生理、转录组学和代谢组学分析揭示了凝胶Betaphycus gelatinus在不同盐度条件下的适应机制

IF 4.5 2区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Algal Research-Biomass Biofuels and Bioproducts Pub Date : 2025-03-01 Epub Date: 2025-01-04 DOI:10.1016/j.algal.2025.103894
Hui Tian , Yongqiu Deng , Kangtai Liao , Siqi Xu , Jihong Chen , Linwen He
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引用次数: 0

摘要

明胶Betaphycus gelatinus是工业提取卡拉胶的重要原料,其生长和繁殖受盐度变化的影响较大。为了研究明胶小蠊在不同盐度条件下的适应机制,我们在15、20、25、30、35、40和45 psu条件下培养了7 d,并进行了生理、转录组学和代谢组学分析。盐胁迫显著降低了明胶鱼的生长速率、光合性能和色素含量,而超氧化物歧化酶(SOD)和抗坏血酸过氧化物酶(APX)活性以及丙二醛、可溶性糖和谷胱甘肽(GSH)含量显著升高。转录组学和代谢组学分析表明,光合作用、抗氧化系统、氮代谢、碳水化合物代谢、脂质合成和ABC转运蛋白可能参与了明胶芽孢杆菌的盐胁迫响应。在低盐度胁迫下,与光合作用、Calvin循环、抗坏血酸(AsA) - GSH循环、糖酵解/糖异生和戊糖磷酸途径相关的差异表达基因(DEGs)下调,而与氮代谢相关的差异表达基因(DEGs)上调。相反,在高盐胁迫下,与光合作用、叶绿素降解、卡尔文循环、AsA - GSH循环、脂质合成和ABC转运体相关的DEGs上调,而与叶绿素合成和氮代谢相关的DEGs下调。氨基酸含量在低盐胁迫下升高,在高盐胁迫下降低,饱和脂肪酸和不饱和脂肪酸含量在低盐和高盐胁迫下均升高。这些发现有助于阐明明胶双歧杆菌在不同盐度条件下的适应机制,为明胶双歧杆菌的高效工业化养殖提供理论指导。
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Physiological, transcriptomic, and metabolomic analyses reveal the adaptation mechanism of Betaphycus gelatinus under different salinity conditions
Betaphycus gelatinus is an essential raw material for the industrial extraction of carrageenan, and its growth and reproduction are significantly influenced by changes in salinity. To investigate the adaptation mechanisms of B. gelatinus under different salinity conditions, B. gelatinus was cultured for 7 d under 15, 20, 25, 30, 35, 40, and 45 psu and subjected to physiological, transcriptomic, and metabolomic analyses. The growth rate, photosynthetic performance and pigment content of B. gelatinus decreased significantly, while the activities of superoxide dismutase (SOD) and ascorbate peroxidase (APX) and contents of malondialdehyde, soluble sugar, and glutathione (GSH) increased significantly under salt stress. Transcriptomic and metabolomic analyses indicated that photosynthesis, antioxidant systems, nitrogen metabolism, carbohydrate metabolism, lipid synthesis, and ABC transporters may be involved in the salt stress response of B. gelatinus. Under low-salinity stress, differentially expressed genes (DEGs) associated with photosynthesis, Calvin cycle, ascorbate (AsA) − GSH cycle, glycolysis/gluconeogenesis, and the pentose phosphate pathway were downregulated, while those associated with nitrogen metabolism were upregulated. In contrast, under high-salinity stress, DEGs associated with photosynthesis, chlorophyll degradation, Calvin cycle, AsA − GSH cycle, lipid synthesis, and ABC transporters were upregulated, while those associated with chlorophyll synthesis and nitrogen metabolism were downregulated. The amino acid content was increased under low-salinity stress but decreased under high-salinity stress, while the contents of saturated fatty acids and unsaturated fatty acids were increased under both low and high salinity conditions. These findings help elucidate the adaptation mechanisms of B. gelatinus under varying salinity conditions and provide theoretical guidance for efficient industrial breeding of B. gelatinus.
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来源期刊
Algal Research-Biomass Biofuels and Bioproducts
Algal Research-Biomass Biofuels and Bioproducts BIOTECHNOLOGY & APPLIED MICROBIOLOGY-
CiteScore
9.40
自引率
7.80%
发文量
332
期刊介绍: Algal Research is an international phycology journal covering all areas of emerging technologies in algae biology, biomass production, cultivation, harvesting, extraction, bioproducts, biorefinery, engineering, and econometrics. Algae is defined to include cyanobacteria, microalgae, and protists and symbionts of interest in biotechnology. The journal publishes original research and reviews for the following scope: algal biology, including but not exclusive to: phylogeny, biodiversity, molecular traits, metabolic regulation, and genetic engineering, algal cultivation, e.g. phototrophic systems, heterotrophic systems, and mixotrophic systems, algal harvesting and extraction systems, biotechnology to convert algal biomass and components into biofuels and bioproducts, e.g., nutraceuticals, pharmaceuticals, animal feed, plastics, etc. algal products and their economic assessment
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