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寻找针对致病性幽门螺杆菌和弯曲杆菌菌株的有效且特异的抗生素。

Searching for potent and specific antibiotics against pathogenic Helicobacter and Campylobacter strains.

机构信息

Graduate School of Engineering, Hokkaido University, N13 & W8, Kita-ku, Sapporo, Hokkaido, 060-8628, Japan.

出版信息

J Ind Microbiol Biotechnol. 2019 Mar;46(3-4):409-414. doi: 10.1007/s10295-018-2108-3. Epub 2018 Nov 20.

Abstract

Menaquinone is an obligatory component of the electron-transfer pathway in microorganisms. Its biosynthetic pathway was established by pioneering studies with Escherichia coli and it was revealed to be derived from chorismate by Men enzymes. However, we identified an alternative pathway, the futalosine pathway, operating in some microorganisms including Helicobacter pylori and Campylobacter jejuni, which cause gastric carcinoma and diarrhea, respectively. Because some useful intestinal bacteria, such as lactobacilli, use the canonical pathway, the futalosine pathway is an attractive target for development of chemotherapeutics for the abovementioned pathogens. In this mini-review, we summarize compounds that inhibit Mqn enzymes involved in the futalosine pathway discovered to date.

摘要

甲萘醌是微生物中电子传递途径的必需组成部分。其生物合成途径是通过对大肠杆菌的开创性研究确立的,结果表明它是由甲萘醌酶从分支酸衍生而来的。然而,我们在包括导致胃癌的幽门螺杆菌和引起腹泻的空肠弯曲菌在内的一些微生物中发现了一种替代途径,即呋咱甲萘醌途径。因为一些有益的肠道细菌,如乳杆菌,使用经典途径,所以呋咱甲萘醌途径是开发针对上述病原体的化学疗法的有吸引力的靶标。在这篇综述中,我们总结了迄今为止发现的抑制参与呋咱甲萘醌途径的 Mqn 酶的化合物。

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