Nisin and subtilin are peptide antibiotics that are synthesized ribosomally and converted to mature active forms by post-transcriptional modifications. Because their structures are gene-encoded, they are amenable to controlled structural modification by mutagenesis. The powerful tools of genetic engineering can therefore by used to construct new forms of these antibiotics with novel and useful properties, that may help alleviate the growing problem of antibiotic resistance in bacterial populations; which is steadily reducing our arsenal of useful antibacterial agents. The structural gene for subtilin has recently been cloned in Bacillus subtilis by workers in this laboratory. With the gene available for the first time, it will be possible to study the structure and organization of the subtilin structural genes, and the structure and organization of the subtilin structural genes, and the peptide precursor from which subtilin is made. The precursor can be used to test hypotheses about the biosynthetic pathway for subtilin. Our results from restriction mapping of cloned subtilin genes suggest they may be in a transposon, that may also encode the post-transcriptional processing enzymes. This hypothesis will be tested by transferring the genetic element to a non-subtilin producing strain, and looking for subtilin production. If this is successful, the nucleic acid sequence will be studied in detail. Also, we will attempt to construct an expression system that will produce the antibiotic more efficiently than is now possible. We have evidence that the dehydro residues in nisin are bifunctional; one reacting with membrane sulfhydryl groups and another acting to """"""""anchor"""""""" the antibiotic to the cell surface. This will be studied further by incorporation studies of radioactive nisin that has been synthesized in vivo from labeled precursors.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI024454-02
Application #
3137462
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1987-04-01
Project End
1990-03-31
Budget Start
1988-04-01
Budget End
1989-03-31
Support Year
2
Fiscal Year
1988
Total Cost
Indirect Cost
Name
University of Maryland College Park
Department
Type
Earth Sciences/Resources
DUNS #
City
College Park
State
MD
Country
United States
Zip Code
20742
Chakicherla, Anu; Ecale Zhou, Carol L; Dang, Martha Ligon et al. (2009) SpaK/SpaR two-component system characterized by a structure-driven domain-fusion method and in vitro phosphorylation studies. PLoS Comput Biol 5:e1000401
Yuksel, Sahru; Hansen, J Norman (2007) Transfer of nisin gene cluster from Lactococcus lactis ATCC 11454 into the chromosome of Bacillus subtilis 168. Appl Microbiol Biotechnol 74:640-9
Buchman, G W; Banerjee, S; Hansen, J N (1988) Structure, expression, and evolution of a gene encoding the precursor of nisin, a small protein antibiotic. J Biol Chem 263:16260-6