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盐胁迫下鱼腥藻7120中产生海藻糖的酶MTSase和MTHase

Trehalose-producing enzymes MTSase and MTHase in Anabaena 7120 under NaCl stress.

作者信息

Asthana Ravi K, Nigam Subhasha, Maurya Archana, Kayastha Arvind M, Singh Sureshwar P

机构信息

Centre of Advanced Study in Botany, Banaras Hindu University, Varanasi, 221005, India.

出版信息

Curr Microbiol. 2008 May;56(5):429-35. doi: 10.1007/s00284-008-9121-0. Epub 2008 Mar 6.

Abstract

Salt tolerance, a multigenic trait, necessitates knowledge about biosynthesis and function of candidate gene(s) at the cellular level. Among the osmolytes, trehalose biosynthesis in cyanobacteria facing NaCl stress is little understood. Anabaena 7120 filaments exposed to 150 mM: NaCl fragmented and recovered on transfer to -NaCl medium with the increased heterocysts frequency (7%) over the control (4%). Cells failed to retain Na+ beyond a threshold [2.19 mM/cm3 (PCV)]. Whereas NaCl-stressed cells exhibited a marginal rise in K+ (1.1-fold) only at 30 h, for Na+ it was 130-fold at 48 h over cells in control. A time-course study (0-54 h) revealed reduction in intracellular Na+ beyond 48 h [0.80 mM/cm3 (PCV)] suggestive of ion efflux. The NaCl-stressed cells showed differential expression of maltooligosyltrehalose synthase (MTSase; EC 5.4.99.15) and maltooligosyltrehalose trehalohydrolase (MTHase; EC 3.2.1.141) depending on the time and the extent of intracellular Na+ buildup.

摘要

耐盐性是一种多基因性状,需要在细胞水平上了解候选基因的生物合成和功能。在渗透调节物质中,人们对面对氯化钠胁迫的蓝藻中海藻糖的生物合成了解甚少。鱼腥藻7120丝状体暴露于150 mM氯化钠中会断裂,转移到无氯化钠培养基上后恢复,异形胞频率(7%)高于对照(4%)。细胞无法在超过阈值[2.19 mM/cm³(细胞压积)]的情况下保留钠离子。虽然氯化钠胁迫的细胞仅在30小时时钾离子略有升高(1.1倍),但在48小时时,钠离子相对于对照细胞升高了130倍。一项时间进程研究(0 - 54小时)显示,48小时后细胞内钠离子减少[0.80 mM/cm³(细胞压积)],表明存在离子外流。氯化钠胁迫的细胞中麦芽寡糖基海藻糖合酶(MTSase;EC 5.4.99.15)和麦芽寡糖基海藻糖海藻糖水解酶(MTHase;EC 3.2.1.141)的表达存在差异,这取决于细胞内钠离子积累的时间和程度。

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