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Krebs cycle function is required for activation of the Spo0A transcription factor in Bacillus subtilis.
Author(s) -
Keith Ireton,
Shijie Jin,
A D Grossman,
Abraham L. Sonenshein
Publication year - 1995
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.92.7.2845
Subject(s) - bacillus subtilis , citric acid cycle , biology , transcription factor , mutant , biochemistry , transcription (linguistics) , microbiology and biotechnology , sigma factor , gene , signal transduction , enzyme , phosphorylation , regulation of gene expression , gene expression , genetics , promoter , bacteria , linguistics , philosophy
Expression of genes early during sporulation in Bacillus subtilis requires the activity of the transcription factor encoded by spo0A. The active, phosphorylated form of Spo0A is produced through the action of a multicomponent pathway, the phosphorelay. A mutant defective in the first three enzymes of the Krebs citric acid cycle was unable to express early sporulation genes, apparently because of a failure to activate the phosphorelay. Cells that produce an altered Spo0A protein that can be phosphorylated by an alternative pathway were not dependent on Krebs cycle function for early sporulation gene expression. These findings suggest that Krebs cycle enzymes transmit a signal to activate the phosphorelay and that B. subtilis monitors its metabolic potential before committing itself to spore formation.

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