Physiological and transcriptomic responses of Synechococcus sp. FACHB-805 to phosphite under phosphate limitation

IF 5 2区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Ye Zheng, Xingyao Ye, Xiaojun Niu, Dongqing Zhang, Mo Wang, Yang Yu, Ling Li, Chen Wang, Xiufang Yang, Xintai Su
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Abstract

With the increasing detection of phosphite (Phi) in aquatic systems, growing concern has emerged regarding its bioavailability and potential consequences for microbial nutrient utilization and carbon cycling. However, whether Phi can functionally substitute for phosphate (Pi), and how Phi exposure modifies cellular physiology and stress responses under Pi-deficient conditions, remain insufficiently understood in freshwater cyanobacteria. Here we systematically investigated the physiological, biochemical, ultrastructural, and transcriptional responses of the freshwater cyanobacterium Synechococcus sp. FACHB-805 to a Phi exposure gradient under contrasting Pi regimes. The results showed that Synechococcus sp. FACHB-805 lacks the functional ptxD-mediated enzymatic machinery required to oxidize phosphite into metabolically usable orthophosphate. This genetic deficiency fundamentally underpins the strain's inability to sustain population growth, chlorophyll-a accumulation, and Rubisco activity under phosphite-sole conditions. Elevated Phi exposure under Pi-limitation did not relieve the Pi-starvation state and was associated with higher malondialdehyde content and superoxide dismutase activity, together with transcriptional signatures suggestive of redox-stress-related adjustment and genome-maintenance-related responses. Together, these results indicate that Phi, even when unable to support growth as a sole phosphorus source, can shape the oxidative state, carbon fixation efficiency, and dissolved organic carbon release of dominant freshwater cyanobacteria under Pi limitation, underscoring the importance of incorporating phosphorus redox chemistry into assessments of microbial carbon cycling in P-limited aquatic ecosystems.
在磷酸盐限制下,聚球菌对亚磷酸盐的生理和转录组反应
随着亚磷酸盐(Phi)在水生系统中的检测越来越多,人们越来越关注其生物利用度及其对微生物养分利用和碳循环的潜在影响。然而,在淡水蓝藻中,Phi是否可以在功能上替代磷酸盐(Pi),以及在Pi缺乏的条件下,Phi暴露如何改变细胞生理和应激反应,仍未得到充分的了解。在这里,我们系统地研究了淡水蓝藻聚藻球菌sp. FACHB-805在不同的Pi制度下对Phi暴露梯度的生理、生化、超微结构和转录反应。结果表明,聚球菌(Synechococcus sp. FACHB-805)缺乏功能性ptxd介导的酶机制,无法将亚磷酸酯氧化为可代谢的正磷酸盐。这种遗传缺陷从根本上支持了该菌株在亚磷酸盐条件下无法维持种群增长、叶绿素-a积累和Rubisco活性。在pi限制下增加Phi暴露并不能缓解pi饥饿状态,并且与更高的丙二醛含量和超氧化物歧化酶活性以及提示氧化还原应激相关调节和基因组维持相关反应的转录特征相关。总之,这些结果表明,即使Phi不能作为唯一的磷源支持生长,也可以在Pi限制下塑造优势淡水蓝藻的氧化状态、固碳效率和溶解有机碳释放,强调将磷氧化还原化学纳入p限制水生生态系统中微生物碳循环评估的重要性。
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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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