The purple membrane of Halobacterium halobium is a photon activated photosynthetic membrane composed of lipids and a well characterized protein (bacterio-opsin) complexed with the chromophore retinal. The structure and membrane physiology of the purple membrane has received considerable attention in the past ten years. Genetic analyses of this membrane have only been underway for the past two years. The gene for bacterio-opsin (bop) has been cloned and numerous spontaneous mutants have been characterized. It is clear that the synthesis of purple membrane is regulated by environmental factors such as light and oxygen tension but the genetic basis for regulation has been difficult to track. Our discovery of a gene (brp) associated with the expression of the bop gene has provided the first insight into a possible regulatory mechanism. We propose to investigate the role of the brp gene relative to the synthesis of purple membrane under a variety of culture conditions which suppress or enhance purple membrane synthesis. We also propose to develop a """"""""genetic exchange"""""""" system for H. halobium. We will isolate and construct genetically marked lines of H. halobium which can be used to develop an efficient DNA transfer system such as, transformation, transduction or conjugation. Once available, a system of this type can be used to investigate the regulation of purple membrane synthesis by such classic approaches as complementation and gene fusion. In addition, a transformation and shuttle vector system is essential for the long-term goal of providing interesting site directed mutant forms of bacterio-opsin for structure and function studies. Of equal importance will be the contributions these studies will make to the virgin field of archaebacterial genetics.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM031785-06
Application #
3280102
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1983-06-01
Project End
1989-05-31
Budget Start
1988-06-01
Budget End
1989-05-31
Support Year
6
Fiscal Year
1988
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
Schools of Medicine
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
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Turner, G J; Miercke, L J; Mitra, A K et al. (1999) Expression, purification, and structural characterization of the bacteriorhodopsin-aspartyl transcarbamylase fusion protein. Protein Expr Purif 17:324-38
Gropp, F; Gropp, R; Betlach, M C (1995) Effects of upstream deletions on light- and oxygen-regulated bacterio-opsin gene expression in Halobacterium halobium. Mol Microbiol 16:357-64
Shand, R F; Betlach, M C (1994) bop gene cluster expression in bacteriorhodopsin-overproducing mutants of Halobacterium halobium. J Bacteriol 176:1655-60
Turner, G J; Miercke, L J; Thorgeirsson, T E et al. (1993) Bacteriorhodopsin D85N: three spectroscopic species in equilibrium. Biochemistry 32:1332-7
Mitra, A K; Miercke, L J; Turner, G J et al. (1993) Two-dimensional crystallization of Escherichia coli-expressed bacteriorhodopsin and its D96N variant: high resolution structural studies in projection. Biophys J 65:1295-306
Gropp, R; Gropp, F; Betlach, M C (1992) Association of the halobacterial 7S RNA to the polysome correlates with expression of the membrane protein bacterioopsin. Proc Natl Acad Sci U S A 89:1204-8
Shand, R F; Betlach, M C (1991) Expression of the bop gene cluster of Halobacterium halobium is induced by low oxygen tension and by light. J Bacteriol 173:4692-9
Thorgeirsson, T E; Milder, S J; Miercke, L J et al. (1991) Effects of Asp-96----Asn, Asp-85----Asn, and Arg-82----Gln single-site substitutions on the photocycle of bacteriorhodopsin. Biochemistry 30:9133-42
Shand, R F; Miercke, L J; Mitra, A K et al. (1991) Wild-type and mutant bacterioopsins D85N, D96N, and R82Q: high-level expression in Escherichia coli. Biochemistry 30:3082-8

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