{"title":"Engineering Microbial Consortium Biohybrid System to Efficiently Produce Electricity from Lignocellulose Biomass.","authors":"Junqi Zhang, Yuanxiu Li, Wenjing Lv, Zixuan You, Huan Yu, Baocai Zhang, Qijing Liu, Jing Zou, Tao Chen, Feng Li, Hao Song","doi":"10.1021/acssynbio.5c00178","DOIUrl":null,"url":null,"abstract":"<p><p>Converting lignocellulose into bioelectricity through a bioelectrocatalytic system (BES) has emerged as a promising approach to addressing environmental pollution and energy regeneration challenges. However, practical application of BES is significantly constrained by the fact that the electroactive biocatalyst <i>Shewanella oneidensis</i> lacks the essential metabolic pathways and enzymes required for utilizing lignocellulose for cell growth and power generation. Here, to realize clean electricity production from lignocellulose hydrolysate, an artificial microbial consortium comprising <i>S. oneidensis</i>, <i>Lactococcus lactis</i>, and <i>Bacillus subtilis</i> was developed. In this consortium, <i>L. lactis</i> is responsible for converting glucose into lactate; <i>B. subtilis</i> metabolizes glucose and xylose into riboflavin; and <i>S. oneidensis</i> then employs lactate as an electron donor and riboflavin as an electron shuttle to facilitate electricity generation. Subsequently, to increase substrate conversion efficiency of the microbial consortium, three key genes <i>codY</i>, <i>ribA</i>, and <i>dld</i> encoding lactate dehydrogenase, GTP cyclohydrolase, and d-lactate dehydrogenase, were expressed in <i>L. lactis</i>, <i>B. subtilis</i>, and <i>S. oneidensis</i>, respectively, which accelerated glucose-to-lactate conversion, riboflavin synthesis, and lactate metabolism. Also, to accelerate the extracellular electron transfer (EET) capacity of the microbial consortium, the <i>cyc2</i> gene from <i>Acidithiobacillus ferrooxidans</i> encoding the outer membrane <i>c</i>-type cytochrome was further expressed in <i>S. oneidensis</i>. Finally, to further enhance the interfacial EET capability of the microbial consortium, a 3D microbiota biohybrid system <i>S</i><sub>7</sub><i>L</i><sub>1</sub><i>B</i><sub>1</sub>@CF&GO consisting of carbon felts and graphene oxide was developed to reduce the internal resistance of BES. The results showed that the artificial biohybrid system could obtain a maximum power density of ∼739.40 mW m<sup>-2</sup> using lignocellulosic hydrolysate as the carbon source. This system expands the range of carbon sources available to <i>S. oneidensis</i> for efficient power generation from the lignocellulosic hydrolysate.</p>","PeriodicalId":26,"journal":{"name":"ACS Synthetic Biology","volume":" ","pages":"2305-2315"},"PeriodicalIF":3.7000,"publicationDate":"2025-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Synthetic Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1021/acssynbio.5c00178","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/5 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0
Abstract
Converting lignocellulose into bioelectricity through a bioelectrocatalytic system (BES) has emerged as a promising approach to addressing environmental pollution and energy regeneration challenges. However, practical application of BES is significantly constrained by the fact that the electroactive biocatalyst Shewanella oneidensis lacks the essential metabolic pathways and enzymes required for utilizing lignocellulose for cell growth and power generation. Here, to realize clean electricity production from lignocellulose hydrolysate, an artificial microbial consortium comprising S. oneidensis, Lactococcus lactis, and Bacillus subtilis was developed. In this consortium, L. lactis is responsible for converting glucose into lactate; B. subtilis metabolizes glucose and xylose into riboflavin; and S. oneidensis then employs lactate as an electron donor and riboflavin as an electron shuttle to facilitate electricity generation. Subsequently, to increase substrate conversion efficiency of the microbial consortium, three key genes codY, ribA, and dld encoding lactate dehydrogenase, GTP cyclohydrolase, and d-lactate dehydrogenase, were expressed in L. lactis, B. subtilis, and S. oneidensis, respectively, which accelerated glucose-to-lactate conversion, riboflavin synthesis, and lactate metabolism. Also, to accelerate the extracellular electron transfer (EET) capacity of the microbial consortium, the cyc2 gene from Acidithiobacillus ferrooxidans encoding the outer membrane c-type cytochrome was further expressed in S. oneidensis. Finally, to further enhance the interfacial EET capability of the microbial consortium, a 3D microbiota biohybrid system S7L1B1@CF&GO consisting of carbon felts and graphene oxide was developed to reduce the internal resistance of BES. The results showed that the artificial biohybrid system could obtain a maximum power density of ∼739.40 mW m-2 using lignocellulosic hydrolysate as the carbon source. This system expands the range of carbon sources available to S. oneidensis for efficient power generation from the lignocellulosic hydrolysate.
期刊介绍:
The journal is particularly interested in studies on the design and synthesis of new genetic circuits and gene products; computational methods in the design of systems; and integrative applied approaches to understanding disease and metabolism.
Topics may include, but are not limited to:
Design and optimization of genetic systems
Genetic circuit design and their principles for their organization into programs
Computational methods to aid the design of genetic systems
Experimental methods to quantify genetic parts, circuits, and metabolic fluxes
Genetic parts libraries: their creation, analysis, and ontological representation
Protein engineering including computational design
Metabolic engineering and cellular manufacturing, including biomass conversion
Natural product access, engineering, and production
Creative and innovative applications of cellular programming
Medical applications, tissue engineering, and the programming of therapeutic cells
Minimal cell design and construction
Genomics and genome replacement strategies
Viral engineering
Automated and robotic assembly platforms for synthetic biology
DNA synthesis methodologies
Metagenomics and synthetic metagenomic analysis
Bioinformatics applied to gene discovery, chemoinformatics, and pathway construction
Gene optimization
Methods for genome-scale measurements of transcription and metabolomics
Systems biology and methods to integrate multiple data sources
in vitro and cell-free synthetic biology and molecular programming
Nucleic acid engineering.