In vitro reconstitution of complexes of stress HliA protein with pigments

Q4 Environmental Science
BioRisk Pub Date : 2022-04-21 DOI:10.3897/biorisk.17.77306
L. Sharapova, N. Yurina
{"title":"In vitro reconstitution of complexes of stress HliA protein with pigments","authors":"L. Sharapova, N. Yurina","doi":"10.3897/biorisk.17.77306","DOIUrl":null,"url":null,"abstract":"Proteins similar to Hli (high light inducible) proteins of cyanobacteria are present in all photosynthetic eukaryotes and are necessary for survival in various stressful conditions, although their exact function is not fully understood. In current study, the recombinant stress-induced protein HliA of cyanobacterium Synechocystis was isolated and characterised for the first time. The synthetic gene of HliA protein was created and cloned into plasmid for expression of recombinant protein with Hisx6-tag at the C-terminus in bacteria. Recombinant HliA protein of Synechocystis was isolated by metal-affinity chromatography. The HliA protein was reconstituted with chlorophyll a and carotenoids. Using circular dichroism spectroscopy, it was shown that chlorophyll a and carotenoids interact in vitro with the HliA protein. The binding of pigments to the HliA protein favours the protective function of this protein. Apparently, Hli proteins are involved in the coordinated delivery of pigments for the biogenesis of photosynthetic complexes, thereby reducing the risk of accumulation of phototoxic free chlorophyll molecules. Current results are important for understanding the processes of photoprotection in either cyanobacteria or algae and higher plants.","PeriodicalId":38674,"journal":{"name":"BioRisk","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-04-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BioRisk","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3897/biorisk.17.77306","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Environmental Science","Score":null,"Total":0}
引用次数: 0

Abstract

Proteins similar to Hli (high light inducible) proteins of cyanobacteria are present in all photosynthetic eukaryotes and are necessary for survival in various stressful conditions, although their exact function is not fully understood. In current study, the recombinant stress-induced protein HliA of cyanobacterium Synechocystis was isolated and characterised for the first time. The synthetic gene of HliA protein was created and cloned into plasmid for expression of recombinant protein with Hisx6-tag at the C-terminus in bacteria. Recombinant HliA protein of Synechocystis was isolated by metal-affinity chromatography. The HliA protein was reconstituted with chlorophyll a and carotenoids. Using circular dichroism spectroscopy, it was shown that chlorophyll a and carotenoids interact in vitro with the HliA protein. The binding of pigments to the HliA protein favours the protective function of this protein. Apparently, Hli proteins are involved in the coordinated delivery of pigments for the biogenesis of photosynthetic complexes, thereby reducing the risk of accumulation of phototoxic free chlorophyll molecules. Current results are important for understanding the processes of photoprotection in either cyanobacteria or algae and higher plants.
In应激HliA蛋白与色素复合物的体外重建
类似于蓝藻Hli(高光诱导型)蛋白的蛋白质存在于所有光合真核生物中,是在各种压力条件下生存所必需的,尽管它们的确切功能尚不完全清楚。在本研究中,首次分离并鉴定了聚囊蓝细菌的重组应激诱导蛋白HliA。构建了HliA蛋白的合成基因,并将其克隆到质粒中,用于在细菌中表达C末端带有Hisx6标签的重组蛋白。用金属亲和色谱法分离得到聚囊藻HliA重组蛋白。利用叶绿素a和类胡萝卜素对HliA蛋白进行重组。利用圆二色光谱法研究了叶绿素a和类胡萝卜素在体外和HliA蛋白的相互作用。色素与HliA蛋白的结合有利于该蛋白的保护功能。显然,Hli蛋白参与了色素的协调递送,用于光合复合物的生物发生,从而降低了无光毒性叶绿素分子积累的风险。目前的结果对于理解蓝藻、藻类和高等植物的光保护过程很重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
BioRisk
BioRisk Environmental Science-Environmental Science (miscellaneous)
CiteScore
1.40
自引率
0.00%
发文量
44
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信