Kurihara Shin
Faculty of Biology-Oriented Science and Technology, Kindai University, Kinokawa, Wakayama 649-6493, Japan.
Biosci Microbiota Food Health. 2021;40(1):19-26. doi: 10.12938/bmfh.2020-011. Epub 2020 Sep 10.
Comparisons of the changes in the gut microbiota and transcriptomes as a result of changes in diet have demonstrated that the regulation of the gene functions of intestinal bacteria is fundamental for the regulation of the intestinal environment. However, the functions of only about half of the genes can be predicted using nucleotide sequences obtained from the metagenomic data of the human gut microbiota. Therefore, the regulation of gut bacterial gene functions is hindered. To resolve this issue, the functions of the genes of intestinal bacteria must be identified. In our previous study, a high-throughput cultivation system was established for the dominant species of indigenous human intestinal microbiota. Using this system, we analyzed the synthesis and transport of polyamines by intestinal bacteria. Comparison of the results with those obtained by analysis indicated the existence of novel polyamine synthetic enzymes and transport proteins. Next, strains with gene deletions and complementation for the polyamine synthetic system of the genus were analyzed. Furthermore, we co-cultured genetically engineered and strains to demonstrate the presence of a polyamine synthetic pathway spanning multiple bacterial species. Here, we outline the trends of research using genetically engineered intestinal bacteria and the ripple effects of studies in which intestinal bacteria have been analyzed genetically. Moreover, because studies on intestinal bacteria at the gene level are indispensable for improving our understanding of their regulation, the importance of this research will continue to increase in the future.
对饮食变化导致的肠道微生物群和转录组变化的比较表明,肠道细菌基因功能的调节对于肠道环境的调节至关重要。然而,利用从人类肠道微生物群的宏基因组数据获得的核苷酸序列,只能预测大约一半基因的功能。因此,肠道细菌基因功能的调节受到阻碍。为了解决这个问题,必须确定肠道细菌基因的功能。在我们之前的研究中,为人类本土肠道微生物群的优势物种建立了一个高通量培养系统。利用这个系统,我们分析了肠道细菌中多胺的合成和运输。将结果与通过分析获得的结果进行比较,表明存在新的多胺合成酶和转运蛋白。接下来,分析了该属多胺合成系统基因缺失和互补的菌株。此外,我们对基因工程改造的和菌株进行了共培养,以证明存在跨越多个细菌物种的多胺合成途径。在这里,我们概述了使用基因工程改造的肠道细菌的研究趋势以及对肠道细菌进行基因分析的研究的连锁反应。此外,由于在基因水平上对肠道细菌的研究对于增进我们对其调节的理解不可或缺,这项研究的重要性在未来将持续增加。