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首页> 外文期刊>Journal of Plant Physiology >Molecular cloning and characterization of cDNAs encoding cinnamoyl CoA reductase (CCR) from barley (Hordeum vulgare)(a) and potato (Solanum tuberosum)(a)
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Molecular cloning and characterization of cDNAs encoding cinnamoyl CoA reductase (CCR) from barley (Hordeum vulgare)(a) and potato (Solanum tuberosum)(a)

机译:大麦(Aordeum vulgare)(a)和马铃薯(Solanum tuberosum)(a)编码肉桂酰辅酶A还原酶(CCR)的cDNA的分子克隆和表征

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摘要

Cinnamoyl CoA reductase catalyzes the reduction of cinnamic acid CoA esters into their corresponding aldehydes, the first step of the phenylpropanoid pathway specifically dedicated to monolignol biosynthesis. Two cDNA clones encoding cinnamoyl CoA reductase (CCR) have been isolated from Hordeum vulgare (HvCCR) and Solanum tuberosum (StCCR1). Amino acid sequence alignment revealed the motif, NWYCY, representing the active site of CCR, conserved in both the encoded HvCCR and StCCR1 amino acid sequences. The HvCCR encoded protein possesses substantial homology with CCRs isolated and cloned form other sources; the highest identity (89%) was observed with CCR from fescue (Festuca arundicinea). Expression analysis by RT-PCR demonstrated that the HvCCR gene is expressed in barley stem and root tissue while no expression is detected in leaves and flowers. This expression pattern suggests that HvCCR is involved in constitutive lignification. Transcripts of StCCR1 were detected in potato root, leaf and also in stem although at a very low level.
机译:肉桂酰基CoA还原酶催化肉桂酸CoA酯还原成其相应的醛,这是专门用于单木酚生物合成的苯丙烷途径的第一步。从大麦(HvCCR)和马铃薯茄(StCCR1)中分离了两个编码肉桂酰基辅酶A还原酶(CCR)的cDNA克隆。氨基酸序列比对揭示了基序NWYCY,代表CCR的活性位点,在编码的HvCCR和StCCR1氨基酸序列中均保守。 HvCCR编码的蛋白质与从其他来源分离和克隆的CCR具有基本的同源性。羊茅(Festuca arundicinea)的CCR具有最高的同一性(89%)。通过RT-PCR的表达分析表明,HvCCR基因在大麦茎和根组织中表达,而在叶和花中未检测到表达。这种表达模式表明HvCCR参与组成性木质化。在马铃薯的根,叶和茎中均检测到StCCR1的转录本,尽管其水平非常低。

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