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原位生成的过氧化氢在利用天然闪锌矿进行可见光驱动光催化灭活大肠杆菌中的作用:一项遗传学研究

Role of in situ resultant H₂O₂ in the visible-light-driven photocatalytic inactivation of E. coli using natural sphalerite: a genetic study.

作者信息

Shi Huixian, Huang Guocheng, Xia Dehua, Ng Tsz Wai, Yip Ho Yin, Li Guiying, An Taicheng, Zhao Huijun, Wong PoKeung

机构信息

School of Life Sciences, The Chinese University of Hong Kong , Shatin, NT, Hong Kong SAR, China.

出版信息

J Phys Chem B. 2015 Feb 19;119(7):3104-11. doi: 10.1021/jp511201w. Epub 2015 Feb 3.

Abstract

This study investigated how a natural sphalerite (NS) photocatalyst, under visible light irradiation, supports photocatalytic bacterial inactivation. This was done by comparing parent E. coli BW25113, and its two isogenic single-gene knock-out mutants, E. coli JW0797-1 (dps(-) mutant) and JW1721-1 (katE(-) mutant), where both dps and KatE genes are likely related to H2O2 production. NS could inactivate approximately 5-, 7- and 7-log of E. coli BW25113, JW0797-1, and JW1721-1 within 6 h irradiation, respectively. The two isogenic mutants were more susceptible to photocatalysis than the parental strain because of their lack of a defense system against H2O2 oxidative stress. The ability of in situ resultant H2O2 to serve as a defense against photocatalytic inactivation was also confirmed using scavenging experiments and partition system experiments. Studying catalase activity further revealed that in situ H2O2 played an important role in these inactivation processes. The destruction of bacterial cells from the cell envelope to the intracellular components was also observed using field emission-scanning electron microscopy. Moreover, FT-IR was used to monitor bacterial cell decomposition, key functional group evolution, and bacterial cell structures. This is the first study to investigate the photocatalytic inactivation mechanism of E. coli using single-gene deletion mutants under visible light irradiation.

摘要

本研究调查了天然闪锌矿(NS)光催化剂在可见光照射下如何支持光催化细菌灭活。通过比较亲本大肠杆菌BW25113及其两个同基因单基因敲除突变体大肠杆菌JW0797-1(dps(-)突变体)和JW1721-1(katE(-)突变体)来进行此项研究,其中dps和KatE基因都可能与过氧化氢的产生有关。在6小时的照射时间内,NS分别可使大肠杆菌BW25113、JW0797-1和JW1721-1的数量减少约5个对数、7个对数和7个对数。这两个同基因突变体比亲本菌株对光催化更敏感,因为它们缺乏针对过氧化氢氧化应激的防御系统。还通过清除实验和分配系统实验证实了原位产生的过氧化氢作为抵御光催化灭活的能力。进一步研究过氧化氢酶活性表明,原位过氧化氢在这些灭活过程中起重要作用。使用场发射扫描电子显微镜还观察到从细菌细胞包膜到细胞内成分的破坏。此外,傅里叶变换红外光谱用于监测细菌细胞分解、关键官能团演变和细菌细胞结构。这是第一项在可见光照射下使用单基因缺失突变体研究大肠杆菌光催化灭活机制的研究。

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