羟基烷酸
生物塑料
生物转化
生化工程
纳米技术
微生物
化学
材料科学
生物量(生态学)
组合化学
有机化学
细菌
废物管理
工程类
生态学
生物
发酵
遗传学
作者
Peng Zhang,Kainan Chen,Bing Xu,Jinghao Li,Cheng Hu,Joshua S. Yuan,Susie Y. Dai
出处
期刊:Chem
[Elsevier BV]
日期:2022-09-28
卷期号:8 (12): 3363-3381
被引量:52
标识
DOI:10.1016/j.chempr.2022.09.005
摘要
Integrating catalytic CO2 reduction with bioconversion could substantially advance carbon capture and utilization and mitigate climate change. However, the state-of-the-arts are limited by inefficient electron and mass transfers, unfavorable metabolic kinetics, and inadequate molecular building blocks. We overcome these barriers with the systematic design of electrocatalysis, a chemical-biological (chem-bio) interface, and microorganisms to enable efficient electro-microbial conversion with C2 (EMC2) intermediates. The soluble C2 intermediates can facilitate rapid mass transfer, readily enter primary metabolism, have less toxicity, carry more energy and electrons, and serve as better molecular building blocks for many microorganisms. The multi-tier chem-bio interface design delivered the EMC2 system to achieve 6 and 8 times increase of microbial biomass productivity compared to C1 intermediate and hydrogen-driven routes, respectively. The multi-module synthetic biology design produced medium-chain-length polyhydroxyalkanoates (PHAs), biodegradable polymers, representing much higher productivity and molecular chain length than the platforms based on C1 intermediates, hydrogen, or electrons.
科研通智能强力驱动
Strongly Powered by AbleSci AI