Sabine Rech, Ph.D.
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Associate Professor
Department of Biological Sciences
San José State University
Department of Biological Sciences
One Washington Square
San José, CA 95192-0100
Duncan Hall, Room 336
Telephone:
(408) 924-4832
FAX: (408) 924-4840
E-mail: srech@email.sjsu.edu
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COURSES TAUGHT
Micro 101 - General Microbiology
Micro 122 - Bacterial Diversity
Micro 127 - Microbail Physiology
Biol 255M - Seminar in Advanced Biology - M & M
TRAINING
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University of Santa Clara |
B.S. |
1984 |
Biology |
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San Jose State University |
M.A. |
1987 |
Microbiology |
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UC Davis |
Ph.D. |
1992 |
Microbiology |
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UCLA |
Postdoc |
1998-1999 |
Micro and Mol Gen |
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Michigan State University / Center for Microb. Ecology |
Postdoc |
1998-1999 |
Env. Microbiol. |
POSITIONS
1996-1997 Lecturer , University of Southern California, Department
of Biological Sciences
1998-1999 Research Associate, Michigan State University, Center for
Microbial Ecology
1999-2005 Assistant Professor of Microbiology, San Jose State University,
CA
2005-  Associate Professor of Microbiology,
San Jose State University, CA
RESEARCH
My research interests lie in the area of environmental microbiology and microbial
diversity. Currently my laboratory is involved in two active research projects.
The first project focuses on the isolation of bromination enzymes from bacteria
in marine or high salt environments. We have isolated microorganisms capable of
brominating organics from a salt evaporation pond as well as the slime of a marine
invertebrate worm classified as an acorn worm. Our studies involve the identification of the bacteria by isolating and sequencing their 16SrRNA genes as well as the isolation
and characterization of the bromination enzymes, which include bromoperoxidases.
The second project focuses on the investigation of the microbial diversity in the
soil of salt marshes in the process of natural restoration as well as the role of
the denitrifying organisms in this process. We are using restriction fragment length
polymorphism (RFLP) to begin to understand the diversity throughout the growing
season. This technique involves the extraction of the total community DNA from the
soil followed by the amplification of the bacterial 16SrRNA genes. The amplified
genes are grouped into operational taxonomic units (OTUs) by restriction digests
and representatives are sequenced. We are examining three marshes, which are in various restoration stages ranging from a mud flat to an almost completely restored
wetland. Both projects require the isolation and quantification of DNA and protein
using a highly sensitive method. This research will be greatly supported by the grant of fluorometer from Turner BioSystems.
PUBLICATIONS
1. Komives, C., S. Rech and M. Mc. Neil. 2004. Laboratory Experiment on Gene
Subcloning For Chemical Engineering Students. Chemical Engineering Education
38: 212-215
2. Boothby, J. T., R. Miller, S. Rech and R. Hicks. 2004
Teaching Phagocytosis
using Flow Cytometry. Microbiological Education 5:36-41
3. McNicholas PM, M. Mazzotta, S. A. Rech and R. P. Gunsalus. 1998. Functional
dissection of the molybdate-responsive transcription regulator, ModE, from Escherichia
coli. J. Bacteriol. 180:4638-4643.
4. Hu, Yonglin, S. Rech, R.P. Gunsalus and CO C. Rees. 1997. Crystal Structure
of ModA, a molybdate transport protein, complexed with molybdate and tungstate.
Nature Structural Biology 4:703-707.
5. Schroeder, Imke, S. Rech, T. Krafft and J. Macy. 1997. Purification and
characterization of the selenate reductase from Thauera selenatis. J. Biol.
Chem. 272:23765-23768.
6. Mc Nicholas, Paul M., S. Rech and R. Gunsalus. 1997. Characterization
of the ModE DNA binding sites in the control regions of modABCD and moaABCDE
of Escherichia coli. J. Mol. Micro. 23:515-524.
7. Rech, Sabine, C. Wolin and R. Gunsalus. 1996. Properties of the Periplasmic
ModA Molybdate-Binding Protein of Escherichia coli. J. Biol. Chem. 271:2557-2562.
8. Rech, Sabine, U. Deppenmeier and R. Gunsalus. 1995. Regulation of the
Molybdate Transport Operon, modABCD, of Escherichia coli in Response
to Molybdate Availability. J. Bacteriol. 177:1023-1029.
9. Rech, Sabine and J. Macy. 1992. The Terminal Reductases for Selenate and
Nitrate Respiration in Thauera selenatis are two Distinct Enzymes. J. Bacteriol.
174:7316-7320.
10. Macy, J. M., S. Rech, G. Auling, M. Dorsch, E. Stackebrandt and L. I.
Sly. 1993. Thauera selenatis gen. nov., sp. nov., a Member of the Beta Subclass
of Proteobacteria with a Novel type of Anaerobic Respiration. Int. J. Sys. Bacteriol.
43:135-142.
C. Research Support
Ongoing Research Support
Co-Prinicpal Investigator on Research Experience for Undergraduates Grant, NSF (Title:
Research by Undergraduates using
Molecular Biology Applications (RUMBA)). 5/2004-5/2007.
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