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1.
Tsitol Genet ; 50(2): 65-74, 2016.
Artigo em Russo | MEDLINE | ID: mdl-27281927

RESUMO

Strict response is a pleiotropic physiological response of cells caused by lack of aminoacetylated tRNAs. Experimentally, this response occurs due to the lack of amino acids in the environment and the limitation of tRNA aminoacylation even in the presence of the corresponding amino acids in the cell. Many features of this response indicate its dependence on the accumulation of ppGpp molecules. There is a correlation between the growth rate of actinomycetes and biosynthesis of their secondary metabolites. Introduction of additional relA gene copies of ppGpp synthetase can affect the production of antibiotics in streptomycetes. The article presents the authors' own experimental data, dedicated to the influence of heterologous relA gene expression in Streptomyces nogalater cells.


Assuntos
Actinobacteria/enzimologia , Adaptação Fisiológica , Antibióticos Antineoplásicos/biossíntese , Ligases/genética , RNA de Transferência/metabolismo , Actinobacteria/genética , Actinobacteria/crescimento & desenvolvimento , Adaptação Fisiológica/genética , Regulação Bacteriana da Expressão Gênica , Cinética , Ligases/metabolismo , Nogalamicina/biossíntese , RNA de Transferência/genética , Streptomyces/enzimologia , Streptomyces/genética
2.
Tsitol Genet ; 49(3): 9-16, 2015.
Artigo em Russo | MEDLINE | ID: mdl-26214900

RESUMO

The results of phylogenetic analysis indicate high similarity of SnoaM, SnoaL SnoaE to the cyclases involved in the biosynthesis of various antibiotics. Genes snoaM, snoaL and snoaE disruption in S. nogalater chromosome was carried on and S. nogalater MI, LI and EI strains were generated. The gene replacement events in M1, L1 and E1 were verified by Southern hybridization. Recombinant strains were characterised by lack of nogalamycin biosynthesis. Originally, M1, L1 and E1 were complemented with plasmids expressing putative cyclase genes from S. nogalater leading to restoration of nogalamycine production. The complementation results clearly indicate that obtained strains are cyclase deficient mutants. Furthermore, complementation of M1, L1 and E1 with a cyclase genes from wild-type strain is consistent with the suggested function of these enzymes.


Assuntos
Antibióticos Antineoplásicos/biossíntese , Proteínas de Bactérias/genética , Cromossomos Bacterianos , Genes Bacterianos , Isomerases/genética , Nogalamicina/biossíntese , Streptomyces/genética , Proteínas de Bactérias/metabolismo , Técnicas de Introdução de Genes , Técnicas de Silenciamento de Genes , Isomerases/deficiência , Isomerases/metabolismo , Mutagênese Insercional , Filogenia , Plasmídeos/química , Plasmídeos/metabolismo , Streptomyces/classificação , Streptomyces/metabolismo , Transformação Bacteriana
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