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Improvement of succinate production from methane by combining rational engineering and laboratory evolution in Methylomonas sp. DH-1

Authors :
Jae-Hwan Jo
Jeong-Ho Park
Byung Kwon Kim
Seon Jeong Kim
Chan Mi Park
Chang Keun Kang
Yong Jun Choi
Hyejin Kim
Eun Yeol Lee
Myounghoon Moon
Gwon Woo Park
Sangmin Lee
Soo Youn Lee
Jin-Suk Lee
Won-Heong Lee
Jeong-Il Kim
Min-Sik Kim
Source :
Microbial Cell Factories, Vol 23, Iss 1, Pp 1-20 (2024)
Publication Year :
2024
Publisher :
BMC, 2024.

Abstract

Abstract Recently, methane has been considered a next-generation carbon feedstock due to its abundance and it is main component of shale gas and biogas. Methylomonas sp. DH-1 has been evaluated as a promising industrial bio-catalyst candidate. Succinate is considered one of the top building block chemicals in the agricultural, food, and pharmaceutical industries. In this study, succinate production by Methylomonas sp. DH-1 was improved by combining adaptive laboratory evolution (ALE) technology with genetic engineering in the chromosome of Methylomonas sp. DH-1, such as deletion of bypass pathway genes (succinate dehydrogenase and succinate semialdehyde dehydrogenase) or overexpression of genes related with succinate production (citrate synthase, pyruvate carboxylase and phosphoenolpyruvate carboxylase). Through ALE, the maximum consumption rate of substrate gases (methane and oxygen) and the duration maintaining high substrate gas consumption rates was enhanced compared to those of the parental strain. Based on the improved methane consumption, cell growth (OD600) increased more than twice, and the succinate titer increased by ~ 48% from 218 to 323 mg/L. To prevent unwanted succinate consumption, the succinate semialdehyde dehydrogenase gene was deleted from the genome. The first enzyme of TCA cycle (citrate synthase) was overexpressed. Pyruvate carboxylase and phosphoenolpyruvate carboxylase, which produce oxaloacetate, a substrate for citrate synthase, were also overproduced by a newly identified strong promoter. The new strong promoter was screened from RNA sequencing data. When these modifications were combined in one strain, the maximum titer (702 mg/L) was successfully improved by more than three times. This study demonstrates that successful enhancement of succinic acid production can be achieved in methanotrophs through additional genetic engineering following adaptive laboratory evolution.

Details

Language :
English
ISSN :
14752859
Volume :
23
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Microbial Cell Factories
Publication Type :
Academic Journal
Accession number :
edsdoj.3e82c576bdc3424aa99429f18112473f
Document Type :
article
Full Text :
https://doi.org/10.1186/s12934-024-02557-0