Functional characterization of lactate metabolism and its key regulatory genes reveals lactate-mediated modulation of carbon and nitrogen metabolism in Phaeodactylum tricornutum.

IF 4.9 2区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Jiawen Duan, Yi Zhang, Chenhui Li, Yimeng Zheng, Yanhua Zeng, Xin Zhang, Xiaoni Cai, Hao Long, Wei Ren, Zhenyu Xie, Aiyou Huang
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引用次数: 0

Abstract

Background: The marine diatom Phaeodactylum tricornutum plays a crucial role in global carbon and nitrogen cycling. Previous work revealed that lactate regulates carbon and nitrogen metabolism of P. tricornutum through protein lactylation, significantly affecting growth characteristics, photosynthetic efficiency, biochemical composition, and expression of genes related to carbon and nitrogen metabolism. However, the functional roles of lactate metabolism genes and their regulatory mechanisms in carbon-nitrogen homeostasis remain unexplored. This study aimed to characterize key lactate metabolism and regulatory genes (ldhA, Glo1, Glo2, D-LCR, GlxI, and GPCR) and elucidate their influence on carbon and nitrogen metabolic modulation in P. tricornutum.

Results: Overexpression (OE) and RNA silence (AS) of ldhA, Glo1, Glo2, D-LCR, GlxI, and GPCR revealed their roles in lactate metabolism and regulation. The overexpression of Glo2 and ldhA enhanced exogenous lactate utilization and total lipid accumulation under low nitrogen (LN) conditions. Additionally, the overexpression of Glo1 and D-LCR facilitated the utilization of exogenous lactate to cope with LN conditions. In contrast, the growth and L-lactate consumption rates of GlxI and GPCR overexpression strains were significantly lower than or not significantly different from those of the WT strain. The key enzyme involved in lactate metabolism, LDHA, was selected for further functional analysis. Western blot analysis suggested that ldhA overexpression promoted the lactylation of an approximately 40 kDa lactylated protein in P. tricornutum. 13C-labeling analysis demonstrated that ldhA overexpression in P. tricornutum accelerated lactate utilization and the processes of glycolysis, TCA cycle, CCM, and Calvin cycle. RNA-Seq analysis revealed that ldhA overexpression promoted cell division metabolism and lipid metabolism in P. tricornutum under LN conditions and glycerophospholipid metabolism under exogenous lactate addition conditions.

Conclusion: Lactate metabolism and lactylation metabolic processes mediated by LDHA, GLO1, GLO2 and D-LCR are important mechanisms by which lactate affects the growth of P. tricornutum, rapidly regulates carbon and nitrogen metabolism processes, and promotes the accumulation of lipids under LN conditions.

乳酸代谢及其关键调控基因的功能表征揭示了乳酸对三角褐指藻碳氮代谢的调节作用。
背景:海洋硅藻褐藻在全球碳氮循环中起着至关重要的作用。前期研究表明,乳酸通过蛋白质的乳酸化作用调节三角角藻的碳氮代谢,显著影响其生长特性、光合效率、生化组成以及碳氮代谢相关基因的表达。然而,乳酸代谢基因在碳氮稳态中的功能作用及其调控机制仍未被探索。本研究旨在对三角藻乳酸代谢及调控关键基因(ldhA、Glo1、Glo2、D-LCR、GlxI和GPCR)进行表征,并阐明其对三角藻碳氮代谢调控的影响。结果:ldhA、Glo1、Glo2、D-LCR、GlxI和GPCR的过表达(OE)和RNA沉默(AS)揭示了它们在乳酸代谢和调节中的作用。低氮(LN)条件下,Glo2和ldhA的过表达增强了外源乳酸利用和总脂质积累。此外,Glo1和D-LCR的过表达促进了外源性乳酸的利用,以应对LN条件。相比之下,GlxI和GPCR过表达菌株的生长速率和l -乳酸消耗速率均显著低于或无显著差异。参与乳酸代谢的关键酶LDHA被选中进行进一步的功能分析。Western blot分析表明,ldhA的过表达促进了三角草约40 kDa的乳酸化蛋白的乳酸化。13c标记分析表明,ldhA在三角草中的过表达加速了乳酸的利用和糖酵解、TCA循环、CCM和Calvin循环的过程。RNA-Seq分析显示,ldhA过表达促进了LN条件下三角棘豆的细胞分裂代谢和脂质代谢,以及外源乳酸添加条件下的甘油磷脂代谢。结论:LDHA、GLO1、GLO2和D-LCR介导的乳酸代谢和乳酸化代谢过程是LN条件下乳酸影响三角藻生长、快速调节碳氮代谢过程、促进脂质积累的重要机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Microbial Cell Factories
Microbial Cell Factories 工程技术-生物工程与应用微生物
CiteScore
9.30
自引率
4.70%
发文量
235
审稿时长
2.3 months
期刊介绍: Microbial Cell Factories is an open access peer-reviewed journal that covers any topic related to the development, use and investigation of microbial cells as producers of recombinant proteins and natural products, or as catalyzers of biological transformations of industrial interest. Microbial Cell Factories is the world leading, primary research journal fully focusing on Applied Microbiology. The journal is divided into the following editorial sections: -Metabolic engineering -Synthetic biology -Whole-cell biocatalysis -Microbial regulations -Recombinant protein production/bioprocessing -Production of natural compounds -Systems biology of cell factories -Microbial production processes -Cell-free systems
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