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Overexpression of alfalfa mitochondrial HSP23 in prokaryotic and eukaryotic model systems confers enhanced tolerance to salinity and arsenic stress

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dc.contributor.authorLee, Ki-Won-
dc.contributor.authorCha, Joon-Yung-
dc.contributor.authorKim, Kyung-Hee-
dc.contributor.authorKim, Yong-Goo-
dc.contributor.authorLee, Byung-Hyun-
dc.contributor.authorLee, Sang-Hoon-
dc.date.accessioned2022-12-27T02:01:53Z-
dc.date.available2022-12-27T02:01:53Z-
dc.date.issued2012-01-
dc.identifier.issn0141-5492-
dc.identifier.issn1573-6776-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/22408-
dc.description.abstractThe cloning and characterization of a gene (MsHSP23) coding for a heat shock protein in alfalfa in a prokaryotic and model plant system is described. MsHSP23 contains a 633 bp ORF encoding a polypeptide of 213 amino acids and exhibits greater sequence similarity to mitochondrial sHSPs from dicotyledons than to those from monocotyledons. When expressed in bacteria, recombinant MsHSP23 conferred tolerance to salinity and arsenic stress. Furthermore, MsHSP23 was cloned in a plant expressing vector and transformed into tobacco, a eukaryotic model organism. The transgenic plants exhibited enhanced tolerance to salinity and arsenic stress under ex vitro conditions. In comparison to wild type plants, the transgenic plants exhibited significantly lower electrolyte leakage. Moreover, the transgenic plants had superior germination rates when placed on medium containing arsenic. Taken together, these overexpression results imply that MsHSP23 plays an important role in salinity and arsenic stress tolerance in transgenic tobacco. This approach could be useful to develop stress tolerant crops including forage crops.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherSPRINGER-
dc.titleOverexpression of alfalfa mitochondrial HSP23 in prokaryotic and eukaryotic model systems confers enhanced tolerance to salinity and arsenic stress-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1007/s10529-011-0750-1-
dc.identifier.scopusid2-s2.0-83055192081-
dc.identifier.wosid000297862100023-
dc.identifier.bibliographicCitationBIOTECHNOLOGY LETTERS, v.34, no.1, pp 167 - 174-
dc.citation.titleBIOTECHNOLOGY LETTERS-
dc.citation.volume34-
dc.citation.number1-
dc.citation.startPage167-
dc.citation.endPage174-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.subject.keywordPlusHEAT-SHOCK PROTEINS-
dc.subject.keywordPlusHETEROLOGOUS EXPRESSION-
dc.subject.keywordPlusSUPEROXIDE-DISMUTASE-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusPHOTOSYSTEM-II-
dc.subject.keywordPlusACCUMULATION-
dc.subject.keywordPlusGENES-
dc.subject.keywordAuthorAbiotic stress-
dc.subject.keywordAuthorArsenic-
dc.subject.keywordAuthorE. coli-
dc.subject.keywordAuthorHeat shock proteins-
dc.subject.keywordAuthorMedicago sativa-
dc.subject.keywordAuthorMsHSP23-
dc.subject.keywordAuthorSalinity stress-
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