whiH is one of several known loci specifically needed for the orderly multiple sporulation septation of aerial hyphae of Streptomyces coelicolor A3(2) and for the expression of at least some late sporulation genes. DNA complementing whiH mutants was located immediately upstream on hrdB, which encodes the principal sigma factor of S. coelicolor. Sequencing revealed a gene whose disruption gave rise to a typical whiH mutant phenotype. Four whiH mutants contained base changes or a frameshift in this gene. The deduced product of whiH related to a large family of bacterial regulatory proteins, the most similar being several repressors (such as GntR of Bacillus subtilis) responsive to carboxylate-containing intermediates in carbon metabolism. Transcription of whiH was initiated at a single promoter, PwhiH. Levels of whiH mRNA were developmentally regulated, increasing sharply when aerial mycelium was present, and reaching a maximum approximately when spores were first detectable. Transcript levels were markedly increased in a whiH mutant, indicating the possible involvement of WhiH in negative regulation of its own production. PwhiH was directly dependent on the sigma factor encoded by another sporulation gene, whiG, as shown by in vivo and in vitro transcription analysis.
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Chemosphere
January 2024
School of Mechanics and Engineering Science, Zhengzhou University, Zhengzhou 450001, China. Electronic address:
The design of semiconductor catalysts with excellent photocatalytic properties, stability, recyclability, and good separation for the treatment of polluted water is still challenging. In this paper, the ZnO/TiO nano-thin films were fabricated using the magnetron sputtering technique and then heating the underlying ZnO layer and the upper TiO layer for their respective optimal heating time, i. e.
View Article and Find Full Text PDFEnviron Technol
September 2020
Bulgаriаn Асаdеmу оf Sсiеnсеs, Institutе оf Саtаlуsis, Sоfiа, Bulgаriа.
Nоblе mеtаls suppоrtеd оn TiО (Dеgussа P25) mоdifiеd with WО undеr thе еffесt оf fееding оxуgеn аnd оzоnе соntаining mixturе tо thе rеасtоr undеr UV-С irrаdiаtiоn wеrе еxаminеd fоr thеir саtаlуtiс асtivitу in thеrеасtiоn оf оxаliс асid liquid phаsе оxidаtiоn. Thе sаmplеs wеrе sуnthеsizеd bу еxtrасtivе-pуrоlуtiс mеthоd bу lоаding 4 wt.% WО аnd 1 wt.
View Article and Find Full Text PDFMicrob Cell Fact
June 2016
Key Laboratory of Marine Drugs, Ministry of Education of China, School of Medicine and Pharmacy, Ocean University of China, Qingdao, 266003, China.
Background: Actinomycete genome sequencing has disclosed a large number of cryptic secondary metabolite biosynthetic gene clusters. However, their unavailable or limited expression severely hampered the discovery of bioactive compounds. The whiB-like (wbl) regulatory genes play important roles in morphological differentiation as well as secondary metabolism; and hence the wblA so gene was probed and set as the target to activate cryptic gene clusters in deepsea-derived Streptomyces somaliensis SCSIO ZH66.
View Article and Find Full Text PDFAntonie Van Leeuwenhoek
July 2015
School of Chemical and Biological Engineering and Institute of Molecular Biology and Genetics, Seoul National University, Kwanak-gu, Seoul, 151-744, Korea.
SsgA-like proteins are a family of actinomycete-specific regulatory proteins that control cell division and spore maturation in streptomycetes. SsgA and SsgB together activate sporulation-specific cell division by controlling the localization of FtsZ. Here we report the identification of novel regulators that control the transcription of the ssgA-like genes.
View Article and Find Full Text PDFAppl Environ Microbiol
November 2014
College of Life Sciences, Zhejiang University, Hangzhou, China Key Laboratory of Microbial Biochemistry and Metabolism Engineering of Zhejiang Province, Hangzhou, China
Detailed mechanisms of WhiB-like (Wbl) proteins involved in antibiotic biosynthesis and morphological differentiation are poorly understood. Here, we characterize the role of WblAch, a Streptomyces chattanoogensis L10 protein belonging to this superfamily. Based on DNA microarray data and verified by real-time quantitative PCR (qRT-PCR), the expression of wblAch was shown to be positively regulated by AdpAch.
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