M. Marino et al., Changes in protein synthesis during the adaptation of Bacillus subtilis toanaerobic growth conditions, MICROBIO-UK, 146, 2000, pp. 97-105
After a shift of Bacillus subtilis from aerobic to anaerobic growth conditi
ons, nitrate ammonification and various fermentative processes replace oxyg
en-dependent respiration. Cell-free extracts prepared from wild-type a. sub
tilis and from mutants of the regulatory loci fnr and resDE grown under aer
obic and various anaerobic conditions were compared by two-dimensional gel
electrophoresis. Proteins involved in the adaptation process were identifie
d by their N-terminal sequence. Induction of cytoplasmic lactate dehydrogen
ase (LctE) synthesis under anaerobic fermentative conditions was dependent
on fnr and resDE. Anaerobic nitrate repression of LctE formation required f
nr-mediated expression of narGHJI, encoding respiratory nitrate reductase,
Anaerobic induction of the flavohaemoglobin Hmp required resDE and nitrite.
The general anaerobic induction of ywfl, encoding a protein of unknown Ine
general anaerobic induction or ywfl, encoding a protien or unknown functio
n, was modulated by resDE and fnr, The ywfl gene shares its upstream region
with the pta gene, encoding the fermentative enzyme acetyl-CoA:orthophosph
ate acetyltransferase. Anaerobic repression of the synthesis of a potential
membrane-associated NADH dehydrogenase (YjlD, Ndh), and anaerobic inductio
n of fructose-1,6-bisphosphate aldolase (FbaA) and dehydrolipoamide dehydro
genase (PhdD, Lpd) formation, did not require fnr or resDE participation. S
ynthesis of glycerol kinase (GlpK) was decreased under anaerobic conditions
. Finally, the effect of anaerobic stress induced by the immediate shift fr
om aerobic to strictly anaerobic conditions was analysed. The induction of
various systems for the utilization of alternative carbon sources such as i
nositol (lolA, lolC, lolH, loll), melibiose (MelA) and 6-phospho-alpha-gluc
osides (GlvA) indicated a catabolite-response-like stress reaction.