Malformation of mango inflorescences (MMI) disease causes severe economic losses worldwide. Present research investigates the underlying causes of MMI. Results revealed significantly higher levels of cyanide, a by-product of ethylene biosynthesis, in malformed inflorescences (MI) of mango cultivars. There was a significant rise in ACS transcripts, ACS enzyme activity and cyanide and ethylene levels in MI as compared to healthy inflorescences (HI). Significant differences in levels of methionine, phosphate, S-adenosyl-L-methionine, S-adenosyl-L-homocysteine, ascorbate and glutathione, and activities of dehydroascorbate reductase and glutathione reductase were seen in MI over HI. Further, a lower expression of β-cyanoalanine synthase (β-CAS) transcript was associated with decreased cellular β-CAS activity in MI, indicating accumulation of unmetabolized cyanide. TEM studies showed increased gum-resinosis and necrotic cell organelles, which might be attributed to unmetabolized cyanide. In field trials, increased malformed-necrotic-inflorescence (MNI) by spraying ethrel and decreased MNI by treating with ethylene inhibitors (silver and cobalt ions) further confirmed the involvement of cyanide in MMI. Implying a role for cyanide in MMI at the physiological and molecular level, this study will contribute to better understanding of the etiology of mango inflorescence malformation, and also help manipulate mango varieties genetically for resistance to malformation.

译文

芒果花序畸形 (MMI) 疾病在世界范围内造成严重的经济损失。本研究调查了MMI的根本原因。结果显示,芒果品种畸形花序 (MI) 中氰化物 (乙烯生物合成的副产品) 的含量明显更高。与健康的花序 (HI) 相比,MI中的ACS转录本,ACS酶活性以及氰化物和乙烯水平显着增加。在HI上的MI中,蛋氨酸,磷酸,S-腺苷-L-蛋氨酸,S-腺苷-L-高半胱氨酸,抗坏血酸和谷胱甘肽的水平以及脱氢抗坏血酸还原酶和谷胱甘肽还原酶的活性存在显着差异。此外,β-氰基丙氨酸合酶 (β-CAS) 转录物的较低表达与MI中细胞 β-CAS活性降低有关,表明未代谢的氰化物积累。TEM研究表明,牙龈树脂增生和坏死细胞器增加,这可能归因于未代谢的氰化物。在田间试验中,通过喷洒ethrel增加畸形坏死花序 (MNI),通过用乙烯抑制剂 (银和钴离子) 处理减少MNI,进一步证实了氰化物参与MMI。在生理和分子水平上暗示氰化物在MMI中的作用,这项研究将有助于更好地了解芒果花序畸形的病因,并有助于从基因上操纵芒果品种以抵抗畸形。

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