Sequential changes in gene expression control differentiation in Bacillus subtilis during sporulation. Little information exists on the gene products of early sporulation, when rapid assembly of unique, intracellular, sporulation-specific membranes occurs, i.e. asymmetric spore septum and engulfment membranes, to establish the intracellular forespore. Dr. Andreoli has demonstrated 8 unique membrane proteins in forespore membranes and isolated genes for 4 of the 8 proteins (S1, S2, E3 and E4) by screening with specific IgG B. subtilis genomic library. Restriction maps for the cloned S1 E3, and E4 inserts were constructed. The S1, S2, E3 and E4 genes will be isolated by subcloning into lambda ZAP to locate the relevant genes in the inserts recovered from the genomic library and the genes will be mapped in the B. subtilis chromosome. The results should tell whether each of the membrane protein genes map at known spo loci, or others. %%% Current understanding of B. Subtilis molecular genetics makes this cell system ideal for studies of the control of sporulation. The early stages of this dramatic developmental change involve the rapid development of unique, intracellular, sporulation- specific membranes. This work will allow the identification of and role for some of those proteins.

Agency
National Science Foundation (NSF)
Institute
Division of Integrative Organismal Systems (IOS)
Type
Standard Grant (Standard)
Application #
8820092
Program Officer
Judith A. Verbeke
Project Start
Project End
Budget Start
1989-04-15
Budget End
1992-09-30
Support Year
Fiscal Year
1988
Total Cost
$118,000
Indirect Cost
Name
California State L a University Auxiliary Services Inc.
Department
Type
DUNS #
City
Los Angeles
State
CA
Country
United States
Zip Code
90032