在高含氮培养基条件下合成聚羟基丁酸(PHB)的蓝光单胞菌工程技术

IF 6.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Metabolic engineering Pub Date : 2024-11-01 DOI:10.1016/j.ymben.2024.10.012
Zhongnan Zhang , Mingwei Shao , Ge Zhang , Simian Sun , Xueqing Yi , Zonghao Zhang , Hongtao He , Kang Wang , Qitiao Hu , Qiong Wu , Guo-Qiang Chen
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引用次数: 0

摘要

微生物生长与生物产品合成(包括细胞内聚酯聚羟丁酸(PHB))之间存在权衡。在氮限制条件下,更多的碳通量被导向 PHB 合成,同时生长受到抑制,总体碳利用率降低,这与糖酵解衍生的丙酮酸脱羧过程中的次优碳利用率类似。本研究重新配置了蓝光单胞菌的中心碳网络,从理论和实践上提高了 PHB 产量。研究发现,下调谷氨酰胺合成酶(GS)活性可同步改善氮无限制条件下的PHB积累和细胞生长,在含有丰富氮源的摇瓶中生长和在同样含有丰富氮源的7升生物反应器中进行分批进料培养时,PHB产量分别从葡萄糖(克/克)提高到理论产量的85%,PHB滴度从7.6克/升提高到12.9克/升,PHB滴度从51克/升提高到65克/升。结果表明,葡萄糖转化效率和微生物生长之间的代谢平衡更好,有利于经济地生产 PHB。
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Engineering Halomonas bluephagenesis for synthesis of polyhydroxybutyrate (PHB) in the presence of high nitrogen containing media
The trade-offs exist between microbial growth and bioproduct synthesis including intracellular polyester polyhydroxybutyrate (PHB). Under nitrogen limitation, more carbon flux is directed to PHB synthesis while growth is inhibited with diminishing overall carbon utilization, similar to the suboptimal carbon utilization during glycolysis-derived pyruvate decarboxylation. This study reconfigured the central carbon network of Halomonas bluephagenesis to improve PHB yield theoretically and practically. It was found that the downregulation of glutamine synthetase (GS) activity led to a synchronous improvement on PHB accumulation and cell growth under nitrogen non-limitation condition, increasing the PHB yield from glucose (g/g) to 85% of theoretical yield, PHB titer from 7.6 g/L to 12.9 g/L, and from 51 g/L to 65 g/L when grown in shake flasks containing a rich N-source, and grown in a fed-batch cultivation conducted in a 7-L bioreactor also containing a rich N-source, respectively. Results offer better metabolic balance between glucose conversion efficiency and microbial growth for economic PHB production.
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来源期刊
Metabolic engineering
Metabolic engineering 工程技术-生物工程与应用微生物
CiteScore
15.60
自引率
6.00%
发文量
140
审稿时长
44 days
期刊介绍: Metabolic Engineering (MBE) is a journal that focuses on publishing original research papers on the directed modulation of metabolic pathways for metabolite overproduction or the enhancement of cellular properties. It welcomes papers that describe the engineering of native pathways and the synthesis of heterologous pathways to convert microorganisms into microbial cell factories. The journal covers experimental, computational, and modeling approaches for understanding metabolic pathways and manipulating them through genetic, media, or environmental means. Effective exploration of metabolic pathways necessitates the use of molecular biology and biochemistry methods, as well as engineering techniques for modeling and data analysis. MBE serves as a platform for interdisciplinary research in fields such as biochemistry, molecular biology, applied microbiology, cellular physiology, cellular nutrition in health and disease, and biochemical engineering. The journal publishes various types of papers, including original research papers and review papers. It is indexed and abstracted in databases such as Scopus, Embase, EMBiology, Current Contents - Life Sciences and Clinical Medicine, Science Citation Index, PubMed/Medline, CAS and Biotechnology Citation Index.
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