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分子克隆与鉴定菜豆中热诱导的 LcOPR1,编码对氧合酶的基因。

Molecular cloning and characterization of heat-responsive LcOPR1, a gene encoding oxophytodienoic acid reductase in lentil.

机构信息

Department of Biotechnology, Faculty of Agricultural Technology, Al-Balqa Applied University, Al-Salt 19117, Jordan.

Department of Botany and Plant Physiology, Faculty of Agrobiology, Food and Natural Resources, Czech University of Life Sciences Prague, Kamycka 129, 165 00 Prague, Czech Republic.

出版信息

Cell Mol Biol (Noisy-le-grand). 2024 Jul 28;70(7):1-7. doi: 10.14715/cmb/2024.70.7.1.

Abstract

Improving crop plants using biotechnological implications is a promising and modern approach compared to traditional methods. High-temperature exposure to the reproductive stage induces flower abortion and declines grain filling performance, leading to smaller grain production and low yield in lentil and other legumes. Thus, cloning effective candidate genes and their implication in temperature stress tolerance in lentil (Lens culinaris Medik.) using biotechnological tools is highly demandable. The 12-oxophytodienoic acid reductases (OPRs) are flavin mononucleotide-dependent oxidoreductases with vital roles in plants. They are members of the old yellow enzyme (OYE) family. These enzymes are involved in the octadecanoid pathway, which contributes to jasmonic acid biosynthesis and is essential in plant stress responses. Lentil is one of the vital legume crops affected by the temperature fluctuations caused by global warming. Therefore, in this study, the LcOPR1 gene was successfully cloned and isolated from lentils using RT-PCR to evaluate its functional responses in lentil under heat stress. The bioinformatics analysis revealed that the full-length cDNA of LcOPR1 was 1303 bp, containing an 1134 bp open reading frames (ORFs), encoding 377 amino acids with a predicted molecular weight of 41.63 and a theoretical isoelectric point of 5.61. Bioinformatics analyses revealed that the deduced LcOPR1 possesses considerable homology with other plant 12-oxophytodienoic acid reductases (OPRs). Phylogenetic tree analysis showed that LcOPR1 has an evolutionary relationship with other OPRs in different plant species of subgroup I, containing enzymes that are not required for jasmonic acid biosynthesis. The expression analysis of LcOPR1 indicated that this gene is upregulated in response to the heat-stress condition and during recovery in lentil. This study finding might be helpful to plant breeders and biotechnologists in LcOPR1 engineering and/or plant breeding programs in revealing the biological functions of LcOPR1 in lentils and the possibility of enhancing heat stress tolerance by overexpressing LcOPR1 in lentil and other legume plants under high temperature.

摘要

利用生物技术手段改良作物是一种有前途和现代化的方法,相较于传统方法而言。高温暴露于生殖阶段会导致花器官败育和灌浆性能下降,从而导致小粒生产和小扁豆及其他豆科作物的低产。因此,利用生物技术工具克隆有效的候选基因及其在小扁豆(Lens culinaris Medik.)对温度胁迫耐受性中的应用具有很高的需求。12-氧代-植物二烯酸还原酶(OPRs)是黄素单核苷酸依赖性氧化还原酶,在植物中具有重要作用。它们是老黄酶(OYE)家族的成员。这些酶参与十八碳烯酸途径,该途径有助于茉莉酸生物合成,是植物应激反应所必需的。小扁豆是受全球变暖引起的温度波动影响的重要豆科作物之一。因此,在这项研究中,使用 RT-PCR 从小扁豆中成功克隆和分离出 LcOPR1 基因,以评估其在热胁迫下小扁豆中的功能反应。生物信息学分析表明,LcOPR1 的全长 cDNA 为 1303 bp,包含 1134 bp 的开放阅读框(ORFs),编码 377 个氨基酸,预测分子量为 41.63,理论等电点为 5.61。生物信息学分析表明,推导的 LcOPR1 与其他植物 12-氧代-植物二烯酸还原酶(OPRs)具有相当大的同源性。系统进化树分析表明,LcOPR1 与不同植物物种亚组 I 中的其他 OPR 具有进化关系,其中包含不需要进行茉莉酸生物合成的酶。LcOPR1 的表达分析表明,该基因在小扁豆对热胁迫条件的响应以及在恢复过程中上调。这项研究结果可能有助于植物育种家和生物技术人员在 LcOPR1 工程和/或小扁豆和其他豆科植物在高温下过表达 LcOPR1 以提高耐热性的植物育种计划中揭示 LcOPR1 在小扁豆中的生物学功能和可能性。

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