Synechocystis PCC6803 and PCC6906 dnaK2 expression confers salt and oxidative stress tolerance in Arabidopsis via reduction of hydrogen peroxide accumulation

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dc.contributor.authorJonghyun Kim-
dc.contributor.authorMyung-Suk Ahn-
dc.contributor.authorYoung Min Park-
dc.contributor.authorSuk Weon Kim-
dc.contributor.authorSung Ran Min-
dc.contributor.authorWon Joong Jeong-
dc.contributor.authorJang Ryol Liu-
dc.date.accessioned2017-04-19T09:52:58Z-
dc.date.available2017-04-19T09:52:58Z-
dc.date.issued2014-
dc.identifier.issn0301-4851-
dc.identifier.uri10.1007/s11033-013-2955-yko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/11972-
dc.description.abstractAbiotic stress slows plant growth and development. Because salt stress, particularly from NaCl, acts as an important limiting factor in agricultural productivity, the identification and manipulation of genes related to salt tolerance could improve crop productivity. Prokaryotic, heat shock protein (Hsp), DnaK from the ubiquitous Hsp70 family is upregulated in cells that are under abiotic stress. Synechocystis spp. cyanobacteria encode at least three potential DnaK proteins in their genome. Here, expressions of dnaK1s and dnaK2s from two Synechocystis spp. PCC6803 (Sy6803) and PCC6906 (Sy6906), enhanced salt tolerance in a dnaK-defective Escherichia coli strain. In contrast, dnaK3s in both strains were ineffective, indicating that dnaK3 is functionally different from dnaK1 and dnaK2 in Synechocystis spp. under salt stress. Ectopic expression of dnaK2s from Sy6803 and Sy6906 conferred salt tolerance in transgenic Arabidopsis plants, which exhibited greater root length, chlorophyll content, fresh weight, and survival rate than wild type plants, all in the presence of NaCl. In transgenic plants, hydrogen peroxide (H2O2) accumulation was reduced under NaCl stress and loss of chlorophyll content was reduced under H2O2 stress. Overall results suggest that dnaK2s from Sy6803 and Sy6906 confer salt and oxidative tolerance in transgenic plants by reduction of H2O2 accumulation.-
dc.publisherSpringer-
dc.titleSynechocystis PCC6803 and PCC6906 dnaK2 expression confers salt and oxidative stress tolerance in Arabidopsis via reduction of hydrogen peroxide accumulation-
dc.title.alternativeSynechocystis PCC6803 and PCC6906 dnaK2 expression confers salt and oxidative stress tolerance in Arabidopsis via reduction of hydrogen peroxide accumulation-
dc.typeArticle-
dc.citation.titleMolecular Biology Reports-
dc.citation.number2-
dc.citation.endPage1101-
dc.citation.startPage1091-
dc.citation.volume41-
dc.contributor.affiliatedAuthorJonghyun Kim-
dc.contributor.affiliatedAuthorMyung-Suk Ahn-
dc.contributor.affiliatedAuthorYoung Min Park-
dc.contributor.affiliatedAuthorSuk Weon Kim-
dc.contributor.affiliatedAuthorSung Ran Min-
dc.contributor.affiliatedAuthorWon Joong Jeong-
dc.contributor.affiliatedAuthorJang Ryol Liu-
dc.contributor.alternativeName김종현-
dc.contributor.alternativeName안명숙-
dc.contributor.alternativeName박영민-
dc.contributor.alternativeName김석원-
dc.contributor.alternativeName민성란-
dc.contributor.alternativeName정원중-
dc.contributor.alternativeName유장렬-
dc.identifier.bibliographicCitationMolecular Biology Reports, vol. 41, no. 2, pp. 1091-1101-
dc.identifier.doi10.1007/s11033-013-2955-y-
dc.subject.keywordArabidopsis thaliana-
dc.subject.keywordHydrogen peroxide-
dc.subject.keywordSalt stress tolerance-
dc.subject.keywordSynechocystis-
dc.subject.keywordTransgenic plants-
dc.subject.localArabidopsis thaliana-
dc.subject.localHydrogen peroxide-
dc.subject.localhydrogen peroxide-
dc.subject.localSalt stress tolerance-
dc.subject.localSynechocystis-
dc.subject.localTrans-genic plants-
dc.subject.localTransgenic Plant-
dc.subject.localTransgenic plant-
dc.subject.localTransgenic plants-
dc.subject.localtransgenic plant-
dc.description.journalClassY-
Appears in Collections:
Jeonbuk Branch Institute > Biological Resource Center > 1. Journal Articles
Division of Research on National Challenges > Plant Systems Engineering Research > 1. Journal Articles
Synthetic Biology and Bioengineering Research Institute > Cell Factory Research Center > 1. Journal Articles
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