A ketoreductase gene from Streptomyces mycarofaciens 1748 DNA involved in biosynthesis of a spore pigment

被引:0
作者
夏焕章
王以光
机构
[1] InstituteofMedicinalBiotechnology,ChineseAcademyofMedicalSciences,PekingUnionofMedicalCollege,Beijing,China,InstituteofMedicinalBiotechnology,ChineseAcademyofMedicalSciences,PekingUnionofMedicalCollege,Beijing,China
关键词
gene disruption; spore pigment; ketoreductase; midecamycin;
D O I
暂无
中图分类号
Q75 [分子遗传学];
学科分类号
071007 ;
摘要
<正> An efficient plasmid transformation system for S. mycarofaciens 1748 has been established. In order to determine the function of MKR gene in S. mycarofaciens 1748, the gene disruption experiment was carried out. For this purpose the plasmid pKC1139 was used. A recombinant strain with white spore appeared, in contrast to the grey-colour spore of S. mycarofaciens 1748. This suggested that homologous recombination between plasmid-borne MKR gene sequence and the chromosome of S. mycarofaciens 1748 had occurred. A Southern hybridization experiment using α- P-labelled MKR gene as probe indicated that the desired integration event had occurred in the re-combinant. The result of gene disruption showed that the alteration of this gene in the chromosome of S. mycarofa-ciens 1748 made sporulating colonies remain white instead of taking on the typical grey colour of sporulating wild type colonies, suggesting that MKR gene is involved in the biosynthesis of a spore pigment. The recombinant strain was in-cubated wit
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页码:636 / 641
页数:6
相关论文
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[1]  
Characterisation of act I-homologous DNA encoding polyketide synthase genes from the monensin producer Streptomyces cinnamonensis[J] . Teresa J. Arrowsmith,Francisco Malpartida,David H. Sherman,Ashley Birch,David A. Hopwood,John A. Robinson.MGG Molecular & General Genetics . 1992 (2)