Journal
JOURNAL OF BACTERIOLOGY
Volume 193, Issue 10, Pages 2619-2629Publisher
AMER SOC MICROBIOLOGY
DOI: 10.1128/JB.00120-11
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Funding
- Department of Energy [DE-FG03-ER020309]
- National Science Foundation [0925126]
- Direct For Biological Sciences
- Division Of Integrative Organismal Systems [0925126] Funding Source: National Science Foundation
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The upstream intergenic regions for each of four genes encoding Ser/Thr kinases, all2334, pknE (alr3732), all4668, and all4838, were fused to a gfpmut2 reporter gene to determine their expression during heterocyst development in the cyanobacterium Anabaena (Nostoc) sp. strain PCC 7120. PpknE-gfp was upregulated after nitrogen step-down and showed strong expression in differentiating cells. Developmental regulation of pknE required a 118-bp upstream region and was abolished in a hetR mutant. A pknE mutant strain had shorter filaments with slightly higher heterocyst frequency than did the wild type. Overexpression of pknE from its native promoter inhibited heterocyst development in the wild type and in four mutant backgrounds that overproduce heterocysts. Overexpression of pknE from the copper-inducible petE promoter did not completely inhibit heterocyst development but caused a 24-h delay in heterocyst differentiation and cell bleaching 4 to 5 days after nitrogen step-down. Strains overexpressing pknE and containing PhetR-gfp or PpatS-gfp reporters failed to show developmental regulation of the reporters and had undetectable levels of HetR protein. Genetic epistasis experiments suggest that overexpression of pknE blocks HetR activity or downstream regulation.
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