Suppr超能文献

肺炎双球菌突变型和野生型黄递酶的纯化及性质

Purification and properties of mutant and wild-type diaphorases from Diplococcus pneumoniae.

作者信息

Kreger A S, Olsen R H

出版信息

J Bacteriol. 1968 Oct;96(4):1029-36. doi: 10.1128/jb.96.4.1029-1036.1968.

Abstract

Optochin-resistant mutant and wild-type diaphorases were purified approximately 300-fold by a combination of batch adsorption and column chromatography with diethylaminoethyl cellulose, and were characterized with regard to their pH optima, sensitivity to optochin inhibition and heat inactivation, Michaelis constants with flavine mononucleotide (FMN) and reduced nicotinamide adenine dinucleotide (NADH), and inhibition constants with optochin hydrochloride. The pH optima of the purified diaphorases were similar, but the purified diaphorases from the optochin-resistant strains were approximately four to five times more resistant to heat inactivation at 45 C than was the wild-type diaphorase. Purified diaphorase preparations from the optochin-resistant pneumococci had greater activities per milligram of protein and were more resistant to optochin inhibition than the preparation from the optochin-sensitive pneumococcus. Michaelis constants for FMN and NADH were similar; however, the inhibition constants of the optochin-resistant diaphorases were four to eight times greater than that of the optochin-sensitive diaphorase. Optochin hydrochloride produced a noncompetitive type of inhibition with FMN as substrate but a competitive type of inhibition with NADH as substrate. Optochin hydrochloride produced an approximately 10-fold increase in the Michaelis constant for NADH. The concentration of drug required to produce this effect was, however, greater with the mutant diaphorases than with the wild-type diaphorase. Optochin hydrochloride quenched the fluorescence of riboflavine. This phenomenon did not appear to be related to the diaphorase-inhibitory activity of the drug, however, since the pH requirements of the two reactions were different. Quenching of riboflavine fluorescence by optochin hydrochloride increased with a rise in pH, whereas inhibition of diaphorase activity by optochin hydrochloride was greater at pH 6.8 than at pH 7.6.

摘要

通过分批吸附和二乙氨基乙基纤维素柱色谱相结合的方法,将对奥普托欣耐药的突变体和野生型黄递酶纯化了约300倍,并对其pH最适值、对奥普托欣抑制和热失活的敏感性、与黄素单核苷酸(FMN)和还原型烟酰胺腺嘌呤二核苷酸(NADH)的米氏常数以及与盐酸奥普托欣的抑制常数进行了表征。纯化的黄递酶的pH最适值相似,但来自奥普托欣耐药菌株的纯化黄递酶在45℃下对热失活的耐受性比野生型黄递酶高约四到五倍。来自奥普托欣耐药肺炎球菌的纯化黄递酶制剂每毫克蛋白质具有更高的活性,并且比来自奥普托欣敏感肺炎球菌的制剂对奥普托欣抑制更具耐受性。FMN和NADH的米氏常数相似;然而,奥普托欣耐药黄递酶的抑制常数比奥普托欣敏感黄递酶的抑制常数大四到八倍。盐酸奥普托欣以FMN为底物时产生非竞争性抑制类型,但以NADH为底物时产生竞争性抑制类型。盐酸奥普托欣使NADH的米氏常数增加了约10倍。然而,产生这种效应所需的药物浓度,突变体黄递酶比野生型黄递酶更高。盐酸奥普托欣淬灭了核黄素的荧光。然而,这种现象似乎与药物的黄递酶抑制活性无关,因为两个反应的pH要求不同。盐酸奥普托欣对核黄素荧光的淬灭随着pH的升高而增加,而盐酸奥普托欣对黄递酶活性的抑制在pH 6.8时比在pH 7.6时更强。

相似文献

4
Diaphorases from Aerobacter aerogenes.产气气杆菌的黄递酶
J Bacteriol. 1966 Nov;92(5):1404-14. doi: 10.1128/jb.92.5.1404-1414.1966.
7
Purification and characterization of diaphorases from some Drosophila species.
Biochem Genet. 1992 Jun;30(5-6):305-15. doi: 10.1007/BF02396219.

本文引用的文献

8
Diaphorases from Aerobacter aerogenes.产气气杆菌的黄递酶
J Bacteriol. 1966 Nov;92(5):1404-14. doi: 10.1128/jb.92.5.1404-1414.1966.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验