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EBS Department at OGI
20000 NW Walker Rd
Beaverton, OR 97006
Phone: (503) 748-1070
Fax: (503) 748-1464

info@ebs.ogi.edu

EBS
Undergraduate Research Opportunities

General Information

Faculty in the Department of Environmental and Biomolecular Systems at the OGI School of Science & Engineering are committed to stimulating students' research interests at all academic levels. We seek motivated upper-level undergraduate students who are interested in hands-on research in preparation for graduate school in a related field of science or engineering. Students will have opportunities to interact with faculty, post-doctoral, doctoral and masters students while learning new skills and contributing to scientific research.

The availability of research opportunities differs with each faculty mentor. Some opportunities may be available only in the summer, while others will be able to accommodate students throughout the academic year. To apply for any of the research positions listed below, please contact the faculty mentor directly.

The OGI School of Science & Engineering is one of the four schools of Oregon Health & Science University, an equal opportunity, affirmative action institution. We particularly welcome applications from women, minorities, and individuals with disabilities.

 


Mentors and Projects


Area Project Mentor
Physical Oceanography Characterization of environmental stressors Antonio Baptista
Metallobiochemistry Metal ion homeostasis in an estuarine environment Ninian Blackburn
Metallobiochemistry Characterization of detoxifying cytochrome P450s P. Moënne-Loccoz
Microbiology Life without oxygen Michiko Nakano
Microbiology Control of gene expression in a saprophytic fungus Matt Sachs
Microbiology Distribution of archaea across the oxic/anoxic interface of Columbia River estuarine sediments Holly Simon
Contaminant Fate Environmental Degradation of Organic Pollutants Paul Tratnyek
Computational Toxicology Computational Modeling of Biological Systems Karen Watanabe
Metallobiochemistry Microbial manganese metabolism Jim Whittaker
Microbiology Bacterial oxidative stress response Peter Zuber

 


Project Descriptions


Project Title: Characterization of Environmental Stressors
Antonio Baptista (baptista@ebs.ogi.edu)

This project focuses on the characterization of environmental stressors in complex natural systems. We selected the Columbia River estuary where research is being actively used to address controversial management and sustainability issues (Bottom et al. 2001; USACE 2001) with the support of an advanced coastal observatory (Baptista 2002; Baptista 2004). Specific focus will be in characterizing the spatial and temporal variability of salinity, temperature and oxygen concentrations. The student will be introduced to state-of-the-art understanding of the estuary and its climate context, will be trained in the use of CORIE modeling tools (Baptista et al. 2004; Zhang et al. 2004 (Accepted)) and field instruments and procedures, and will design and conduct two model-assisted estuarine cruises to map the physical dynamics of specific estuarine environments: in principle, an estuarine turbidity maxima and a tidal flat. Physical data collected in the cruises will be integrated with multi-year databases of observations and simulations of water levels, velocities, salinity and temperature to provide specific physical context, in time and space, to biological and chemical samples simultaneously collected by other students during the cruises. [back]


Project Title: Metal ion homeostasis in an estuarine environment
Ninian Blackburn (ninian@ebs.ogi.edu)

Metal ions such as Fe, Cu, Zn, Mn, and Mo are essential to life. In general they form the active centers of a wide variety of enzymes with activities ranging from electron transfer to biosynthesis and biodegradation. However, these metals are also extremely toxic at higher concentrations, and cells have evolved complex mechanisms that ensure that metal ion concentrations are maintained at safe levels within the cell, without compromising the ability to selectively metallate important enzymes and pathways. These systems involve a critical balance between import, internal transport and export functions, and utilize novel transporters and chaperone proteins that maintain homeostasis. In addition to handling essential metal ion nutrients, cells must also be able to sequester and detoxify metal ion contaminants such as Cd, Hg, As, and Se. In this project we will investigate metal ion distributions across the Columbia River estuary (Blasco et al. 1999; Mierzykowski and Carr 2000). Of particular interest will be the levels of the essential metals Fe, Cu and Zn, and whether these nutrients are limiting. We will also investigate levels of the heavy metal contaminants Cd, As, Se, and Tl. To assess the effects of these contaminants on estuarine populations we will analyze the hemolymph of crayfish for the presence of these metals. This has a number of advantages: (a) protein components can be separated by chromatography and correlated with metal ion concentration (b) the proteins present in these fractions can be analyzed by mass spectrometry and their identity (metallothioneins, chaperones, transporters) determined by comparison with known or consensus sequences (c) crayfish from coastal rivers such as the Nehalem can be used as controls (d) exposure of the crayfish to elevated levels of metal ions under laboratory conditions can be used to calibrate dose-response data. The project will give undergraduate students training in techniques of metal analysis by ICP optical emission spectrometry, chromatographic separation and characterization of proteins by mass spectrometry, and other state-of-the-art methods. [back]


Project Title: Characterization of detoxifying cytochrome P450s
Pierre Moënne-Loccoz (ploccoz@ebs.ogi.edu)

Iron porphyrins (hemes) are utilized as enzyme cofactors throughout biology to activate molecular oxygen and catalyzed reactions such as monooxygenases essential to life. For example, cytochromes P450 (CYPs) enzymes are involved in the biosynthesis of a wide variety of lipophilic endogenous compounds such as steroids and prostaglandin, and they participate in the detoxication response to exposure to xenobiotic chemicals (e.g., drugs and environmental contaminants). Their catalytic function can metabolize these exogenous molecules, produce carcinogenic molecules, and as a by-product of these processes produce reactive oxygen species detrimental to the cell. While the number of CYP families and subfamilies identified via basic molecular techniques continues to expand, characterization at the molecular level of specific P450 enzymes remains very limited. Focused structural information can be obtained from the rich spectroscopic signatures of heme cofactors. Electronic absorption, Fourier-transform IR absorption, electron spin resonance, and resonance Raman spectroscopies are tools we will employ to study hemoproteins (Koo et al. 2000; Auclair et al. 2001; de Vries et al. 2003). The student will be exposed to protein purification, spectroscopic data acquisition, data handling, and data analysis. The student will also learn basic techniques relating to the control of the samples’ anaerobicity, oxygenation, and redox cycles. [back]


Project Title: Life without Oxygen
Michiko Nakano (mnakano@ebs.ogi.edu)

Oxygen is essential for human life and we cannot survive more than a few minutes in the absence of oxygen. However, some bacteria only survive in the absence of oxygen and others can grow either with or without oxygen. Our laboratory is investigating how a soil bacterium Bacillus subtilis can survive and grow when oxygen becomes limited. Elaborate regulatory pathways control gene expression in response to oxygen limitation. We utilize approaches of molecular genetics, reverse genetics, and biochemistry to study the mechanism of the oxygen-dependent global gene regulation. [back]


Project Title: Control of gene expression in a saprophytic fungus
Matthew Sachs (msachs@ebs.ogi.edu)

[Summer Student]

An undergraduate in the Sachs lab will involve molecular genetic analyses of gene expression in the model saprophytic fungus Neurospora crassa. N. crassa is different from the model yeast Saccharomyces cerevisiae and is a filamentous fungus that inhabits soil and aquatic environments. N. crassa more closely resembles higher eukaryotes than yeasts in features such as how gene expression is controlled by DNA methylation or by the circadian clock. Dr. Sachs was a co-PI on the NSF-sponsored project to sequence the N. crassa genome (Galagan et al. 2003). Because of this organism’s known genome sequence and its rich history as the subject for genetic, biochemical and cellular studies, the NIH subsequently funded a program project grant to systematically analyze the phenotypes of gene knockout strains; Dr. Sachs is a co-PI on this project. The student's work will focus on using selected knockout strains (a collection of which will be available prior to the onset of the work) to evaluate the consequences of specific mutations on the control of gene expression. Gene expression studies will involve analyses of the knockout's effects on post-transcriptional control (Fang et al. 2004) of gene expression or on the expression of genes located near the N. crassa telomeres. The choice of knockout strains to be used for the research project, and which area(s) will be examined, will be determined by assisting the REU students in formulating testable hypotheses as to why these strains would be predicted to have consequences in one or the other of these areas. For example, strains deficient in nonsense mediated mRNA decay because of a knockout of a gene essential for NMD would be hypothesized to be affected in both areas, because that is what is observed in yeast. These two areas are currently subjects of investigation in Dr. Sachs’ laboratory. Because the student may not have extensive experience with microbiological procedures, in addition to analyses at the molecular level (e.g., immunoblotting) in the Sachs lab, training in classical procedures (e.g., setting up and scoring genetic crosses, measuring growth rates) will be integral components of their research experience. [back]


Project Title: Distribution of archaea across the oxic/anoxic interface of Columbia River estuarine sediments Holly Simon (simonh@ebs.ogi.edu)

Microorganisms can, in theory, be useful as indicators of ecosystem health due to their rapid response times to changes in the environment. The low-temperature crenarchaeota represent a ubiquitous, and often abundant, but because of their recalcitrance toward growth in culture, largely unknown group of microorganisms (in terms of their physiology and ecological functions,). Diverse members of this group are known to be present in estuarine sediments, but nothing is known about their niches there (Abreu et al. 2001). The student working on this project will apply cultivation-independent methods (Simon et al. 2000), such as DNA extraction, Polymerase Chain Reaction-Single-Strand Conformation Polymorphism (PCR-SSCP) and real-time PCR to determine the population structure and abundance of members of the low-temperature crenarchaeota in Columbia River estuarine sediments with relation to oxygen availability at the sediment-water surface and in sub-surface layers. These data will be analyzed by the student to determine whether oxygen concentrations are a determining factor in the distribution of crenarchaeota in estuarine sediment layers. This project will expose the student to state-of-the-art cultivation-independent techniques used in environmental microbiology (Delong and Pace 2001), and results from the project will contribute to our understanding of estuarine microbial communities. [back]


Project Title: Environmental Degradation of Organic Pollutants
Paul Tratnyek (tratnyek@ebs.ogi.edu)

[Summer Student]

One important area of environmental science is the chemistry of organic pollutant degradation. Organic pollutants that are studied in the Tratnyek lab include pesticides, chlorinated solvents, explosives, and phenols. In all cases, the research will be concerned primarily with the kinetics and mechanisms of oxidation-reduction reactions that can degrade these compounds. This research helps to provide the basis for explaining and predicting the fate of organic pollutants in the environment. The understanding such research provides can lead to improved technologies for controlling pollutant contamination and can make regulatory decision-making a more scientific process. For the most part, the work involves experimentation in the laboratory at OGI, although some field sampling is possible. Analysis of pollutant concentrations will be done by gas chromatography and/or liquid chromatography with computer data acquisition. Details on Dr. Tratnyek's research can be found at http://www.ebs.ogi.edu/tratnyek/. [back]


Project Title: Computational Modeling of Biological Systems
Karen Watanabe (watanabe@ebs.ogi.edu)

Dr. Watanabe's research focuses on the development of computational models to investigate the biological fate of chemical xenobiotics, and the risks of exposure to such chemicals in different species. Computational models of living systems are used to simulate the processes underlying observed phenomena; predict outcomes that cannot be measured directly; analyze unexpected phenomena; and assess potential responses to stimuli. Research opportunities exist for an undergraduate to assist with the development of a physiologically based model of endocrine disruption in fathead minnows incorporating multiple levels of biological scale from gene expression to reproductive effects and chemical bioaccumulation in aquatic organisms (e.g., fish and crayfish). The broader impacts of these methods include: 1) providing a new perspective in how scientists view the biological processes involved in chemical xenobiotic bioaccumulation; 2) improving upon current methods (e.g., bioconcentration factors, biota-sediment accumulation factors based upon equilibrium partitioning theory) for analyzing data; and 3) develop more realistic approaches for predicting biota exposure to contaminants. Details on Dr. Watanabe's research can be found at http://www.ebs.ogi.edu/watanabe/. [back]


Project Title: Microbial manganese metabolism
James Whittaker (jim@ebs.ogi.edu)

Manganese, the fifth most abundant element in the earth’s crust, is an essential trace element required for all living systems. The availability of manganese in the environment depends on reactions that transform the soluble, reduced Mn(II) ion into the relatively insoluble higher manganese oxides. One of the most important biogeochemical transformations of manganese is performed by manganese-oxidizing bacteria (Stein et al. 2001) ubiquitous microorganisms that utilize the reducing power of Mn(II) ions in solution to drive cellular respiration, generating insoluble manganese oxides in the process. Biomineralization of the MnO x products leads to formation of manganese nodules in the environment. We will investigate the biochemistry of bacterial Mn(II) oxidation that underlies this important environmental element cycle. Manganese-oxidizing bacteria will be isolated from natural sources (including estuarial water samples) by enrichment culture. Colonies of Mn(II)-oxidizing bacteria will be identified by the formation of a yellow halo of Mn oxides on selective media, and the isolates will be further characterized by microscopic examination and by ribotyping PCR analysis of genomic DNA prepared from pure cultures. The physiology of Mn(II)-oxidation will be quantitatively investigated by measuring growth curves and determining the metabolic mass balance of metal metabolism. The molecular basis of biological metal oxidation will be investigated by electrophoretic resolution of membrane proteins (Brouwers et al. 1999) using activity staining to identify the Mn(II)-oxidization component (Francis et al. 2001). [back]


Project Title: Bacterial oxidative stress response
Peter Zuber (pzuber@ebs.ogi.edu)

Bacteria inhabiting an anoxic environment encounter reactive oxygen species (ROS) when shifted to an aerated environment rich in oxygen. ROS are also formed by UV-dependent photodynamic production from solar radiation. In response to accumulating ROS, processes are activated in bacteria that detoxify oxidants and protect the cell from their damaging effects. Control of such processes is carried out by global regulatory proteins that govern gene expression over a genome-wide scale (Zheng and Storz 2000). The student will examine the requirement of one such global regulator, Spx (Zuber 2004), in the response of a terrestrial bacterium to various treatments that result in oxidative stress. These treatments include anoxic to oxic shift in growth conditions as well as exposure to peroxides and ROS-generating agents. The student will examine the oxidative stress response phenotype of an spx mutant and the expression of genes controlled by Spx using reporter gene fusions. Together with the student we will determine if the spx gene is present in environmental samples collected from Columbia River estuary sediment and suspended-particle biofilms. Expression of spx in these samples will be tested using western-blot analysis and real-time polymerase chain reaction (RT-PCR). [back]


Links to Other Position Announcement Pages