Zobrazeno 1 - 10
of 34
pro vyhledávání: '"K F Chater"'
Publikováno v:
Scopus-Elsevier
By using a PCR approach based on conserved regions of ADP-glucose pyrophosphorylases, a glgC gene was cloned from Streptomyces coelicolor A3(2). The deduced glgC gene product showed end-to-end relatedness to other bacterial ADP-glucose pyrophosphoryl
Autor:
S D, Bentley, S, Brown, L D, Murphy, D E, Harris, M A, Quail, J, Parkhill, B G, Barrell, J R, McCormick, R I, Santamaria, R, Losick, M, Yamasaki, H, Kinashi, C W, Chen, G, Chandra, D, Jakimowicz, H M, Kieser, T, Kieser, K F, Chater
Publikováno v:
Molecular microbiology. 51(6)
The sequencing of the entire genetic complement of Streptomyces coelicolor A3(2) has been completed with the determination of the 365,023 bp sequence of the linear plasmid SCP1. Remarkably, the functional distribution of SCP1 genes somewhat resembles
Autor:
E, Takano, M, Tao, F, Long, Maureen J, Bibb, L, Wang, W, Li, M J, Buttner, Mervyn J, Bibb, Z X, Deng, K F, Chater
Publikováno v:
Molecular microbiology. 50(2)
Streptomycetes are mycelial bacteria that produce sporulating aerial hyphae on solid media. Bald (bld) mutants fail to form aerial mycelium under at least some conditions. bldA encodes the only tRNA species able to read the leucine codon UUA efficien
Publikováno v:
Molecular microbiology. 46(4)
The newly sequenced genome of Streptomyces coelicolor is estimated to encode 7825 theoretical proteins. We have mapped approximately 10% of the theoretical proteome experimentally using two-dimensional gel electrophoresis and matrix-assisted laser de
Publikováno v:
Chinese journal of biotechnology. 15(4)
A 1.3 kb DNA fragment was cloned from a total DNA library of Streptomyces ansochromogenes using Southern hybridization. Nucleotide sequencing analysis indicated that the 1320 bp DNA fragment contained a complete open reading frame (ORF). In search of
Publikováno v:
Microbiology (Reading, England). 146
The whiB sporulation gene of Streptomyces coelicolor was shown [Davis, N. K.Chater, K. F. (1992). Mol Gen Genet 232, 351-358] to encode a small, cysteine-rich putative transcription factor unlike any that had been described previously. The large data
Publikováno v:
Biochemical Society transactions. 25(4)
Publikováno v:
Biotechnology (Reading, Mass.). 28
Publikováno v:
Wei sheng wu xue bao = Acta microbiologica Sinica. 34(5)
A 1.1kb promoter P28-1 was inserted into pUC19. After then, the P28-1 was subcloned into the HindIII-EcoRI sites of the high copy number Streptomyces promoter probe plasmid pIJ4083 containing xy1E reporter gene. This recombinant plasmid was designate