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首页> 外文期刊>Annals of Botany >Temporal regulation of cell-wall pectin methylesterase and peroxidase isoforms in cadmium-treated flax hypocotyl.
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Temporal regulation of cell-wall pectin methylesterase and peroxidase isoforms in cadmium-treated flax hypocotyl.

机译:镉处理的亚麻下胚轴中细胞壁果胶甲基酯酶和过氧化物酶同工型的时间调控。

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In hypocotyls of flax (Linum usitatissimum) cadmium-induced reorientation of growth (i.e. an increase in expansion and a decrease in elongation) coincides with marked changes in the methylesterification and cross-linking of homogalacturonans within various cell-wall (CW) domains. The aim of the present study was to examine the involvement of pectin methylesterase (PME) and peroxidase (PER) in this cadmium-induced CW remodelling. METHODS: CW proteins were extracted from hypocotyls of 10- and 18-d-old flax that had been treated or not treated with 0p"5 mM Cd(NO). PME and PER expression within these extracts was detected by LC/MS, by isoelectric focusing and enzyme activity assays. Transcript expression by RT-PCR of known flax PME and PER genes was also measured in corresponding samples. KEY RESULTS: In cadmium-treated seedlings, PME activity increased as compared with controls, particularly at day 10. The increased activity of PME was accompanied by increased abundance of both a basic protein isoform (B2) and a particular transcript (Lupme5). In contrast, induction of PER activity by cadmium was highest at day 18. Among the four reported PER genes, Flxper1 and 3 increased in abundance in the presence of cadmium at day 18. CONCLUSIONS: The temporal regulation of Lupme and Flxper genes and of their respective enzyme activities fits the previously reported cadmium-induced structural changes of homogalacturonans within the CWs. After PME-catalysed de-esterification of homogalacturonans, their cross-linking would depend on the activity of PERs interacting with calcium-dimerized blocks and reinforce the cell cohesion during the cadmium-induced swelling.
机译:在亚麻(Linum usitatissimum)的下胚轴中,镉诱导的生长重新定向(即扩张的增加和伸长的减少)与各种细胞壁(CW)域内高半乳糖醛酸的甲基酯化和交联发生显着变化。本研究的目的是研究果胶甲基酯酶(PME)和过氧化物酶(PER)在这种镉诱导的CW重塑中的作用。方法:从已用或未用0p“ 5 mM Cd(NO)处理的10和18日龄亚麻的下胚轴中提取CW蛋白。通过LC / MS,LC / MS检测这些提取物中的PME和PER表达。主要结果:在镉处理的幼苗中,与对照相比,尤其是在第10天,镉处理的幼苗中PME的活性增加了。 PME活性的提高伴随着碱性蛋白同工型(B2)和特定转录本(Lupme5)的丰度增加,相比之下,镉对PER活性的诱导在第18天最高。在四个报告的PER基因中,Flxper1和在第18天,有镉存在时3的丰度增加。结论:Lupme和Flxper基因及其各自酶活性的时间调控符合先前报道的镉诱导的同型半乳糖醛酸的结构变化在CW中。在PME催化的同型半乳糖醛酸去酯化后,它们的交联将取决于与钙二聚体嵌段相互作用的PER的活性,并在镉诱导的溶胀过程中增强细胞内聚力。

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