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克隆一些热休克蛋白基因,用于进一步研究暴露于非生物胁迫下的阿氏浮丝藻的转录情况。

Cloning of some heat shock proteins genes for further transcriptional study of Planktothrix agardhii exposed to abiotic stress.

作者信息

Tran Chi Thi Du, Bernard Cécile, Comte Katia

机构信息

Faculty of Biology, Hanoi University of Science, VNU-Hanoi, Hanoi, Vietnam.

出版信息

Folia Microbiol (Praha). 2015 Jul;60(4):317-23. doi: 10.1007/s12223-014-0372-9. Epub 2014 Dec 25.

Abstract

Planktothrix agardhii is one of the freshwater cyanobacteria that can produce the hepatotoxin microcystins (MC)-a real threat to human and animal health. Knowledge of the biological role of MC in producing organisms is highly desired to understand the driving force of MC production. Recently, emerging evidences have suggested that MC may have protective role in cells facing environmental stress. If this is true, one should expect differences in the cellular protective mechanisms between MC-containing and MC-deficient mutant strains. To test this hypothesis, it would be essential to investigate the consequences of the loss of MC in Planktothrix in the transcriptional responses of its heat shock proteins (Hsps) to abiotic stresses-an important component of cellular stress response. However, a crucial first step is prerequisite for the isolation of hsp genes here, as the genome of Planktothrix has not been fully published. Therefore, we have successfully isolated four hsp genes including clpC (hsp100), htpG (hsp90), groEL (hsp60), and groES (hsp10) from Planktothrix agardhii PCC 7805 using ramped annealing PCR (RAN-PCR) with consensus-degenerate hybrid oligonucleotide primers (CODEHOP) and annealing control primer (ACP) system. In addition, some putative regulatory sequences found in the upstream region of groESL operon of Planktothrix agardhii were also discussed.

摘要

阿氏浮丝藻是一种能产生肝毒素微囊藻毒素(MC)的淡水蓝藻,对人类和动物健康构成了真正的威胁。为了理解微囊藻毒素产生的驱动力,人们非常渴望了解其在产生生物中的生物学作用。最近,新出现的证据表明,微囊藻毒素在面临环境压力的细胞中可能具有保护作用。如果这是真的,那么人们应该预期含微囊藻毒素和不含微囊藻毒素的突变菌株在细胞保护机制上存在差异。为了验证这一假设,研究阿氏浮丝藻中微囊藻毒素缺失对其热休克蛋白(Hsps)对非生物胁迫的转录反应的影响至关重要,热休克蛋白是细胞应激反应的重要组成部分。然而,在这里分离hsp基因的关键第一步是先决条件,因为阿氏浮丝藻的基因组尚未完全公布。因此,我们使用带有共有简并杂交寡核苷酸引物(CODEHOP)和退火控制引物(ACP)系统的梯度退火PCR(RAN-PCR),成功地从阿氏浮丝藻PCC 7805中分离出了四个hsp基因,包括clpC(hsp100)、htpG(hsp90)、groEL(hsp60)和groES(hsp10)。此外,还讨论了在阿氏浮丝藻groESL操纵子上游区域发现的一些假定调控序列。

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