期刊
MOLECULAR MICROBIOLOGY
卷 74, 期 3, 页码 724-741出版社
WILEY
DOI: 10.1111/j.1365-2958.2009.06897.x
关键词
-
资金
- German Ministry of Education and Research (BMBF) [0312834B]
P>We previously showed that the 2-oxoglutarate dehydrogenase inhibitor protein OdhI of Corynebacterium glutamicum is phosphorylated by PknG at Thr14, but that also additional serine/threonine protein kinases (STPKs) can phosphorylate OdhI. To identify these, a set of three single (Delta pknA, Delta pknB, Delta pknL), five double (Delta pknAG, Delta pknAL, Delta pknBG, Delta pknBL, Delta pknLG) and two triple deletion mutants (Delta pknALG, Delta pknBLG) were constructed. The existence of these mutants shows that PknA, PknB, PknG and PknL are not essential in C. glutamicum. Analysis of the OdhI phosphorylation status in the mutant strains revealed that all four STPKs can contribute to OdhI phosphorylation, with PknG being the most important one. Only mutants in which pknG was deleted showed a strong growth inhibition on agar plates containing glutamine as carbon and nitrogen source. Thr14 and Thr15 of OdhI were shown to be phosphorylated in vivo, either individually or simultaneously, and evidence for up to two additional phosphorylation sites was obtained. Dephosphorylation of OdhI was shown to be catalysed by the phospho-Ser/Thr protein phosphatase Ppp. Besides OdhI, the cell division protein FtsZ was identified as substrate of PknA, PknB and PknL and of the phosphatase Ppp, suggesting a role of these proteins in cell division.
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