The Streptomyces aureofaciens homologue of the whiB gene is essential for sporulation; its expression correlates with the developmental stage
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
10069009
DOI
10.1007/bf02816376
Knihovny.cz E-zdroje
- MeSH
- bakteriální proteiny genetika MeSH
- DNA bakterií analýza MeSH
- mapování chromozomů MeSH
- mikroskopie elektronová rastrovací MeSH
- molekulární sekvence - údaje MeSH
- plazmidy MeSH
- promotorové oblasti (genetika) MeSH
- regulace genové exprese u bakterií * MeSH
- sekvence nukleotidů MeSH
- spory bakteriální genetika MeSH
- Streptomyces aureofaciens genetika růst a vývoj ultrastruktura MeSH
- transkripční faktory genetika MeSH
- vývojová regulace genové exprese MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- bakteriální proteiny MeSH
- DNA bakterií MeSH
- transkripční faktory MeSH
- whiB protein, Streptomyces MeSH Prohlížeč
In previous experiments, a Streptomyces aureofaciens gene highly similar to the sporulation-specific whiB gene of Streptomyces coelicolor was identified. By integrative transformation, via double cross-over, a stable null mutant of the whiB-homologous gene of S. aureofaciens was obtained. The disruption blocked differentiation at a stage between the formation of aerial mycelium and the development of mature spores, producing white aerial hyphae without septation. Expression of the whiB gene was investigated during differentiation by S1 nuclease mapping, using RNA prepared from S. aureofaciens in various developmental stages. Two putative promoters were identified upstream of the whiB coding region. The stronger promoter, whiB-P2, was induced at the beginning of aerial mycelium formation, and the weaker promoter, whiB-P1, was expressed fairly constantly during differentiation. No differences in the expression of the whiB promoters were detected in an rpoZ-disrupted S. aureofaciens strain. The promoter bearing DNA fragment was inserted into the promoter-probe vector pARC1 to produce an expression pattern consistent with the results of direct RNA analysis.
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