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dc.contributor.authorPyankov, V. I.en
dc.contributor.authorBlack Jr., C. C.en
dc.contributor.authorArtyusheva, E. G.en
dc.contributor.authorVoznesenskaya, E. V.en
dc.contributor.authorKu, M. S. B.en
dc.contributor.authorEdwards, G. E.en
dc.date.accessioned2022-05-12T08:13:02Z-
dc.date.available2022-05-12T08:13:02Z-
dc.date.issued1999-
dc.identifier.citationFeatures of Photosynthesis in Haloxylon Species of Chenopodiaceae that are Dominant Plants in Central Asian deserts / V. I. Pyankov, C. C. Black Jr., E. G. Artyusheva et al. // Plant and Cell Physiology. — 1999. — Vol. 40. — Iss. 2. — P. 125-134.en
dc.identifier.issn0032-0781-
dc.identifier.otherAll Open Access, Green3
dc.identifier.urihttp://elar.urfu.ru/handle/10995/111107-
dc.description.abstractHaloxylon aphyllum and H. persicum of Chenopodiaceae are dominant plants in the continental deserts of the Asian Irano-Turanian region. The photosynthetic organs, assimilating shoots and leaf-like cotyledons of these two species were studied to characterize their photosynthetic types. 13C/12C isotope ratios, the cellular anatomy of assimilating organs, primary photosynthetic products, and activities of carbon metabolism enzymes, RUBP carboxylase, PEP carboxylase, malic enzymes, and aspartate aminotransferase, indicate different pathways of CO~2 fixation in the photosynthetic organs. Assimilating shoots had attributes of the C4 photosynthesis entirely, while cotyledons lack Kranz-anatomy and incorporated CO2 via C3 photosynthesis. Cotyledons and seeds had lower δ13C values compared to shoots, consistent with the contribution of C3-like CO2 assimilation. Two pathways of carbon donation to the C3 cycle via decarboxylation of C4 acids in bundle sheath cells are suggested to occur in shoots of Haloxylon. The primary photosynthetic product malate can be utilized through NADP+-malic enzyme which occurs in high activity. NAD+-malic enzyme may contribute to C4 photosynthesis (some aspartate is formed as an initial product, the bundle sheath chloroplasts have some grana, and NAD+-malic enzyme is found in bundle sheath cells of shoots, all criteria for NAD+-malic enzyme type photosynthesis). We propose that organ diversity of CO2 fixation pathway in Haloxylon species is an important factor for their growth, survival and reproduction in continental climate deserts.en
dc.description.sponsorshipThe study was supported in part by a Civilian Research and Development Foundation Grant RB1-264 to V.P., E.A., E.V., G.E., and M.K., a NATO Collaborative Research Grant 970588 to C.C.B., and National Science Foundation Grant IBN 9317756 to G.E.E. V.I. Pyankov would like to thank CIES, Washington for a Fulbright Scholar Research Fellowship and the Department of Biochemistry and Molecular Biology, University of Georgia, Athens for provision of facilities during part of the work.en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherJapanese Society of Plant Physiologistsen1
dc.publisherOxford University Press (OUP)en
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.sourcePlant Cell Physiol.2
dc.sourcePlant and Cell Physiologyen
dc.subjectC3 PHOTOSYNTHESIS CA PHOTOSYNTHESISen
dc.subjectCARBON ISOTOPESen
dc.subjectCOTYLEDONSen
dc.subjectDESERTSen
dc.subjectHALOXYLONen
dc.subjectASIAen
dc.subjectASPARTATE AMINOTRANSFERASEen
dc.subjectCARBON DIOXIDEen
dc.subjectDECARBOXYLATIONen
dc.subjectDESERTen
dc.subjectENZYME ACTIVITYen
dc.subjectMALATE DEHYDROGENASE (DECARBOXYLATING)en
dc.subjectMALIC ACIDen
dc.subjectPHOSPHOENOLPYRUVATE CARBOXYLASEen
dc.subjectPHOTOSYNTHESISen
dc.subjectRIBULOSEBISPHOSPHATE CARBOXYLASEen
dc.subjectACER PENSYLVANICUMen
dc.subjectAMARANTHACEAEen
dc.subjectHALOXYLONen
dc.subjectHALOXYLON APHYLLUMen
dc.subjectHALOXYLON APHYLLUMen
dc.subjectHALOXYLON PERSICUMen
dc.subjectHALOXYLON PERSICUMen
dc.titleFeatures of Photosynthesis in Haloxylon Species of Chenopodiaceae that are Dominant Plants in Central Asian desertsen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.scopus0032971263-
local.contributor.employeePyankov, V.I., Department of Plant Physiology, Urals State University, Lenin Avenue 51, 620083 Ekaterinburg, Russian Federation; Black Jr., C.C., Dept. of Biochem. and Molec. Biology, University of Georgia, Athens, GA 30602, United States; Artyusheva, E.G., Department of Plant Physiology, Urals State University, Lenin Avenue 51, 620083 Ekaterinburg, Russian Federation; Voznesenskaya, E.V., Morphology and Anatomy Department, Komarov Botanical Institute RAS, Prof. Popov Street 2, 197376 St. Petersburg, Russian Federation; Ku, M.S.B., Botany Department, Washington State University, Pullman, WA 99164-4238, United States; Edwards, G.E., Botany Department, Washington State University, Pullman, WA 99164-4238, United Statesen
local.description.firstpage125-
local.description.lastpage134-
local.issue2-
local.volume40-
dc.identifier.wos000078719400001-
local.contributor.departmentDepartment of Plant Physiology, Urals State University, Lenin Avenue 51, 620083 Ekaterinburg, Russian Federation; Dept. of Biochem. and Molec. Biology, University of Georgia, Athens, GA 30602, United States; Morphology and Anatomy Department, Komarov Botanical Institute RAS, Prof. Popov Street 2, 197376 St. Petersburg, Russian Federation; Botany Department, Washington State University, Pullman, WA 99164-4238, United Statesen
local.identifier.pure53305572-
local.identifier.eid2-s2.0-0032971263-
local.identifier.wosWOS:000078719400001-
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