Naradasu Divya, Miran Waheed, Sakamoto Mitsuo, Okamoto Akihiro
International Center for Materials Nanoarchitectonics (WPI-MANA), National Institute for Materials Science, Tsukuba, Japan.
Department of Advanced Interdisciplinary Studies, Research Center for Advanced Science and Technology, Graduate School of Engineering, The University of Tokyo, Tokyo, Japan.
Front Microbiol. 2019 Jan 15;9:3267. doi: 10.3389/fmicb.2018.03267. eCollection 2018.
Microorganisms are known to exhibit extracellular electron transfer (EET) in a wide variety of habitats. However, as for the human microbiome which significantly impacts our health, the role and importance of EET has not been widely investigated. In this study, we enriched and isolated the EET-capable bacteria from human gut microbes using an electrochemical enrichment method and examined whether the isolates couple EET with anaerobic respiration or fermentation. Upon the use of energy-rich or minimum media (with acetate or lactate) for electrochemical enrichment with the human gut sample at an electrode potential of +0.4 V [vs. the standard hydrogen electrode (SHE)], both culture conditions showed significant current production. However, EET-capable pure strains were enriched specifically with minimum media, and subsequent incubation using the δ-MnO-agar plate with lactate or acetate led to the isolation of two EET-capable microbial strains, and , having 99% of 16S rRNA gene sequence identity with () and (), respectively. While the enrichment involved anaerobic respiration with acetate and lactate, further electrochemistry with and revealed that the glucose fermentation was also coupled with EET. These results indicate that EET couples not only with anaerobic respiration as found in environmental bacteria, but also with fermentation in the human gut.
众所周知,微生物在各种各样的栖息地中都能进行细胞外电子转移(EET)。然而,对于对我们的健康有重大影响的人类微生物群而言,EET的作用和重要性尚未得到广泛研究。在本研究中,我们使用电化学富集方法从人类肠道微生物中富集并分离出具有EET能力的细菌,并研究这些分离株是否将EET与无氧呼吸或发酵联系起来。在使用富含能量的培养基或基本培养基(含乙酸盐或乳酸盐),以+0.4 V的电极电位[相对于标准氢电极(SHE)]对人类肠道样本进行电化学富集时,两种培养条件均显示出显著的电流产生。然而,具有EET能力的纯菌株是通过基本培养基特异性富集的,随后使用含乳酸盐或乙酸盐的δ-MnO琼脂平板进行培养,从而分离出两种具有EET能力的微生物菌株,分别与()和()的16S rRNA基因序列具有99%的同一性。虽然富集过程涉及乙酸盐和乳酸盐的无氧呼吸,但对和进行的进一步电化学研究表明,葡萄糖发酵也与EET相关联。这些结果表明,EET不仅如在环境细菌中那样与无氧呼吸相关联,而且在人类肠道中还与发酵相关联。