Počet záznamů: 1  

Phosphoenolpyruvate carboxylase, NADP-malic enzyme, and pyruvate, phosphate dikinase are involved in the acclimation of Nicotiana tabacum L. to drought stress

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    0429982 - ÚEB 2015 RIV DE eng J - Článek v odborném periodiku
    Doubnerová-Hýsková, V. - Miedzińska, L. - Dobrá, Jana - Vaňková, Radomíra - Ryšlavá, H.
    Phosphoenolpyruvate carboxylase, NADP-malic enzyme, and pyruvate, phosphate dikinase are involved in the acclimation of Nicotiana tabacum L. to drought stress.
    Journal of Plant Physiology. Roč. 171, č. 5 (2014), s. 19-25. ISSN 0176-1617. E-ISSN 1618-1328
    Grant CEP: GA MŠMT 1M0505
    Institucionální podpora: RVO:61389030
    Klíčová slova: Drought * NADP-malic enzyme * Nicotiana tabacum L.
    Kód oboru RIV: EI - Biotechnologie a bionika
    Impakt faktor: 2.557, rok: 2014

    Drought stress is one of the most frequent forms of abiotic stresses, which occurs under condition of limited water availability. In this work, the possible participation of phosphoenolpyruvate carboxylase (EC 4.1.1.31; PEPC), NADP-malic enzyme (EC 1.1.1.40; NADP-ME), and pyruvate, phosphate dikinase (EC 2.7.9.1; PPDK) in response to drought of tobacco plants (Nicotiana tabacum L, cv. W38) was investigated. Enzyme specific activities in tobacco leaves of drought stressed plants were significantly increased after 11 days of stress, PEPC 2.3-fold, NADP-ME 3.9-fold, and PPDK 2.7-fold compared to control plants. The regulation of PEPC and NADP-ME activities were studied on transcriptional level by the quantitative RT PCR and on translational level - immunochemically. The amount of NADP-ME protein and transcription of mRNA for chloroplastic NADP-ME isoform were increased indicating their enhanced synthesis de novo. On the other hand, mRNA for cytosolic isoform of NADP-ME was decreased. The changes in PEPC protein and PEPC mRNA were not substantial. Therefore regulation of PEPC activity by phosphorylation was evaluated and found to be involved in the stress response. During recovery, activities of the tested enzymes returned close to their basal levels.
    Trvalý link: http://hdl.handle.net/11104/0234926

     
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