Soccio Mario, Marangi Marianna, Laus Maura N
Department of Agriculture, Food, Natural resources and Engineering, University of Foggia, Foggia, Italy.
Department of Clinic and Experimental Medicine, University of Foggia, Foggia, Italy.
Front Plant Sci. 2022 Jun 27;13:934523. doi: 10.3389/fpls.2022.934523. eCollection 2022.
Glyoxalase I (GLYI) catalyzes the rate-limiting step of the glyoxalase pathway that, in the presence of GSH, detoxifies the cytotoxic molecule methylglyoxal (MG) into the non-toxic D-lactate. In plants, MG levels rise under various abiotic stresses, so GLYI may play a crucial role in providing stress tolerance. In this study, a comprehensive genome database analysis was performed in durum wheat ( Desf.), identifying 27 candidate genes (). However, further analyses of phylogenetic relationships and conserved GLYI binding sites indicated that only nine genes encode for putative functionally active TdGLYI enzymes, whose distribution was predicted in three different subcellular compartments, namely cytoplasm, plastids and mitochondria. Expression profile by qRT-PCR analysis revealed that most of the putative active genes were up-regulated by salt and osmotic stress in roots and shoots from 4-day-old seedlings, although a different behavior was observed between the two types of stress and tissue. Accordingly, in the same tissues, hyperosmotic stress induced an increase (up to about 40%) of both GLYI activity and MG content as well as a decrease of GSH (up to about -60%) and an increase of GSSG content (up to about 7-fold) with a consequent strong decrease of the GSH/GSSG ratio (up to about -95%). Interestingly, in this study, we reported the first demonstration of the existence of GLYI activity in highly purified mitochondrial fraction. In particular, GLYI activity was measured in mitochondria from durum wheat (DWM), showing hyperbolic kinetics with Km and Vmax values equal to 92 ± 0.2 μM and 0.519 ± 0.004 μmol min mg of proteins, respectively. DWM-GLYI resulted inhibited in a competitive manner by GSH (Ki = 6.5 ± 0.7 mM), activated by Zn and increased, up to about 35 and 55%, under salt and osmotic stress, respectively. In the whole, this study provides basis about the physiological significance of GLYI in durum wheat, by highlighting the role of this enzyme in the early response of seedlings to hyperosmotic stress. Finally, our results strongly suggest the existence of a complete mitochondrial GLYI pathway in durum wheat actively involved in MG detoxification under hyperosmotic stress.
乙二醛酶I(GLYI)催化乙二醛酶途径的限速步骤,在谷胱甘肽(GSH)存在的情况下,将细胞毒性分子甲基乙二醛(MG)解毒为无毒的D-乳酸。在植物中,MG水平在各种非生物胁迫下会升高,因此GLYI可能在提供胁迫耐受性方面发挥关键作用。在本研究中,对硬粒小麦(Desf.)进行了全面的基因组数据库分析,鉴定出27个候选基因()。然而,对系统发育关系和保守的GLYI结合位点的进一步分析表明,只有9个基因编码推定具有功能活性的TdGLYI酶,其分布预测在三个不同的亚细胞区室,即细胞质、质体和线粒体中。通过qRT-PCR分析的表达谱显示,大多数推定的活性基因在4日龄幼苗的根和芽中受到盐和渗透胁迫的上调,尽管在两种胁迫和组织之间观察到不同的行为。相应地,在相同组织中,高渗胁迫诱导GLYI活性和MG含量增加(高达约40%),同时GSH含量降低(高达约-60%),GSSG含量增加(高达约7倍),从而导致GSH/GSSG比值大幅下降(高达约-95%)。有趣的是,在本研究中,我们首次证明了在高度纯化的线粒体组分中存在GLYI活性。具体而言,在硬粒小麦线粒体(DWM)中测量了GLYI活性,显示出双曲线动力学,其Km和Vmax值分别等于92±0.2μM和0.519±0.004μmol min mg蛋白质。DWM-GLYI被GSH以竞争性方式抑制(Ki = 6.5±0.7 mM),被Zn激活,并在盐胁迫和渗透胁迫下分别增加高达约35%和55%。总体而言,本研究通过强调该酶在幼苗对高渗胁迫的早期反应中的作用,为GLYI在硬粒小麦中的生理意义提供了依据。最后,我们的结果强烈表明硬粒小麦中存在完整的线粒体GLYI途径,在高渗胁迫下积极参与MG解毒。