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伤口诱导的质外体过氧化物酶活性:它们在活性氧生成和解毒中的作用

Wound-induced apoplastic peroxidase activities: their roles in the production and detoxification of reactive oxygen species.

作者信息

Minibayeva F, Kolesnikov O, Chasov A, Beckett R P, Lüthje S, Vylegzhanina N, Buck F, Böttger M

机构信息

Kazan Institute of Biochemistry and Biophysics, Russian Academy of Sciences, Kazan 420111, Russia.

出版信息

Plant Cell Environ. 2009 May;32(5):497-508. doi: 10.1111/j.1365-3040.2009.01944.x. Epub 2009 Jan 22.

Abstract

Production of reactive oxygen species (ROS) is a widely reported response of plants to wounding. However, the nature of enzymes responsible for ROS production and metabolism in the apoplast is still an open question. We identified and characterized the proteins responsible for the wound-induced production and detoxification of ROS in the apoplast of wheat roots (Triticum aestivum L.). Compared to intact roots, excised roots and leachates derived from them produced twice the amount of superoxide (O2(-)). Wounding also induced extracellular peroxidase (ECPOX) activity mainly caused by the release of soluble peroxidases with molecular masses of 37, 40 and 136 kD. Peptide mass analysis by electrospray ionization-quadrupole time-of-flight-tandem mass spectrometry (ESI-QTOF-MS/MS) following lectin affinity chromatography of leachates showed the presence of peroxidases in unbound (37 kD) and bound (40 kD) fractions. High sensitivity of O2(-)-producing activity to peroxidase inhibitors and production of O2(-) by purified peroxidases in vitro provided evidence for the involvement of ECPOXs in O2(-) production in the apoplast. Our results present new insights into the rapid response of roots to wounding. An important component of this response is mediated by peroxidases that are released from the cell surface into the apoplast where they can display both oxidative and peroxidative activities.

摘要

活性氧(ROS)的产生是植物对伤口广泛报道的一种反应。然而,负责质外体中ROS产生和代谢的酶的性质仍然是一个悬而未决的问题。我们鉴定并表征了负责小麦根(Triticum aestivum L.)质外体中伤口诱导的ROS产生和解毒的蛋白质。与完整根相比,切除的根及其产生的渗滤液产生的超氧化物(O2(-))量是完整根的两倍。伤口还诱导了细胞外过氧化物酶(ECPOX)活性,这主要是由分子量为37、40和136 kD的可溶性过氧化物酶的释放引起的。对渗滤液进行凝集素亲和色谱后,通过电喷雾电离-四极杆飞行时间串联质谱(ESI-QTOF-MS/MS)进行肽质量分析,结果显示未结合(37 kD)和结合(40 kD)部分中均存在过氧化物酶。产生O2(-)的活性对过氧化物酶抑制剂高度敏感,并且纯化的过氧化物酶在体外产生O2(-),这为ECPOX参与质外体中O2(-)的产生提供了证据。我们的结果为根对伤口的快速反应提供了新的见解。这种反应的一个重要组成部分是由从细胞表面释放到质外体中的过氧化物酶介导的,在质外体中它们可以表现出氧化和过氧化物活性。

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