4.7 Review

Bio-valorization of C1 gaseous substrates into bioalcohols: Potentials and challenges in reducing carbon emissions

Journal

BIOTECHNOLOGY ADVANCES
Volume 59, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.biotechadv.2022.107954

Keywords

C1 gaseous substrates; Bioconversion; Alcohol biosynthesis; Metabolic engineering; Process development

Funding

  1. National Key R&D Programs of China [2018YFA0901500]
  2. National Natural Science Foundation of China [21878241, 22178281, 22108219]
  3. Key Research and Development Program of Shaanxi Province [2021SF-103]

Ask authors/readers for more resources

This paper critically reviews metabolic pathways related to alcohol biosynthesis in C1-gas-utilizing microorganisms (CGUM) and summarizes metabolic engineering approaches used to enhance carbon conversion efficiency, microbial growth, and biosynthesis of desired alcohols. Challenges in efficient microbial conversion of C1 gaseous substrates are also explored and discussed. The strategies presented here could guide the development of efficient biological routes for CH4, CO2, and CO utilization.
C1 gaseous substrates (CH4, CO2, and CO) derived from natural gas, biogas, and syngas, are of interest due to their threats to the environment or inefficient utilization. Benefiting from advanced genetic editing tools and bioconversion strategies, metabolically engineered C1-gas-utilizing microorganisms (CGUM), such as methanotrophs, cyanobacteria, and acetogens, are capable of utilizing C1 gaseous feedstocks as the sole substrates for cell growth and synthesis of chemicals and biofuels. In this paper, we critically review metabolic pathways related to the assimilation of C1 gaseous substrates for alcohol biosynthesis in several model CGUM. Metabolic engineering approaches utilized to enhance the carbon conversion efficiency, microbial growth and biosynthesis of desired alcohols are summarized, including the regulation of C1 gaseous substrates activation and electron and energy supply, the accumulation of key intermediates, and the manipulation of target gene expression to optimize carbon flux to bioalcohols. In addition, challenges in the efficient microbial conversion of C1 gaseous substrates are explored and discussed. The strategies of bioalcohol biosynthesis presented here could guide the development of a variety of efficient biological routes for CH4, CO2, and CO utilization in the future.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available