Cargando…

Cysteine-Mediated Extracellular Electron Transfer of Lysinibacillus varians GY32

Microbial extracellular electron transfer (EET) is essential in many natural and engineering processes. Compared with the versatile EET pathways of Gram-negative bacteria, the EET of Gram-positive bacteria has been studied much less and is mainly limited to the flavin-mediated pathway. Here, we inve...

Descripción completa

Detalles Bibliográficos
Autores principales: Kong, Guannan, Yang, Yonggang, Luo, Yeshen, Liu, Fei, Song, Da, Sun, Guoping, Li, Daobo, Guo, Jun, Dong, Meijun, Xu, Meiying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9769522/
https://www.ncbi.nlm.nih.gov/pubmed/36318024
http://dx.doi.org/10.1128/spectrum.02798-22
_version_ 1784854389073117184
author Kong, Guannan
Yang, Yonggang
Luo, Yeshen
Liu, Fei
Song, Da
Sun, Guoping
Li, Daobo
Guo, Jun
Dong, Meijun
Xu, Meiying
author_facet Kong, Guannan
Yang, Yonggang
Luo, Yeshen
Liu, Fei
Song, Da
Sun, Guoping
Li, Daobo
Guo, Jun
Dong, Meijun
Xu, Meiying
author_sort Kong, Guannan
collection PubMed
description Microbial extracellular electron transfer (EET) is essential in many natural and engineering processes. Compared with the versatile EET pathways of Gram-negative bacteria, the EET of Gram-positive bacteria has been studied much less and is mainly limited to the flavin-mediated pathway. Here, we investigate the EET pathway of a Gram-positive filamentous bacterium Lysinibacillus varians GY32. Strain GY32 has a wide electron donor spectrum (including lactate, acetate, formate, and some amino acids) in electrode respiration. Transcriptomic, proteomic, and electrochemical analyses show that the electrode respiration of GY32 mainly depends on electron mediators, and c-type cytochromes may be involved in its respiration. Fluorescent sensor and electrochemical analyses demonstrate that strain GY32 can secrete cysteine and flavins. Cysteine added shortly after inoculation into microbial fuel cells accelerated EET, showing cysteine is a new endogenous electron mediator of Gram-positive bacteria, which provides novel information to understand the EET networks in natural environments. IMPORTANCE Extracellular electron transport (EET) is a key driving force in biogeochemical element cycles and microbial chemical-electrical-optical energy conversion on the Earth. Gram-positive bacteria are ubiquitous and even dominant in EET-enriched environments. However, attention and knowledge of their EET pathways are largely lacking. Gram-positive bacterium Lysinibacillus varians GY32 has extremely long cells (>1 mm) and conductive nanowires, promising a unique and enormous role in the microenvironments where it lives. Its capability to secrete cysteine renders it not only an EET pathway to respire and survive, but also an electrochemical strategy to connect and shape the ambient microbial community at a millimeter scale. Moreover, its incapability of using flavins as an electron mediator suggests that the common electron mediator is species-dependent. Therefore, our results are important to understanding the EET networks in natural and engineering processes.
format Online
Article
Text
id pubmed-9769522
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-97695222022-12-22 Cysteine-Mediated Extracellular Electron Transfer of Lysinibacillus varians GY32 Kong, Guannan Yang, Yonggang Luo, Yeshen Liu, Fei Song, Da Sun, Guoping Li, Daobo Guo, Jun Dong, Meijun Xu, Meiying Microbiol Spectr Research Article Microbial extracellular electron transfer (EET) is essential in many natural and engineering processes. Compared with the versatile EET pathways of Gram-negative bacteria, the EET of Gram-positive bacteria has been studied much less and is mainly limited to the flavin-mediated pathway. Here, we investigate the EET pathway of a Gram-positive filamentous bacterium Lysinibacillus varians GY32. Strain GY32 has a wide electron donor spectrum (including lactate, acetate, formate, and some amino acids) in electrode respiration. Transcriptomic, proteomic, and electrochemical analyses show that the electrode respiration of GY32 mainly depends on electron mediators, and c-type cytochromes may be involved in its respiration. Fluorescent sensor and electrochemical analyses demonstrate that strain GY32 can secrete cysteine and flavins. Cysteine added shortly after inoculation into microbial fuel cells accelerated EET, showing cysteine is a new endogenous electron mediator of Gram-positive bacteria, which provides novel information to understand the EET networks in natural environments. IMPORTANCE Extracellular electron transport (EET) is a key driving force in biogeochemical element cycles and microbial chemical-electrical-optical energy conversion on the Earth. Gram-positive bacteria are ubiquitous and even dominant in EET-enriched environments. However, attention and knowledge of their EET pathways are largely lacking. Gram-positive bacterium Lysinibacillus varians GY32 has extremely long cells (>1 mm) and conductive nanowires, promising a unique and enormous role in the microenvironments where it lives. Its capability to secrete cysteine renders it not only an EET pathway to respire and survive, but also an electrochemical strategy to connect and shape the ambient microbial community at a millimeter scale. Moreover, its incapability of using flavins as an electron mediator suggests that the common electron mediator is species-dependent. Therefore, our results are important to understanding the EET networks in natural and engineering processes. American Society for Microbiology 2022-11-01 /pmc/articles/PMC9769522/ /pubmed/36318024 http://dx.doi.org/10.1128/spectrum.02798-22 Text en Copyright © 2022 Kong et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Kong, Guannan
Yang, Yonggang
Luo, Yeshen
Liu, Fei
Song, Da
Sun, Guoping
Li, Daobo
Guo, Jun
Dong, Meijun
Xu, Meiying
Cysteine-Mediated Extracellular Electron Transfer of Lysinibacillus varians GY32
title Cysteine-Mediated Extracellular Electron Transfer of Lysinibacillus varians GY32
title_full Cysteine-Mediated Extracellular Electron Transfer of Lysinibacillus varians GY32
title_fullStr Cysteine-Mediated Extracellular Electron Transfer of Lysinibacillus varians GY32
title_full_unstemmed Cysteine-Mediated Extracellular Electron Transfer of Lysinibacillus varians GY32
title_short Cysteine-Mediated Extracellular Electron Transfer of Lysinibacillus varians GY32
title_sort cysteine-mediated extracellular electron transfer of lysinibacillus varians gy32
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9769522/
https://www.ncbi.nlm.nih.gov/pubmed/36318024
http://dx.doi.org/10.1128/spectrum.02798-22
work_keys_str_mv AT kongguannan cysteinemediatedextracellularelectrontransferoflysinibacillusvariansgy32
AT yangyonggang cysteinemediatedextracellularelectrontransferoflysinibacillusvariansgy32
AT luoyeshen cysteinemediatedextracellularelectrontransferoflysinibacillusvariansgy32
AT liufei cysteinemediatedextracellularelectrontransferoflysinibacillusvariansgy32
AT songda cysteinemediatedextracellularelectrontransferoflysinibacillusvariansgy32
AT sunguoping cysteinemediatedextracellularelectrontransferoflysinibacillusvariansgy32
AT lidaobo cysteinemediatedextracellularelectrontransferoflysinibacillusvariansgy32
AT guojun cysteinemediatedextracellularelectrontransferoflysinibacillusvariansgy32
AT dongmeijun cysteinemediatedextracellularelectrontransferoflysinibacillusvariansgy32
AT xumeiying cysteinemediatedextracellularelectrontransferoflysinibacillusvariansgy32