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溶血链球菌、肺炎链球菌和粪肠球菌中氯霉素的耐药机制。

Resistance mechanism of chloramphenicol in Streptococcus haemolyticus, Streptococcus pneumoniae and Streptococcus faecalis.

作者信息

Miyamura S, Ochiai H, Nitahara Y, Nakagawa Y, Terao M

出版信息

Microbiol Immunol. 1977;21(2):69-76. doi: 10.1111/j.1348-0421.1977.tb02809.x.

Abstract

The chloramphenicol resistance of Streptococcus haemolyticus, Streptococcus pneumoniae and Streptococcus faecalis isolated from clinical materials was proved to be due to an inactivating enzyme produced by these bacteria. The inactivated products of chloramphenicol were identified as 1-acetoxy, 3-acetoxy and 1,3-diacetoxy derivatives by thin-layer chromatography and infrared spectroscopy. The responsible enzyme was thus confirmed to be chloramphenicol acetyltransferase. The enzyme was inducible. It was partially purified by ammonium sulfate precipitation, DEAE-cellulose chromatography and gel filtration on Sephadex G-150. The enzymes obtained from S. haemolyticus, S. pneumoniae and S. faecalis have been compared with the conclusion that they are identical with respect to molecular weight (approximately 75,000-80,000), optimum pH and heat stability.

摘要

从临床材料中分离出的溶血链球菌、肺炎链球菌和粪肠球菌对氯霉素的耐药性被证明是由于这些细菌产生的一种失活酶所致。通过薄层色谱法和红外光谱法,氯霉素的失活产物被鉴定为1-乙酰氧基、3-乙酰氧基和1,3-二乙酰氧基衍生物。因此,确认相关酶为氯霉素乙酰转移酶。该酶是可诱导的。通过硫酸铵沉淀、DEAE-纤维素色谱法和Sephadex G-150凝胶过滤对其进行了部分纯化。已对从溶血链球菌、肺炎链球菌和粪肠球菌中获得的酶进行了比较,得出的结论是,它们在分子量(约75,000-80,000)、最适pH值和热稳定性方面是相同的。

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