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从绿藻雨生红球藻中克隆、表达和鉴定一种新型植物型隐花色素基因。

Cloning, expression, and characterization of a novel plant type cryptochrome gene from the green alga Haematococcus pluvialis.

机构信息

Institute of Molecular Agriculture and Bioenergy, Shanxi Agricultural University, Taigu, 030801, China.

Key Laboratory of Coastal Biology and Biological Resources Utilization, Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai, 264003, China.

出版信息

Protein Expr Purif. 2020 Aug;172:105633. doi: 10.1016/j.pep.2020.105633. Epub 2020 Apr 4.

Abstract

A full-length cDNA sequence of plant type CRY (designated Hae-P-CRY) was cloned from the green alga Haematococcus pluvialis. The cDNA sequence was 3608 base pairs (bp) in length, which contained a 2988-bp open reading frame encoding 995 amino acids with molecular mass of 107.7 kDa and isoelectric point of 6.19. Multiple alignment analysis revealed that the deduced amino acid sequence of Hae-P-CRY shared high identity of 47-66% with corresponding plant type CRYs from other eukaryotes. The catalytic motifs of plant type CRYs were detected in the amino acid sequence of Hae-P-CRY including the typical PHR and CTE domains. Phylogenetic analysis showed that the Hae-P-CRY was grouped together with other plant type CRYs from green algae and higher plants, which distinguished from other distinct groups. The transcriptional level of Hae-P-CRY was strongly decreased after 0-4 h under HL stress. In addition, the Hae-P-CRY gene was heterologously expressed in Escherichia coli BL21 (DE3) and successfully purified. The typical spectroscopic characteristics of plant type CRYs were present in Hae-P-CRY indicated that it may be an active enzyme, which provided valuable clue for further functional investigation in the green alga H. pluvialis. These results lay the foundation for further function and interaction protein identification involved in CRYs mediated signal pathway under HL stress in H. pluvialis.

摘要

从绿藻雨生红球藻中克隆到了植物型 CRY 的全长 cDNA 序列(命名为 Hae-P-CRY)。cDNA 序列长 3608 个碱基对(bp),包含一个 2988bp 的开放阅读框,编码 995 个氨基酸,分子量为 107.7kDa,等电点为 6.19。多重序列比对分析表明,Hae-P-CRY 的推导氨基酸序列与其他真核生物相应的植物型 CRYs 具有 47-66%的高度同源性。在 Hae-P-CRY 的氨基酸序列中检测到了植物型 CRYs 的催化基序,包括典型的 PHR 和 CTE 结构域。系统发育分析表明,Hae-P-CRY 与绿藻和高等植物的其他植物型 CRYs 聚在一起,与其他明显的群体区分开来。在 HL 应激下,Hae-P-CRY 的转录水平在 0-4 小时后强烈降低。此外,Hae-P-CRY 基因在大肠杆菌 BL21(DE3)中异源表达并成功纯化。Hae-P-CRY 中存在典型的植物型 CRYs 的光谱特征表明它可能是一种活性酶,这为进一步研究 HL 应激下绿藻雨生红球藻中 CRYs 介导的信号通路的功能提供了有价值的线索。这些结果为进一步鉴定 CRYs 介导的信号通路在 HL 应激下参与的功能和相互作用蛋白奠定了基础。

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