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Analysis of putative DNA amplification genes in the element AUD1 of Streptomyces lividans 66.

作者信息

Piendl W, Eichenseer C, Viel P, Altenbuchner J, Cullum J

机构信息

Institut für medizinische Chemie und Biochemie, Universität Innsbruck, Austria.

出版信息

Mol Gen Genet. 1994 Aug 15;244(4):439-43. doi: 10.1007/BF00286697.

DOI:10.1007/BF00286697
PMID:8078470
Abstract

The amplifiable AUD1 element of Streptomyces lividans 66 consists of two copies of a 4.7 kb sequence flanked by three copies of a 1 kb sequence. The DNA sequences of the three 1 kb repeats were determined. Two copies (left and middle repeats) were identical: (1009 bp in length) and the right repeat was 1012 bp long and differed at 63 positions. The repeats code for open reading frames (ORFs) with typical Streptomyces codon usage, which would encode proteins of about 36 kD molecular weight. The sequences of these ORFs suggest that they specify DNA-binding proteins and potential palindromic binding sites are found adjacent to the genes. The putative amplification protein encoded by the right repeat was expressed in Escherichia coli.

摘要

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本文引用的文献

1
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J Bacteriol. 1993 Jun;175(11):3422-9. doi: 10.1128/jb.175.11.3422-3429.1993.
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The Streptomyces lividans 66 chromosome contains a 1 MB deletogenic region flanked by two amplifiable regions.
Mol Gen Genet. 1993 Nov;241(3-4):255-62. doi: 10.1007/BF00284676.
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The chromosomal DNA of Streptomyces lividans 66 is linear.变铅青链霉菌66的染色体DNA是线性的。
天蓝色链霉菌中的淀粉酶和几丁质酶基因受reg1调控,reg1是一个多效调控基因。
J Bacteriol. 1997 Oct;179(20):6383-90. doi: 10.1128/jb.179.20.6383-6390.1997.
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Influence of disruption of the recA gene on genetic instability and genome rearrangement in Streptomyces lividans.recA基因破坏对淡紫链霉菌遗传不稳定性和基因组重排的影响。
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The very large amplifiable element AUD2 from Streptomyces lividans 66 has insertion sequence-like repeats at its ends.来自变铅青链霉菌66的非常大的可扩增元件AUD2在其末端具有类似插入序列的重复序列。
J Bacteriol. 1994 Nov;176(22):7107-12. doi: 10.1128/jb.176.22.7107-7112.1994.
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A comprehensive set of sequence analysis programs for the VAX.一套适用于VAX的综合序列分析程序。
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