also observed using the light microscope. It has been hypothesized that the melted lignin is pushed out of the cell wall, possibly by increased hydrogen bonding between adjacent cellulose microfibrils, and forms spheres due to hydrophobic forces. Understanding lignin redistribution and its resulting implications on cell and tissue structure will help biologists explain the effects of pretreatment on biomass.

Effects of Burrow Characteristics on Temperature in Simulated Owl Burrows. LUCY TRAN (University of California, Los Angeles, Los Angeles, CA, 90024) COREY A. DUBERSTEIN (Pacific Northwest National Laboratory, Richland, WA, 99352)

Effects of Phosphate on the Bioreduction of Iron Oxyhydroxide. KATHRYN FENSKE (University of Illinois at Urbana-Champaign, Urbana, IL, 61801) EDWARD O'LOUGHLIN (Argonne National Laboratory, Argonne, IL, 60439)

Green rusts are mixed ferrous/ferric hydroxides minerals that form in suboxic environments as products of Fe(III) oxide reductions by dissimilatory iron-reducing bacteria (DIRB), and as such play an important role in Fe cycling in aquatic and terrestrial environments. DIRB can conserve energy and also support growth by coupling the oxidation of organic compounds to the reduction of Fe(III) to Fe(II) with the potential formation of Fe(II)-bearing minerals such as magnetite, siderite, and green rust. The overall processes of the formation of a specific Fe(II)-bearing mineral, such as green rust, are controlled by several factors including microbial physiology, solution chemistry, and FeIII mineralogy. This experiment examines the effects of phosphate on the type(s) of Fe(II)-bearing minerals resulting from the bioreduction of a Fe(III) oxyhydroxide (lepidocrocite). Experimental systems consisted of sealed serum vials containing lepidocrocite with formate provided as an electron donor. Different amounts of phosphate were added to each system and they were inoculated with Shewanella putrefaciens CN32, a model DIRB. Lepidocrocite reduction was monitored by measuring Fe(II) by the Ferrozine assay. Biomineralization products were identified by X-ray diffraction. Analyses of results indicate that green rust formed when phosphate was present at concentrations of 100µM or higher, while magnetite formed at phosphate concentrations below 100µM. Green rusts have recently been shown to be capable of reducing a number of organic and inorganic contaminants (including carbon tetrachloride and U(VI). Therefore, understanding how factors such as phosphate concentration can contribute to the formation of green rusts may assist in efforts to design remediation strategies for cleanup of subsurface contamination.

Elucidating a Practical Approach to the Study of Eukaryotic Genes: Expression of Eukaryotic Zebrafish Proteins in Prokaryotic E coli Expression Vectors. ASHLEY FRANK (Elmhurst College, Elmhurst, IL, 60126) FRANK COLLART (Argonne National Laboratory, Argonne, IL, 60439)

Production of heterologous protein via expression in prokaryotic expression vectors has been extensively employed in recent years to yield significant amounts of protein for downstream characterization and analysis. The use of such vectors offers a practical, economical route for the production of protein, eliminating cost and time inefficiencies accompanying protein isolation from the native protein-producing organism. While bacterial expression systems have been optimized for cloning prokaryotic genes, further investigation is needed to optimize these systems for production of more complex eukaryotic proteins. The cell machinery of a bacterial expression system is limited with respect to the production of eukaryotic proteins as these proteins are derived from more intricate, compartmentalized cells and often require specific enzymes for post-translational modifications and protein folding. Since many of the enzymes and machinery necessary for the successful expression of eukaryotic proteins are lacking in the current bacterial expression systems, study of such proteins has been avoided using these methods. To accommodate the requirements of eukaryotic protein production in bacterial expression systems, periplasmic expression vectors have been constructed and modified using previous cytoplasmic vector templates to optimize the expression and solubility of eukaryotic proteins. Such vectors direct proteins to the periplasm where bacterial chaperones reside to aid in proper protein folding and disulfide bond formation which is required by many eukaryotic proteins, thus increasing protein solubility and recovery potential. In a study to determine a successful approach to the production of eukaryotic proteins, 96 select Zebrafish genes were amplified, cloned into two different periplasmic vectors (pBH31 and pMCSG19p), induced to express the heterologous target protein, and screened for positive expression and solubility. Results suggest that pMCSG19p, which harbors a solubility fusion tag, was superior in performance, with respect to the production of soluble proteins for these 96 targets. In addition, expression in this vector resulted in a relative increase in solubility of targets containing predicted disulfide bonds and signal peptides, suggesting that pMCSG19p may provide an effective route for the production of complex eukaryotic proteins. The solubility results for proteins produced in pBH31, however, were comparable to the solubility results of these same 96 targets produced in the cytoplasmic vector, pMCSG7, suggesting that this vector not only does not improve solubility of eukaryotic proteins, but also may not shunt the proteins to the periplasm for proper expression. Further studies employing different vector solubility tags or manipulation of cytoplasmic physiology may be required for the optimization of eukaryotic protein expression in bacterial expression systems.

Engineering novel gene-regulatory RNA aptamers. YUVRAAJ KAPOOR and LESLEY LARA (University of California, Berkeley, Berkeley, CA, 94609) JAY KEASLING (Lawrence Berkeley National Laboratory, Berkley, CA, 94720)

Aptamers are RNA sequences that bind to target molecules and consequently regulate gene expression in a ligand-dependent fashion. They are frequently employed in nature to couple fluctuations in the concentration of a metabolite with changes in gene expression. Upon binding a small molecule, aptamers sequester the ribosome binding site [RBS] of a cis mRNA and repress translation. Synthetic aptamers eliminate the need to rely upon pre-existing biological molecules as the source of binding structure. Generation of synthetic aptamers occurs through in vitro selection, iterative rounds of enrichment and amplification which eventually select for an RNA molecule with high binding affinity [~100uM] and specificity. Through a combination of directed evolution and rational design we generated functional, ligand-binding RNA structures that control the cis-expression of mRNA transcripts in response to tetramethylrhodamine [TMR], a small fluorescent dye that is cell permeable. Iterative rounds of reselections and binding assays in in vivo like conditions have generated 3 isolates of TMR-binding aptamers. When incorporated into constructs with self-cleaving hammerhead ribozymes, such molecules will provide general tools for simultaneously varying the expression levels of toxic intermediates in engineered pathways such as that of the anti-malarial drug, Artemisinin.

Evaluation of Cloning Vectors pMCSG8 and pMCSG10 to Increase Protein Solubility. JESSICA BEARDEN (Universtiy of Texas-Pan American, Edinburg, TX, 78539) SHIU MOY (Argonne National Laboratory, Argonne, IL, 60439)

A major obstacle in the high-throughput production of purified proteins, as conducted in the Protein Structure Initiative, is to routinely obtain soluble proteins using the standard cloning vector pMCSG7. It is important that cloners release soluble proteins to the purification group because insoluble proteins cannot be purified. Evaluation of cloning vectors pMCSG8 and pMCSG10 was conducted to recover soluble proteins that failed to be soluble using pMCSG7. pMCSG7 has a histidine affinity tag at the N-terminus, followed by a tobacco etch virus(TEV) protease recognition site, followed by a ligation independent cloning site, followed by another histidine tag at the C-terminus. pMCSG8 is structurally similar to pMCSG7 with the exception of a binding loop(S-loop) of the chaperone protein GroES between the histadine tag and the TEV protease recognition site, while pMCSG10 has a Glutathione-S-Transferase(GST) in place of the S-loop. Selected samples were transformed and then cloned into the desired vector. Competent Escherichia coli cells were induced to uptake the recombinant DNA. Expression and solubility analysis was conducted using sodium dodecyl sulfate polyacrylamide gel electrophoresis. Clones that both expressed and were soluble were then frozen down and released to the protein purification team. pMCSG8 was able to recover ten percent of the samples tested. pMCSG10 analysis is still underway. pMCSG8 results implicate incorporation of a feedback loop in the high-throughput production of proteins at the Structural Biology Center at Argonne National Laboratory.

Expression and Purification of a Vaccinia Virus Nudix Family Decapping Enzyme. BRANDI WENGER (Diablo Valley College, Pleasant Hill, CA, 94523) STEPHEN R. HOLBROOK (Lawrence Berkeley National Laboratory, Berkley, CA, 94720)

The Nudix (nucleoside diphosphates linked to another moiety x) hydrolase superfamily of proteins is characterized by its conserved 23 amino acid signature sequence. The motif is found among eukaryotes, bacteria, archaea and viruses. Proteins of the Nudix hydrolase superfamily perform a wide variety of functions using diverse substrates. The Nudix proteins have very low sequence conservation outside the signature and have a large amount of structural variation around a conserved structural core. Protein D10 contains this motif and is conserved in all poxviruses. In recent research, it was revealed that without the Nudix motif expressed in protein D10 of the laboratory prototype of poxviruses, vaccinia virus (VACV), the virus was unable to successfully target a host. Altering the motif in protein D10 caused VACV to lose its ability for mRNA decapping. With this ability lost, VACV no longer had the ability to suppress synthesis of cellular proteins and regulate its own gene expression. Solving the structure of protein D10 would allow an inhibitor to be designed to prevent poxviruses from successfully targeting a host. VACV D10 was cloned and expressed in Escherichia coli bacterial cells as a maltose binding protein (MBP) fusion (pMalD10) and a His-tagged protein (pETD10). Although expression is low for both the fusion and tagged versions of protein D10, preliminary results indicate that purification by affinity chromatography is feasible. Further experiments are underway to improve expression and purification of protein D10 with the goal of obtaining sufficient homogeneous material to perform crystallization experiments.

Expression, Purification, and Small Angle X-Ray Scattering of DNA Replication and Repair Proteins from the Hyperthermophile Sulfolobus solfataricus. STEPHANIE PATTERSON (Del Mar College, Corpus Christi, TX, 78404) STEVEN M. YANNONE (Lawrence Berkeley National Laboratory, Berkley, CA, 94720)

Vital molecular processes such as DNA replication, transcription, translation, and maintenance occur through transient protein interactions. Elucidating the mechanisms by which these protein complexes and interactions function could lead to treatments for diseases related to DNA damage and cell division control. In the recent decades since its introduction as a third domain, Archaea have shown to be simpler models for complicated eukaryotic processes such as DNA replication, repair, transcription, and translation. Sulfolobus solfataricus (S. so) is one such model organism. A hyperthermophile with an optimal growth temperature of 80°C, S. so protein complexes and transient interactions should be more stable at moderate temperatures, providing a means to isolate and study their structure and function. Here we provide the initial steps towards characterizing DNA-related S. so proteins with small angle X-ray scattering (SAXS). We focused on three S. so proteins: Sso0257, a cell division control/ origin recognition complex homolog, Sso0768, the small subunit of the replication factor C, and Sso3167, a Mut-T like protein. E. coli cells transformed with the pet21a expression vector containing the S. so gene of interest were grown to logarithmic phase. Protein expression was induced with 1mM Isopropyl ß-D-1-thiogalactopyranoside (IPTG). Cells were harvested by centrifugation. Proteins were extracted by sonication, then the extracts heated to denature any contaminating E. coli proteins. Soluble protein was purified by Ni-affinity column chromatography in a Fast Protein Liquid Chromatography (FPLC) system. S. so proteins were eluted with an imidazole gradient and collected as fractions, then concentrated to a range of 1-10mg/ml. S. so proteins were analyzed with SAXS at multiple concentrations for both short and long exposure times. The Sso0257 sample was determined to be a 1:1 combination of monomer and dimer states. Sso0768 was found to be a complex mixture of multimeric states. Molecular envelope reconstruction from SAXS data for Sso3167 revealed a novel structural component which may function as a disordered to ordered region in the presence of its substrates and/or protein partners.

Extracellular Translocation of Recombinant MtrC and OmcA by Type II Secretion System. SHIRABRANDY GARZA (Washington State University, Pullman, Wa, 99163) LIANG SHI (Pacific Northwest National Laboratory, Richland, WA, 99352)

Marine Mussel Adhesive Protein Production in Saccharomyces cerevisiae. KINDRA ENGELS (Washington State University, Pullman, WA, 99163) FRANK ROBERTO (Idaho National Laboratory, Idaho Falls, ID, 83415)

The adhesion proteins used by Mytilus edulis (blue mussel) to cling to surfaces in an aqueous environment have many features, such as strength and water resistance, that make them a potentially useful adhesive. Three M. edulis foot proteins (Mefp) will be the focus of this study: Mefp-1 (115 kDa), which forms a hardened sheath around the byssal threads, Mefp-2 (42-47 kDa), which adds stability near the attachment site, and Mefp-3 (5-7 kDa), which may act as an adhesion primer. Because it takes 10,000 mussels to obtain 1g of an individual native mussel adhesive protein, a more practical production method was investigated. Mussel adhesive protein genes were introduced into clones of Saccharomyces cerevisiae, with Mefp-1 in clone #21, Mefp-2 in clone QTB10, and Mefp-3 in clone #11. S. cerevisiae cultures (20 liters) were grown in a 2% galactose SC-U induction medium at 30 °C with shaking and harvested by centrifugation. Growth was monitored by spectrophotometry. Cells were homogenized and lysed in an acidic breaking buffer with glass beads in a bead beater. After centrifuging again, the recombinant mussel adhesive protein in the supernatant was purified by dialysis with nanopure water and a sodium borate solution (pH 8.5). Centrifugal filter devices concentrated the proteins. Protein concentration was determined using a Bradford assay with bovine serum albumin as a standard. Samples were analyzed by electrophoresis. Results from growth curves revealed that 20 L cultures had optimal harvest times after 24 hours and cell pellet wet weights of 114.55g (#21), 102.69g (QTB10), and 185.512g (#11) were obtained. Electrophoresis of #21 and QTB10 purified proteins resulted in bands near the expected size ranges of recombinant proteins Mefp-1 and Mefp-2. In conclusion, the results suggest that adhesive protein production in S. cerevisiae cells is possible and that purification methods successfully concentrated the adhesive proteins. This method could potentially be used to produce recombinant adhesive protein quantities that would normally require the sacrifice of thousands of mussels. The M. edulis recombinant adhesive proteins obtained may be used for various studies involving the proteins’ adhesive potential and further formulation development.

Metal Repartition and Expressed Genes in Spinal cord of Rats. SERITTA HILL (Chicago State University, Chicago, IL, 60628) DR. CHRISTINE GERIN (Argonne National Laboratory, Argonne, IL, 60439)

Specific metals such as Fe, Cu, and Zn have been shown to accumulate in the central nervous system (CNS) in several neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS). Metal involvement has been linked to neural degeneration in late onset neurodegenerative diseases. The hypothesis is that similar cellular patterns of degeneration might occur in spinal cord injury. The first aim addresses the question of metal repartition in spinal cord of rats, using X-ray fluorescence. The second aim addresses the question of variation in expression targeted genes in spinal cord using quantitative real time polymerase chain reaction (QRT-PCR). Rats were anaesthetized with sodium pentobarbital (60mg/1000g) injected intraperitoneally. Spinal cord segments T9 and T13 were excised. RNA isolation was performed using TriZol protocol (Sigma). RNA was purified using RNA clean up kit (Qiagen). Two µl of the RNA sample were used to determine the optic density (OD) and the concentration in ng/µl. Three RNA dilutions were made to construct a concentration curve for c DNA and QRT-PCR. cDNA was synthesized using 10µl of RNA followed by QRT- PCR using 11 housekeeping genes (primers). Most of our RNA OD results were 2.0 for the 260/280 ratio and for the 260/230 they were in the ranges of 1.8-2.2. The concentration of RNA samples ranged from 5.4ng/µl to 1200ng/µl. OD curves illustrated that RNA absorbed the highest at 260 nm. RT-PCR demonstrated two curves for each RNA concentration and it illustrated that the c DNA with their various primers amplified properly. In conclusion the housekeeping genes were expressed in our samples. In the future the house keeping genes will be compared to our gene of interest. For example, BDNF. The Advance Photon Source (APS) beam line was used to train on cardiomyocytes in order to use it in the future to measure the sub cellular trace metals such as Zn, Fe, and Cu in our spinal cord samples. Experimental work was performed in collaboration with Argonne National Laboratory and Northwestern University.

Methodological analysis of an Amidohydrolase from Psychroflexus torquis and its crystal structure. JENNIFER LEVIA (Medgar Evers College, Brooklyn, NY, 11225) DR. BROWN / D. KUMARAN (Brookhaven National Laboratory, Upton, NY, 11973)

Amidohydrolases, superfamily of metallo-dependent hydrolases, a large group of proteins that show conservation in their 3-dimensional fold (TIM barrel). To gain structural insights into the substrate specificity and enzymatic mechanism, one of this family member 9355a was selected for structure determination as a structural genomics target. This study will be useful in understanding this enzyme family at molecular level and will provide structural basis for designing drugs for specific target. The target amidohydrolase enzyme was crystallized using sitting drop vapor diffusion technique at room temperature. Square shaped crystals of dimensions 0.2 x 0.2 x 0.1 mm3 were obtained in a day or two. X-ray diffraction intensities were collected at the X29 beamline of National Synchrotron Light Source (NSLS). Crystals diffract to at least 2.4 Å and belong to the tetragonal space group I41 with unit-cell parameters a=b=192.56 Å, c=277.0 Å. Assuming 12 molecules of 50,000 Da per asymmetric unit, the Matthews coefficient is 2.2 Å3 Da-1 corresponding to an estimated solvent content of 43% by volume of the unit cell. The structure determination process is in progress.

Modeling Estimated Personnel Needs for a Potential Foot and Mouth Disease Outbreak. KIRSTEN SIMMONS (North Carolina State University, Raleigh, NC, 27607) DR. PAM HULLINGER (Lawrence Livermore National Laboratory, Livermore, CA, 94550)

Foot and Mouth disease (FMD) is a highly contagious viral disease affecting livestock that was last detected in the US in 1929. The prevalence of FMD in other countries, as well as the current potential for this virus to be used as a form of agroterrorism has made preparations for a potential FMD outbreak a national priority. All 50 states were surveyed via e-mail, telephone and web search to obtain emergency response plans for FMD or for foreign animal diseases in general. Information from 35 states was obtained and analyzed for estimates of resources needed to respond to an outbreak. These estimates were expanded and enhanced to create a spreadsheet tool that could be used by individual states to better understand the personnel that would be needed to complete various tasks during an outbreak response. Personnel estimates were varied according to facility type and scaled by size. The estimates were then coupled to the output from FMD outbreaks simulated using the Multiscale Epidemiological/Economic Simulation and Analysis (MESA) model at Lawrence Livermore National Laboratory to assess the personnel resource demands on a response agency over the course of an outbreak response.

Non-Invasive Indexing of Red and Gray Fox Populations at Brookhaven National Laboratory. PATRICK MALLIN (College of William and Mary, Williamsburg, VA, 23186) JENNIFER HIGBIE (Brookhaven National Laboratory, Upton, NY, 11973)

The red fox (Vulpes vulpes) and the gray fox (Urocyon cinereoargenteus) have sympatrically inhabited the greater Long Island area over the last several hundred years. In recent years, speculation has grown regarding the population size of each species. While the red fox has historically been known to adapt well to ecological disturbances, including those of an anthropogenic nature, and is largely considered to have a thriving population in the Long Island area, recent studies of the last thirty years suggest the gray fox populations have struggled with such anthropogenic disturbances of the last century. A previous Brookhaven National Laboratory (BNL) study in 2006 confirmed the presence of gray Fox on BNL property using non-invasive fecal DNA analysis via mitochondria DNA markers and automated camera documentation. This project further studied the extent of the gray fox presence on BNL property for the 2007 season by using the non-invasive techniques of fecal DNA extraction and automated field cameras. Gray fox presence was confirmed through both methods over the course of the study. While apparently much less common than the red fox, the gray fox species appears to be present and established on the BNL site and, presumably, in similar habitats throughout the Long Island area.

Optimization of a Batchwise Immobilized Metal Affinity Chromatography Protocol. DAVID KONOPKA (Kalamazoo College, Kalamazoo, MI, 49006) FENG YANG (Pacific Northwest National Laboratory, Richland, WA, 99352)

Phosphate Enhanced Uranium Reduction. RACHEL FAIRBANK (Tompkins Cortland Community College, Dryden, NY, 13053) ANTHONY V. PALUMBO (Oak Ridge National Laboratory, Oak Ridge, TN, 37831)

A common contaminant found at DOE sites is uranium, which characteristically leaches into groundwater and surrounding soils. Remediation of these sites is therefore a DOE focus. Current technologies mainly consist of pump and treat technologies which have the disadvantage of being invasive and ineffective in areas with low flow velocity. Total cleanup costs using existing technologies are estimated to exceed a total of $220 billion, making it worthwhile to investigate alternative methods of uranium remediation. One focus for remediation is the stabilization of uranium through reduction of mobile U(VI) to its less soluble and immobile form U(IV). One possibility is by stimulating existing microbial communities to reduce uranium. Previous experiments had demonstrated the ability of electron donors’ ethanol and methanol to stimulate bioreduction of uranium. This experiment investigated the idea of phosphate being a limiting nutrient in bioreduction of uranium. Anaerobic microcosms were created using contaminated soil from the Oak Ridge Field Research Center. Samples were analyzed at specific time points throughout the experiment using a Kinetic Phosphorescence Analyzer which measured the amount of soluble uranium. This experiment found that the addition of phosphates led to immediate removal of uranium from solution. This effect was observed to be independent of the presence of an electron donor, as a similar effect was observed in the microcosms with only phosphates added. Therefore, these results imply that reduction is due to a chemical interaction with the phosphates rather than due to stimulation of the microbial community.

Protein Complex interaction assays of Shewanella oneidensis MR-1 proteins and its Relevance to Bioremediation Techniques. NATHAN ROBERTS (Marquette University, Milwaukee, WI, 53233) FRANK COLLART (Argonne National Laboratory, Argonne, IL, 60439)

Identification of interacting proteins is a first step toward understanding the biological function of a protein. Mapping the protein interactions throughout a genome can define the communication network. The network can be used to predict how the organism will respond to changes in the environment. The bacterium Shewanella oneidensis MR-1 was used as a model organism for identification of interacting proteins. This bacterium can survive in the presence of heavy metals and its metabolic machinery can render these metals insoluble. This characteristic opens up many possibilities for Shewanella oneidensis or its proteins to be used in bioremediation of areas afflicted with radioactive and/or heavy metal contamination. Since very little is known about specific interacting proteins in Shewanella oneidensis, interacting proteins in Escherichia coli have been identified which contain high sequence similarity to Shewanella oneidensis proteins. Proteins are generally considered to have a similar function when protein sequences are 50+ % identical. Open reading frames coding for proteins from Shewanella oneidensis were amplified from genomic DNA and cloned into E. coli expression vectors using molecular techniques. The proteins were screened for expression and solubility and the soluble proteins purified at a milligram scale. Each protein was expressed with an N-terminal his-tag to allow for interaction screening using a pull-down assay. This technique has allowed for mass scaling up and purification of chosen targets which then has allowed for identification of interacting proteins and further research into functionality.

Purification and Characterization of Recombinant Aequeorea coerulescens Green Fluorescent Protein from Escherichia coli. MATT PEOPLES (Earlham College, Richmond, IN, 47374) HUGH O'NEILL (Oak Ridge National Laboratory, Oak Ridge, TN, 37831)

Green Fluorescent Protein (GFP) is a single chain polypeptide that forms a fluorescent chromophore by rapid cyclization and subsequent oxidation of residues Ser₆₅-Tyr₆₆-Gly₆₇. It is widely used as a fluorescent tag for in vivo investigations. In this study an efficient procedure was developed for the isolation and characterization of enhanced recombinant Aequeorea coerulescens GFP (aceGFP) that was over-expressed in Escherichia coli JM109. The first step employed three-phase partitioning to precipitate GFP using ammonium sulfate and tert-butanol. This was followed by dialysis and anion exchange chromatography. The purification procedure was monitored by UV/Visible absorption spectrophotometry, circular dichroism spectroscopy, fluorescence excitation/emission, and sodium dodecyl sulfate (SDS) and native polyacrylamide gel electrophoresis (PAGE). Interestingly, two variants of GFP separated during anion exchange chromatography. The first variant (GFP₄₇₈) absorbed maximally at 478nm with a fluorescence emission maximum of 505nm. The yield was 3.04mg GFP₄₇₈/g cell paste. The second variant (GFP₄₉₃) had a maximum absorbance at 493nm and an emission maximum of 509nm. The yield of this protein was 11.4mg GFP₄₉₃/g cell paste. Comparison of the UV/Visible and circular dichroism absorption spectra of the two isoforms indicate that the environments of their chromophores are different. Denaturing SDS-PAGE demonstrated that the lengths of their polypeptide chains are identical; however GFP₄₉₃ migrated less than GFP₄₇₈ by native PAGE, indicating a difference in the tertiary/quaternary structural characteristics of the two isoforms. GFP has been successfully purified from recombinant E. coli in good yield, and the two resulting isoforms of aceGFP have been characterized. Small angle x-ray scattering will be used to further investigate the structural properties of these two proteins in solution.

Purification of Chromatin-binding Protein YieF for Cancer Prodrugs. LISA WANG (State University of New York at Stony Brook, Stony Brook, NY, 11794) YAN-BIAO ZHANG (Brookhaven National Laboratory, Upton, NY, 11973)

To further our understanding of the roles of YieF protein in chromate transformation and detoxification, the crystal structure of YieF protein can be observed and the binding site and activity site of the protein can be found. YieF is a bacterial enzyme from Escherichia Coli (E. Coli) with prodrug-reducing activity involved in cancer chemotherapy. Through its prodrug capabilities, the activity of YieF ultimately reduces the toxicity of chemotherapy on normal cells. YieF has chromate-reducing capabilities without redox recycling, and reduces the toxic contaminant Cr+6 to Cr+2 directly using four-electron transfer by transferring three electrons to chromate and one electron to oxygen. The plasmid pYBZ49, containing the YieF gene in a pTYB3 expression vector, was used to overproduce the YieF protein in the E. coli BL21(DE3) strain. Recombinant YieF was purified by using affinity chitin-binding column and size exclusion chromatography column. Crystal conditions were tested. From the crystals we routinely observed, the crystal conditions were defined and we were able to see crystals at 2 microns. Purified YieF protein was used to test different crystal formation conditions to ultimately solve the protein structure.

Relative Quantitation using Real-time Polymerase Chain Reaction Techniques (RT-PCR) to Compare Expression Levels of Genes Relevant to Pellet Formation in Aspergillus niger. TORRI RINKER (Oregon State University, Corvallis, OR, 97330) SCOTT BAKER (Pacific Northwest National Laboratory, Richland, WA, 99352)

Biology Abstracts: