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Chromosomal mapping of a gene affecting enterotoxin A production in Staphylococcus aureus.影响金黄色葡萄球菌肠毒素A产生的基因的染色体定位
Appl Environ Microbiol. 1982 Feb;43(2):397-402. doi: 10.1128/aem.43.2.397-402.1982.
2
Identification of a chromosomal determinant of enterotoxin A production in Staphylococcus aureus.金黄色葡萄球菌中肠毒素A产生的染色体决定因素的鉴定
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Identification of a chromosomal determinant of alpha-toxin production in Staphylococcus aureus.金黄色葡萄球菌中α-毒素产生的染色体决定因素的鉴定。
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Isolation of transposon Tn551 insertions near chromosomal markers of interest in Staphylococcus aureus.在金黄色葡萄球菌中,在感兴趣的染色体标记附近分离转座子Tn551插入片段。
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本文引用的文献

1
Identification of a chromosomal determinant of enterotoxin A production in Staphylococcus aureus.金黄色葡萄球菌中肠毒素A产生的染色体决定因素的鉴定
Appl Environ Microbiol. 1980 Jan;39(1):186-93. doi: 10.1128/aem.39.1.186-193.1980.
2
Plasmid-chromosomal transition of genes important in staphylococcal enterotoxin B expression.葡萄球菌肠毒素B表达中重要基因的质粒-染色体转变
Infect Immun. 1981 Aug;33(2):450-8. doi: 10.1128/iai.33.2.450-458.1981.
3
Distribution of Tn551 insertion sites responsible for auxotrophy on the Staphylococcus aureus chromosome.金黄色葡萄球菌染色体上导致营养缺陷型的Tn551插入位点分布。
J Bacteriol. 1981 Jan;145(1):479-88. doi: 10.1128/jb.145.1.479-488.1981.
4
Identification of a chromosomal determinant of alpha-toxin production in Staphylococcus aureus.金黄色葡萄球菌中α-毒素产生的染色体决定因素的鉴定。
Infect Immun. 1980 Oct;30(1):36-42. doi: 10.1128/iai.30.1.36-42.1980.
5
A new staphylococcal enterotoxin, enterotoxin F, associated with toxic-shock-syndrome Staphylococcus aureus isolates.一种与中毒性休克综合征金黄色葡萄球菌分离株相关的新型葡萄球菌肠毒素——肠毒素F。
Lancet. 1981 May 9;1(8228):1017-21. doi: 10.1016/s0140-6736(81)92186-3.
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Transformation analysis of three linkage groups in Staphylococcus aureus.金黄色葡萄球菌三个连锁群的转化分析
J Bacteriol. 1975 Oct;124(1):201-11. doi: 10.1128/jb.124.1.201-211.1975.
7
Genetic linkage of chromosomal tetracycline resistance and pigmentation to a purine auxotrophic marker and the isoleucine-valine-leucine structural genes in Staphylococcus aureus.金黄色葡萄球菌中染色体四环素抗性和色素沉着与嘌呤营养缺陷型标记以及异亮氨酸 - 缬氨酸 - 亮氨酸结构基因的遗传连锁。
J Bacteriol. 1976 Sep;127(3):1167-72. doi: 10.1128/jb.127.3.1167-1172.1976.
8
Staphylococcal enterotoxin A: a chromosomal gene product.葡萄球菌肠毒素A:一种染色体基因产物。
Appl Environ Microbiol. 1978 Aug;36(2):389-91. doi: 10.1128/aem.36.2.389-391.1978.
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Chromosomal map locations of integrated plasmids and related elements in Staphylococcus aureus.
Plasmid. 1977 Nov;1(1):38-51. doi: 10.1016/0147-619x(77)90007-5.
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Transformation in Staphylococcus aureus: role of bacteriophage and incidence of competence among strains.金黄色葡萄球菌的转化:噬菌体的作用及菌株中感受态的发生率
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影响金黄色葡萄球菌肠毒素A产生的基因的染色体定位

Chromosomal mapping of a gene affecting enterotoxin A production in Staphylococcus aureus.

作者信息

Mallonee D H, Glatz B A, Pattee P A

出版信息

Appl Environ Microbiol. 1982 Feb;43(2):397-402. doi: 10.1128/aem.43.2.397-402.1982.

DOI:10.1128/aem.43.2.397-402.1982
PMID:6277247
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC241838/
Abstract

In a previous study, transformation demonstrated that a gene governing enterotoxin A production (entA+) in Staphylococcus aureus strain S-6 was located on the chromosome between the purB110 and ilv-129 markers; in contrast, the entA+ gene of strain FRI-196E was shown not to be located in the same position. In the current study, 54 enterotoxin A-producing strains of S. aureus were examined to locate the entA+ gene. Conventional transformation procedures and a series of multiply marked derivatives of NCTC 8325 were used as recipients for chromosomal mapping. Of the 54 strains tested, 23 were found to contain the entA+ gene at the original locus between the purB110 and ilv-129 markers. Twenty-seven strains could not be analyzed either because their DNA was genetically ineffective in transforming strain 8325 (23 strains), or Pur+ Ilv+ transformants could not be recovered (four strains). Four other strains contained an entA+ gene that could not be located in any of the chromosomal linkage groups. A new insertion site for Tn551 was located within the hla+ gene involved in alpha-toxin production. It eliminated alpha-toxin production and was used to separate the entA+ gene from the hla+ marker in the purB110-ilv-129 region. This segment of the chromosome is shown to consist of the purB110, entA+, hla+, and ilv-129 markers in that order.

摘要

在先前的一项研究中,转化实验表明,金黄色葡萄球菌菌株S - 6中控制肠毒素A产生的基因(entA +)位于染色体上purB110和ilv - 129标记之间;相比之下,菌株FRI - 196E的entA +基因并不位于相同位置。在当前的研究中,对54株产肠毒素A的金黄色葡萄球菌菌株进行了检测,以定位entA +基因。采用常规转化程序以及NCTC 8325的一系列多重标记衍生物作为染色体定位的受体。在所检测的54株菌株中,发现有23株在purB110和ilv - 129标记之间的原始位点含有entA +基因。27株菌株无法进行分析,要么是因为它们的DNA在转化菌株8325时遗传无效(23株),要么是无法获得Pur + Ilv +转化体(4株)。另外4株菌株含有一个entA +基因,该基因无法定位在任何染色体连锁群中。Tn551的一个新插入位点位于参与α - 毒素产生的hla +基因内。它消除了α - 毒素的产生,并被用于在purB110 - ilv - 129区域将entA +基因与hla +标记分开。该染色体片段显示依次由purB110、entA +、hla +和ilv - 129标记组成。