首页> 外文期刊>Journal of Experimental Botany >Pp6-FEH1 encodes an enzyme for degradation of highly polymerized levan and is transcriptionally induced by defoliation in timothy (Phleum pratense L.)
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Pp6-FEH1 encodes an enzyme for degradation of highly polymerized levan and is transcriptionally induced by defoliation in timothy (Phleum pratense L.)

机译:Pp6-FEH1编码用于降解高度聚合的levan的酶,并通过叶齿上的落叶(Phleum pratense L.)转录诱导。

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摘要

The ability of grasses to regrow after defoliation by cutting or grazing is a vital factor in their survival and an important trait when they are used as forage crops. In temperate grass species accumulating fructans, defoliation induces the activity of a fructan exohydrolase (FEH) that degrades fructans to serve as a carbon source for regrowth. Here, a cDNA from timothy was cloned, named Pp6-FEH1, that showed similarity to wheat fructan 6-exohydrolase (6-FEH). The recombinant enzyme expressed in Pichia pastoris completely degraded fructans that were composed mainly of β(2,6)-linked and linear fructans (levan) with a high degree of polymerization (DP) in the crown tissues of timothy. The substrate specificity of Pp6-FEH1 differed from previously characterized enzymes with 6-FEH activity in fructan-accumulating plants: (i) Pp6-FEH1 showed 6-FEH activity against levan (mean DP 20) that was 4-fold higher than against 6-kestotriose (DP 3), indicating that Pp6-FEH1 has a preference for β(2,6)-linked fructans with high DP; (ii) Pp6-FEH1 had significant activity against β(2,1)-linked fructans, but considerably less than against β(2,6)-linked fructans; (iii) Pp6-FEH1 had weak invertase activity, and its 6-FEH activity was inhibited slightly by sucrose. In the stubble of seedlings and in young haplocorms from adult timothy plants, transcripts of Pp6-FEH1 were significantly increased within 3 h of defoliation, followed by an increase in 6-FEH activity and in the degradation of fructans. These results suggest that Pp6-FEH1 plays a role in the degradation of fructans and the mobilization of carbon sources for regrowth after defoliation in timothy.
机译:割草或放牧后,草在脱叶后恢复生长的能力是其生存的重要因素,并且用作草料作物时的重要特性。在积聚果聚糖的温带草种中,脱叶诱导果聚糖外切水解酶(FEH)的活性,该酶降解果聚糖以充当再生长的碳源。在这里,从蒂莫西克隆了一个名为Pp6-FEH1的cDNA,该cDNA与小麦果聚糖6-外切水解酶(6-FEH)相似。在巴斯德毕赤酵母中表达的重组酶完全降解了果聚糖,在果皮的冠状组织中,果聚糖主要由具有高度聚合度(DP)的β(2,6)连接和线性果聚糖(levan)组成。 Pp6-FEH1的底物特异性不同于先前鉴定的在富集果聚糖的植物中具有6-FEH活性的酶:(i)Pp6-FEH1显示出对levan的6-FEH活性(平均DP 20)比对6的高4倍。 -酮三糖(DP 3),表明Pp6-FEH1优先选择具有高DP的β(2,6)-连接的果聚糖。 (ii)Pp6-FEH1对β(2,1)连接的果聚糖具有显着的活性,但远小于对β(2,6)连接的果聚糖的活性; (iii)Pp6-FEH1具有弱的转化酶活性,其6-FEH活性受到蔗糖的轻微抑制。在成年的提摩太植物的幼苗的残茬和年轻的单倍体中,Pp6-FEH1的转录本在脱叶后3小时内显着增加,随后6-FEH活性增加且果聚糖降解。这些结果表明,Pp6-FEH1在果胶脱叶后在果聚糖的降解和碳源的再生中发挥作用。

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