Hudek L, Premachandra D, Webster W A J, Bräu L
Centre for Regional and Rural Futures, Faculty of Science Engineering and Built Environment, Deakin University, Burwood, Victoria, Australia Centre for Cellular and Molecular Biology, School of Life and Environmental Sciences, Deakin University, Burwood, Victoria, Australia.
Centre for Regional and Rural Futures, Faculty of Science Engineering and Built Environment, Deakin University, Burwood, Victoria, Australia.
Appl Environ Microbiol. 2016 Oct 14;82(21):6344-6356. doi: 10.1128/AEM.01336-16. Print 2016 Nov 1.
In bacteria, limited phosphate availability promotes the synthesis of active uptake systems, such as the Pst phosphate transport system. To understand the mechanisms that facilitate phosphate accumulation in the cyanobacterium Nostoc punctiforme, phosphate transport systems were identified, revealing a redundancy of Pst phosphate uptake systems that exists across three distinct operons. Four separate PstB system components were identified. pstB1 was determined to be a suitable target for creating phenotypic mutations that could result in the accumulation of excessive levels of phosphate through its overexpression or in a reduction of the capacity to accumulate phosphate through its deletion. Using quantitative real-time PCR (qPCR), it was determined that pstB1 mRNA levels increased significantly over 64 h in cells cultured in 0 mM added phosphate and decreased significantly in cells exposed to high (12.8 mM) phosphate concentrations compared to the level in cells cultured under normal (0.8 mM) conditions. Possible compensation for the loss of PstB1 was observed when pstB2, pstB3, and pstB4 mRNA levels increased, particularly in cells starved of phosphate. The overexpression of pstB1 increased phosphate uptake by N. punctiforme and was shown to functionally complement the loss of PstB in E. coli PstB knockout (PstB) mutants. The knockout of pstB1 in N. punctiforme did not have a significant effect on cellular phosphate accumulation or growth for the most part, which is attributed to the compensation for the loss of PstB1 by alterations in the pstB2, pstB3, and pstB4 mRNA levels. This study provides novel in vivo evidence that PstB1 plays a functional role in phosphate uptake in N. punctiforme IMPORTANCE: Cyanobacteria have been evolving over 3.5 billion years and have become highly adept at growing under limiting nutrient levels. Phosphate is crucial for the survival and prosperity of all organisms. In bacteria, limited phosphate availability promotes the synthesis of active uptake systems. The Pst phosphate transport system is one such system, responsible for the internalization of phosphate when cells are in phosphate-limited environments. Our investigations reveal the presence of multiple Pst phosphate uptake systems that exist across three distinct operons in Nostoc punctiforme and functionally characterize the role of the gene product PstB1 as being crucial for the maintenance of phosphate accumulation. We demonstrate that the genes pstB2, pstB3, and pstB4 show alterations in expression to compensate for the deletion of pstB1 The overall outcomes of this work provide insights as to the complex transport mechanisms that exist in cyanobacteria like N. punctiforme, allowing them to thrive in low-phosphate environments.
在细菌中,磷酸盐供应有限会促进活性摄取系统的合成,例如Pst磷酸盐转运系统。为了了解促进点状念珠藻中磷酸盐积累的机制,对磷酸盐转运系统进行了鉴定,结果显示在三个不同的操纵子中存在Pst磷酸盐摄取系统的冗余。鉴定出了四个独立的PstB系统组件。确定pstB1是产生表型突变的合适靶点,通过其过表达可能导致磷酸盐过量积累,或者通过其缺失导致磷酸盐积累能力降低。使用定量实时PCR(qPCR)测定,在添加0 mM磷酸盐培养的细胞中,pstB1 mRNA水平在64小时内显著增加,而与在正常(0.8 mM)条件下培养的细胞水平相比,暴露于高(12.8 mM)磷酸盐浓度的细胞中pstB1 mRNA水平显著降低。当pstB2、pstB3和pstB4 mRNA水平增加时,尤其是在缺乏磷酸盐的细胞中,观察到了对PstB1缺失的可能补偿。pstB1的过表达增加了点状念珠藻对磷酸盐的摄取,并显示在功能上补充了大肠杆菌PstB基因敲除(PstB)突变体中PstB的缺失。在点状念珠藻中敲除pstB1在很大程度上对细胞磷酸盐积累或生长没有显著影响,这归因于pstB2、pstB3和pstB4 mRNA水平的改变对PstB1缺失的补偿。本研究提供了新的体内证据,表明PstB1在点状念珠藻的磷酸盐摄取中发挥功能作用。重要性:蓝细菌已经进化了35亿多年,并且已经非常擅长在营养物质有限的条件下生长。磷酸盐对所有生物的生存和繁荣至关重要。在细菌中,有限的磷酸盐供应促进活性摄取系统的合成。Pst磷酸盐转运系统就是这样一种系统,负责在细胞处于磷酸盐限制环境时将磷酸盐内化。我们的研究揭示了在点状念珠藻的三个不同操纵子中存在多个Pst磷酸盐摄取系统,并从功能上表征了基因产物PstB1对维持磷酸盐积累至关重要的作用。我们证明pstB2、pstB3和pstB4基因的表达发生改变以补偿pstB1的缺失。这项工作的总体结果为点状念珠藻等蓝细菌中存在的复杂转运机制提供了见解,使它们能够在低磷酸盐环境中茁壮成长。