Accompanied with the developments of gene editing and synthetic biology toolkits, various metabolic engineering strategies have been established for strain improvement to enhance the target metabolite production. Poly-γ-glutamic acid (γ-PGA) is a natural biopolymer that mainly produced by Bacillus, and low-level yield hinders its application. To address this problem, numerous approaches have been conducted to increase γ-PGA yield. In this review, we focus on the genetic and metabolic engineering of microorganism for γ-PGA production, including strengthening raw materials utilization and precursor supply, enhancing γ-PGA synthetase gene cluster, transcription regulation engineering, cofactor regeneration, energy engineering and blocking the synthetic pathways of by-products. Meanwhile, to attain the γ-PGA with different configurations (D/L) and molecular weights, the expression of γ-PGA synthetase, glutamate racemase and γ-PGA hydrolase were respectively manipulated. In addition, except for Bacillus, metabolic engineering of other hosts for high-level production of γ-PGA was also reviewed in this article. Finally, the prospect of metabolic engineering of γ-PGA production strain was discussed regarding the recent progress, challenge, and trends in this field.
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http://dx.doi.org/10.1007/s11274-022-03390-6 | DOI Listing |
J Orthop Surg Res
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Excellence Center for Hip & Knee Arthroplasty, Department of Orthopedic Surgery, Zuyderland Medical Center, Heerlen, The Netherlands.
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State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science, Guangdong Provincial Clinical Study Center for Ocular Diseases, Guangzhou, China.
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View Article and Find Full Text PDFJ Biol Chem
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CAS Key Laboratory of Quantitative Engineering Biology, Shenzhen Institute of Synthetic Biology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China. Electronic address:
Biomolecular condensates (BMCs) represent a group of organized and programmed systems that participate in gene transcription, chromosome organization, cell division, tumorigenesis, and aging. However, the understanding of BMCs in terms of internal organizations and external regulations remains at an early stage. Recently, novel approaches such as synthetic biology have been used for de novo synthesis of BMCs.
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