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木霉属内切几丁质酶基因的表达提高了转基因甘蔗对赤腐病的抗性。

Expression of Trichoderma spp. endochitinase gene improves red rot disease resistance in transgenic sugarcane.

作者信息

Sharma Amandeep Sahil, Kalia Anu, Sharma Anuradha, Sidhu Mehar Singh, Sanghera Gulzar Singh, Chhabra Gautam, Sharma Manveer, Singh Manjinder, Patel Ekta, Das Piyali, Hazra Somak, Kaur Ajinder, Singla Deepak, Sandhu Jagdeep Singh

机构信息

School of Agricultural Biotechnology, Punjab Agricultural University, Ludhiana, India.

Electron Microscopy and Nanoscience Laboratory, Punjab Agricultural University, Ludhiana, India.

出版信息

PLoS One. 2024 Sep 16;19(9):e0310306. doi: 10.1371/journal.pone.0310306. eCollection 2024.

Abstract

Sugarcane (Saccharum spp.)is an economically useful crop grown globally for sugar, ethanol and biofuel production. The crop is vulnerable to fungus Colletotrichum falcatum known to cause red rot disease. The pathogen hydrolyses stalk parenchyma cells where sucrose is accumulated resulting in upto 75% losses in sugar recovery. In this study, transgenic sugarcane having resistance against red rot was developed by introducing Trichoderma spp. endochitinase following Agrobacterium mediated transformation. The transgene introduction and expression in genetically modified plants were verified through qRT-PCR revealing upto 6-fold enhancement in endochitinase expression than non-transgenic plants. Hyperspectral Imaging of transgenic plants displayed altered leaf reflectance spectra and vegetative indices that were positively correlated with ransgene expression. The bioassay with virulent pathotypes of C. falcatumCF08 and CF13 known for epiphytotic occurrence resulted in identification of resistant plant Chit 3-13.The plants with higher reflectance also displayed improved disease resistance, implying their early classification into resistant/susceptible. The losses in sucrose content were minimized (up to 4-fold) in inoculated resistant plant Chit 3-13 as compared to susceptible non-transgenic plant, and a fewer pathogen hyphae were detected in vascular cells of the former through optical microscopy. The electron micrographs confirmed sucrose-filled stalk parenchyma cells in Chit 3-13; in contrast, cells of non-transgenic inoculated plant were depleted of sucrose. The active sites involved in cleaving 1-4 β-glycoside bonds of N-acetyl-d-glucosaminein the pathogen hyphal walls were detected through endochitinase protein structural modelling. The transgenic sugarcane is an important source for in trogressingred rot resistance in plant breeding programs.

摘要

甘蔗(Saccharum spp.)是一种具有经济价值的作物,在全球范围内种植用于生产糖、乙醇和生物燃料。这种作物易受引起赤腐病的真菌胶孢炭疽菌(Colletotrichum falcatum)侵害。该病原体水解积累蔗糖的茎薄壁细胞,导致糖分回收率损失高达75%。在本研究中,通过农杆菌介导的转化引入木霉属(Trichoderma spp.)内切几丁质酶,培育出了抗赤腐病的转基因甘蔗。通过qRT-PCR验证了转基因在转基因植物中的导入和表达,结果显示内切几丁质酶的表达比非转基因植物增强了6倍。转基因植物的高光谱成像显示叶片反射光谱和植被指数发生了变化,这些变化与转基因表达呈正相关。对已知会流行发生的胶孢炭疽菌CF08和CF13强致病型进行的生物测定,鉴定出了抗性植株Chit 3-13。反射率较高的植株也表现出更好的抗病性,这意味着它们可以早期被分类为抗性/易感型。与易感的非转基因植株相比,接种的抗性植株Chit 3-13中蔗糖含量的损失最小化(高达4倍),并且通过光学显微镜在前一种植株的维管束细胞中检测到的病原体菌丝较少。电子显微镜照片证实Chit 3-13中茎薄壁细胞充满蔗糖;相比之下,非转基因接种植株的细胞中蔗糖耗尽。通过内切几丁质酶蛋白质结构建模,检测到病原体菌丝壁中参与切割N-乙酰-d-葡萄糖胺1-4β-糖苷键的活性位点。转基因甘蔗是植物育种计划中增强赤腐病抗性的重要来源。

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