TY  - JOUR
N1  - Copyright of this article belongs to SGM.
ID  - open650
UR  - http://mic.sgmjournals.org/content/134/5/1147.long
IS  - 5
A1  - Majumder, S
A1  - Mukhopadhyay, N K
A1  - Ghosh, S K
A1  - Bose, S K
Y1  - 1988/05//
N2  - Twelve mycobacillin-negative (My-) mutants of Bacillus subtilis B3 were isolated from an auxotrophically tagged mycobacillin producer organism. In whole-cell fermentations of some of these My- mutants a penta- and a nonapeptide accumulated; these peptides were also obtained in a cell-free system in which a new tripeptide was also detected. The amino acid composition, N- and C-terminal residues and amino acid sequence of these peptides agreed with those of equivalent segments of the mycobacillin molecule. The mycobacillin-synthesizing enzyme can be divided into three fractions that catalyse different steps in biosynthesis, and the defective enzyme fractions in the various mutant strains were identified by reconstitution experiments in vitro. The defects were further pin-pointed in mutant enzyme fractions by an ATP in equilibrium Pi exchange reaction and also by cell-free synthesis involving the use of membrane-bound enzyme. The defects so identified indicated the formation of tri-, penta- and nonapeptides as intermediates in the mycobacillin biosynthetic pathway.
PB  - Society for General Microbiology (SGM)
JF  - Journal of general microbiology
VL  - 134
SN  - 0022-1287
TI  - Genetic analysis fo the mycobacillin biosynthetic pathway in Bacillus subtilis B3.
SP  - 1147
AV  - none
EP  - 53
ER  -