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首页> 外文期刊>BMC Plant Biology >The nitrilase PtNIT1 catabolizes herbivore-induced nitriles in Populus trichocarpa
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The nitrilase PtNIT1 catabolizes herbivore-induced nitriles in Populus trichocarpa

机译:腈水解酶PtNIT1分解毛果杨中的草食动物诱导的腈

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摘要

Nitrilases are nitrile-converting enzymes commonly found within the plant kingdom that play diverse roles in nitrile detoxification, nitrogen recycling, and phytohormone biosynthesis. Although nitrilases are present in all higher plants, little is known about their function in trees. Upon herbivory, poplars produce considerable amounts of toxic nitriles such as benzyl cyanide, 2-methylbutyronitrile, and 3-methylbutyronitrile. In addition, as byproduct of the ethylene biosynthetic pathway upregulated in many plant species after herbivory, toxic β-cyanoalanine may accumulate in damaged poplar leaves. In this work, we studied the nitrilase gene family in Populus trichocarpa and investigated the potential role of the nitrilase PtNIT1 in the catabolism of herbivore-induced nitriles. A BLAST analysis revealed three putative nitrilase genes (PtNIT1, PtNIT2, PtNIT3) in the genome of P. trichocarpa. While PtNIT1 was expressed in poplar leaves and showed increased transcript accumulation after leaf herbivory, PtNIT2 and PtNIT3 appeared not to be expressed in undamaged or herbivore-damaged leaves. Recombinant PtNIT1 produced in Escherichia coli accepted biogenic nitriles such as β-cyanoalanine, benzyl cyanide, and indole-3-acetonitrile as substrates in vitro and converted them into the corresponding acids. In addition to this nitrilase activity, PtNIT1 showed nitrile hydratase activity towards β-cyanoalanine, resulting in the formation of the amino acid asparagine. The kinetic parameters of PtNIT1 suggest that the enzyme utilizes β-cyanoalanine and benzyl cyanide as substrates in vivo. Indeed, β-cyanoalanine and benzyl cyanide were found to accumulate in herbivore-damaged poplar leaves. The upregulation of ethylene biosynthesis genes after leaf herbivory indicates that herbivore-induced β-cyanoalanine accumulation is likely caused by ethylene formation. Our data suggest a role for PtNIT1 in the catabolism of herbivore-induced β-cyanoalanine and benzyl cyanide in poplar leaves.
机译:腈水解酶是植物界中常见的腈转化酶,在腈解毒,氮循环和植物激素生物合成中发挥着不同的作用。尽管所有高等植物中都存在腈水解酶,但对其在树木中的功能知之甚少。在食草时,白杨会产生大量有毒腈,例如氰化苄,2-甲基丁腈和3-甲基丁腈。此外,草食后许多植物物种中乙烯生物合成途径的副产物上调,有毒的β-氰丙氨酸可能积聚在受损的杨树叶片中。在这项工作中,我们研究了毛果杨(Populus trichocarpa)中的腈水解酶基因家族,并研究了腈水解酶PtNIT1在草食动物诱导的腈分解代谢中的潜在作用。 BLAST分析揭示了毛果番荔枝基因组中的三个假定的腈水解酶基因(PtNIT1,PtNIT2,PtNIT3)。虽然PtNIT1在白杨叶片中表达并显示出在叶片食草后增加的转录积累,但PtNIT2和PtNIT3似乎在未受损或食草动物受损的叶片中不表达。在大肠杆菌中产生的重组PtNIT1接受了生物腈,例如β-氰基丙氨酸,苄基氰和吲哚-3-乙腈作为底物,并将其转化为相应的酸。除了这种腈水解酶活性之外,PtNIT1还显示出针对β-氰基丙氨酸的腈水合酶活性,从而导致了氨基酸天冬酰胺的形成。 PtNIT1的动力学参数表明该酶在体内利用β-氰基丙氨酸和苄基氰化物作为底物。实际上,发现β-氰基丙氨酸和苄基氰化物在草食动物损坏的杨树叶片中积累。食草后乙烯生物合成基因的上调表明,食草动物诱导的β-氰基丙氨酸积累很可能是由乙烯形成引起的。我们的数据表明,PtNIT1在草食动物诱导的白杨叶片中的β-氰基丙氨酸和苄基氰的分解代谢中起作用。

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