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DNA rearrangements associated with instability of an arginine gene in Streptomyces coelicolor A3(2).

作者信息

Flett F, Platt J, Cullum J

出版信息

J Basic Microbiol. 1987;27(1):3-10. doi: 10.1002/jobm.3620270102.

DOI:10.1002/jobm.3620270102
PMID:3598876
Abstract

Streptomyces coelicolor A3(2) gives rise to spontaneous chloramphenicol sensitive mutants at a frequency of about 0.3% per spore. These mutants are often genetically unstable and give rise to arginine auxotrophs (Arg-) at frequencies of 1-7% per spore. These Arg- mutants usually lack the enzyme argininosuccinate synthetase (one exception was found that lacked ornithine carbamoyltransferase) and were shown to have deleted the corresponding argG gene by hybridisation analysis using a cloned S. cattleya argG gene. The Arg- strains also showed a variety of different DNA amplification and deletion events in a region homologous to an amplified DNA sequence found in spontaneous Arg- mutants in S. lividans 66.

摘要

相似文献

1
DNA rearrangements associated with instability of an arginine gene in Streptomyces coelicolor A3(2).
J Basic Microbiol. 1987;27(1):3-10. doi: 10.1002/jobm.3620270102.
2
Relationship of an unstable argG gene to a 5.7-kilobase amplifiable DNA sequence in Streptomyces lividans 66.
J Bacteriol. 1987 Oct;169(10):4804-10. doi: 10.1128/jb.169.10.4804-4810.1987.
3
DNA deletions in spontaneous chloramphenicol-sensitive mutants of Streptomyces coelicolor A 3(2) and Streptomyces lividans 66.天蓝色链霉菌A 3(2)和变铅青链霉菌66自发氯霉素敏感突变体中的DNA缺失
Mol Gen Genet. 1987 May;207(2-3):499-502. doi: 10.1007/BF00331621.
4
DNA amplification and an unstable arginine gene in Streptomyces lividans 66.天蓝色链霉菌66中的DNA扩增与一个不稳定的精氨酸基因
Mol Gen Genet. 1984;195(1-2):134-8. doi: 10.1007/BF00332735.
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argJ mutations are highly inducible by ethidium bromide in proB strains of Streptomyces lividans: implication of pathway interactions.在淡紫灰链霉菌的proB菌株中,argJ突变可被溴化乙锭高度诱导:途径相互作用的影响
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6
The argG gene of Streptomyces clavuligerus has low homology to unstable argG from other actinomycetes: effect of amplification on clavulanic acid biosynthesis.棒状链霉菌的argG基因与其他放线菌的不稳定argG基因具有低同源性:扩增对克拉维酸生物合成的影响。
Gene. 1995 Dec 29;167(1-2):9-15. doi: 10.1016/0378-1119(95)00667-2.
7
Genetic instability and DNA amplification in Streptomyces lividans 66.变铅青链霉菌66中的遗传不稳定性和DNA扩增
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8
Structure of an amplifiable DNA sequence in Streptomyces lividans 66.
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9
[Amplifying sequences in the Streptomyces coelicolor A3 (2) gene].
Antibiot Khimioter. 1990 Dec;35(12):21-3.
10
Structural organization, amplification, deletion and rearrangements of DNA sequences associated with an unstable region of the chromosome of Streptomyces coelicolor A3(2).与天蓝色链霉菌A3(2)染色体不稳定区域相关的DNA序列的结构组织、扩增、缺失及重排
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引用本文的文献

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Mutational meltdown of putative microbial altruists in Streptomyces coelicolor colonies.假定微生物利他主义者在链霉菌群体中的突变崩溃。
Nat Commun. 2022 Apr 27;13(1):2266. doi: 10.1038/s41467-022-29924-y.
2
Genome-scale analysis of Streptomyces coelicolor A3(2) metabolism.天蓝色链霉菌A3(2)代谢的全基因组规模分析。
Genome Res. 2005 Jun;15(6):820-9. doi: 10.1101/gr.3364705.
3
Implication of a repression system, homologous to those of other bacteria, in the control of arginine biosynthesis genes in Streptomyces coelicolor.
一种与其他细菌的阻遏系统同源的阻遏系统在天蓝色链霉菌精氨酸生物合成基因控制中的作用。
Mol Gen Genet. 1996 May 23;251(2):245-51. doi: 10.1007/BF02172924.
4
DNA amplification affects protease production and sporulation in Streptomyces fradiae.DNA扩增影响弗氏链霉菌中蛋白酶的产生和孢子形成。
Curr Microbiol. 1994 Aug;29(2):101-7. doi: 10.1007/BF01575756.
5
DNA deletions in spontaneous chloramphenicol-sensitive mutants of Streptomyces coelicolor A 3(2) and Streptomyces lividans 66.天蓝色链霉菌A 3(2)和变铅青链霉菌66自发氯霉素敏感突变体中的DNA缺失
Mol Gen Genet. 1987 May;207(2-3):499-502. doi: 10.1007/BF00331621.
6
Extremely large chromosomal deletions are intimately involved in genetic instability and genomic rearrangements in Streptomyces glaucescens.极大型染色体缺失与浅绿链霉菌的遗传不稳定性和基因组重排密切相关。
Mol Gen Genet. 1989 Jun;217(2-3):447-58. doi: 10.1007/BF02464916.
7
Heterogeneous genomic amplification in Streptomyces glaucescens: structure, location and junction sequence analysis.浅绿链霉菌中的异质基因组扩增:结构、定位及连接序列分析
Mol Gen Genet. 1989 Jun;217(2-3):437-46. doi: 10.1007/BF02464915.