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不动杆菌属菌株对新型喹诺酮类药物DW-116的耐药机制

Resistance mechanism of Acinetobacter spp. strains resistant to DW-116, a new quinolone.

作者信息

Choi K H, Baek M C, Kim B K, Choi E C

机构信息

College of Pharmacy, Seoul National University, Korea.

出版信息

Arch Pharm Res. 1998 Jun;21(3):310-4. doi: 10.1007/BF02975293.

Abstract

DW-116 is a new fluoroquinolone antimicrobial agent with a broad spectrum. In order to elucidate the resistance mechanism to DW-116 in Acinetobacter spp. bacteria, total chromosomal DNA was isolated from 10 strains of Acinetobacter spp. resistant to DW-116. Quinolone resistance determinant region (QRDR) of DNA gyrase gene was amplified by PCR. The 345 bp nucleotide fragment yielded was inserted into pKF 3 which was used as the vector. Comparisons of the DNA sequences of 8 strains with that of the wild type strain revealed a Ser-83 to Leu mutation in mutants and all ten strains contained one silent mutation(T-->G) in QRDR. From Acinetobacter MB4-8 strain, DNA gyrase was isolated and purified, through no-vobiocin-sepharose, heparin-sepharose affinity column chromatography. The enzyme was composed of two subunits and the molecular mass of subunits A and B were 75.6 and 51.9 kDa, respectively. The supercoiling activity of the reconstituted DNA gyrase composed of subunit A from Acinetobacter MB4-8 and subunit B from E. coli was not inhibited by 128 micrograms/ml of ciprofloxacin. It might be said that one of the resistance mechanisms to DW-116 in A-cinetobacter MB4-8 was subunit A alteration of DNA gyrase.

摘要

DW - 116是一种新型的广谱氟喹诺酮类抗菌剂。为了阐明不动杆菌属细菌对DW - 116的耐药机制,从10株对DW - 116耐药的不动杆菌属细菌中分离出总染色体DNA。通过聚合酶链反应(PCR)扩增DNA回旋酶基因的喹诺酮耐药决定区(QRDR)。将产生的345 bp核苷酸片段插入用作载体的pKF 3中。将8株突变株的DNA序列与野生型菌株的DNA序列进行比较,发现突变株中存在Ser - 83到Leu的突变,并且所有10株菌株在QRDR中都含有一个沉默突变(T→G)。从不动杆菌MB4 - 8菌株中,通过诺维霉素琼脂糖凝胶亲和柱色谱法和肝素琼脂糖凝胶亲和柱色谱法分离并纯化了DNA回旋酶。该酶由两个亚基组成,亚基A和B的分子量分别为75.6 kDa和51.9 kDa。由不动杆菌MB4 - 8的亚基A和大肠杆菌的亚基B组成的重组DNA回旋酶的超螺旋活性不受128微克/毫升环丙沙星的抑制。可以说,不动杆菌MB4 - 8对DW - 116的耐药机制之一是DNA回旋酶的亚基A改变。

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