Mallonee D H, Glatz B A, Pattee P A
Appl Environ Microbiol. 1982 Feb;43(2):397-402. doi: 10.1128/aem.43.2.397-402.1982.
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.
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。