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Effects of exogenous spermidine on photosynthetic capacity and expression of Calvin cycle genes in salt-stressed cucumber seedlings

机译:外源亚精胺对盐胁迫黄瓜幼苗光合能力和Calvin循环基因表达的影响

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摘要

We investigated the effects of exogenous spermidine (Spd) on growth, photosynthesis and expression of the Calvin cycle-related genes in cucumber seedlings (Cucumis sativus L.) exposed to NaCl stress. Salt stress reduced net photosynthetic rates (P_N), actual photochemical efficiency of PSII (UPSII) and inhibited plant growth. Application of exogenous Spd to salinized nutrient solution alleviated salinity-induced the inhibition of plant growth, together with an increase in P_N and UPSII. Salinity markedly reduced the maximum carboxylase activity of ribulose-1,5-bisphosphate carboxylase/oxygenase (Vcmax), the maximal velocity of RuBP regeneration (Jmax), triosephosphate utilization capacity (TPU) and carboxylation efficiency (CE). Spd alleviated the negative effects on CO_2 assimilation induced by salt stress. Moreover, Spd significantly increased the activities and contents of ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) and fructose-1,6-biphosphate aldolase (ALD; aldolase) in the salt-stressed cucumber leaves. On the other hand, salinity up-regulated the transcriptional levels of ribulose-1,5-bisphosphate (RCA), glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and phosphoribrokinase (PRK) and down-regulated the transcriptional levels of ribulose-1,5-bisphosphate carboxylase/oxygenase large subunit (RbcL), ribulose-1,5-bisphosphate carboxylase/oxygenase small subunit (RbcS), ALD, triose-3-phosphate isomerase (TPI), fructose-1,6-bisphosphate phosphatase (FBPase) and 3-phosphoglyceric acid kinase (PGK). However, Spd application to salt-stressed plant roots counteracted salinity-induced mRNA expression changes in most of the above-mentioned genes. These results suggest that Spd could improve photosynthetic capacity through regulating gene expression and activity of key enzymes for CO_2 fixation, thus confers tolerance to salinity on cucumber plants.
机译:我们调查了外源亚精胺(Spd)对NaCl胁迫下黄瓜幼苗(Cucumis sativus L.)生长,光合作用和Calvin循环相关基因表达的影响。盐胁迫降低了净光合速率(P_N),PSII的实际光化学效率(UPSII)并抑制了植物的生长。外源Spd在盐碱化的营养液中的施用减轻了盐碱化对植物生长的抑制作用,同时增加了P_N和UPSII。盐度显着降低了核糖-1,5-双磷酸羧化酶/加氧酶的最大羧化酶活性(Vcmax),RuBP再生的最大速度(Jmax),磷酸三糖利用能力(TPU)和羧化效率(CE)。 Spd减轻了盐胁迫对CO_2同化的负面影响。此外,Spd显着提高了盐胁迫黄瓜叶片中核糖-1,5-双磷酸羧化酶/加氧酶(Rubisco)和果糖-1,6-双磷酸醛缩酶(ALD;醛缩酶)的活性和含量。另一方面,盐度上调了1,5-双磷酸核糖(RCA),3磷酸甘油醛脱氢酶(GAPDH)和磷酸溴激酶(PRK)的转录水平,并下调了1的核糖1, 5-二磷酸羧化酶/加氧酶大亚基(RbcL),1,5-双磷酸核糖羧化酶/加氧酶小亚基(RbcS),ALD,3-磷酸三糖异构酶(TPI),果糖1,6-6-双磷酸磷酸酶(FBPase) )和3-磷酸甘油酸激酶(PGK)。但是,Spd应用于盐胁迫的植物根部,抵消了大多数上述基因中盐度诱导的mRNA表达变化。这些结果表明,Spd可以通过调节基因表达和固定CO_2的关键酶的活性来提高光合能力,从而赋予黄瓜植物耐盐性的能力。

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