Sabine Rech, Ph.D.
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
| University of Santa Clara | B.S. | 1984 | Biology |
| San Jose State University | M.A. | 1987 | Microbiology |
UC Davis | Ph.D. | 1992 | Microbiology |
| UCLA | Postdoc | 1998-1999 | Micro and Mol Gen |
| 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 D. 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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