Hossain Md Firose, Billah Mutasim, Ali Md Roushan, Parvez Md Sorwer Alam, Zaoti Zannati Ferdous, Hasan S M Zia, Hasan Md Faruk, Dutta Amit Kumar, Khalekuzzaman Md, Islam Md Asadul, Sikdar Biswanath
Professor Joarder DNA & Chromosome Research Lab, Department of Genetic Engineering and Biotechnology, University of Rajshahi, Rajshahi 6205, Bangladesh.
Department of Genetic Engineering and Biotechnology, Shahjalal University of Science and Technology, Sylhet 3114, Bangladesh.
Saudi J Biol Sci. 2021 Dec;28(12):6972-6986. doi: 10.1016/j.sjbs.2021.07.069. Epub 2021 Aug 2.
is a harmful pathogen that causes severe wilt disease in several vegetables. In the present study, we identified from wilt of papaya by 16S rRNA PCR amplification. Virulence ability of was determined by amplification of approximately 1500 bp clear band of gene. Further, seed germination assay showed that reduced the germination rate up to 26.21%, 34% and 33.63% of cucumber, bottle guard and pumpkin seeds, respectively whereas shoot and root growth were also significantly decreased. Moreover, growth inhibition of was recorded using antibacterial compound from medicinal plant and antagonistic Petroleum ether root extract of showed highest 22 ± 0.04 mm diameter of zone of inhibition where methanolic extract of and ethanolic extract of exhibited 20 ± 0.06 mm and 20 ± 0.01 mm zone of inhibition against , respectively In addition, bioactive compounds of inhibited growth by generating 17 ± 0.09 mm zone of inhibition. To unveil the inhibition mechanism, we adopted chemical-protein interaction network and molecular docking approaches where we found that, rutin from interacts with citrate (Si)-synthase and dihydrolipoyl dehydrogenase of with binding affinity of -9.7 kcal/mol and -9.5 kcal/mol while quercetin from interacts with the essential protein F0F1 ATP synthase subunit alpha of the with binding affinity of -6.9 kcal/mol and inhibit the growth of . Our study will give shed light on the development of eco-friendly biological control of wilt disease of papaya.
是一种有害病原体,可在多种蔬菜中引发严重的枯萎病。在本研究中,我们通过16S rRNA PCR扩增从木瓜枯萎病中鉴定出[病原体名称未给出]。通过扩增约1500 bp的[基因名称未给出]基因清晰条带确定了[病原体名称未给出]的致病能力。此外,[病原体名称未给出]种子发芽试验表明,[病原体名称未给出]分别使黄瓜、瓠瓜和南瓜种子的发芽率降低了26.21%、34%和33.63%,同时地上部和根部生长也显著减少。此外,使用药用植物的抗菌化合物记录了[病原体名称未给出]的生长抑制情况,[植物名称未给出]的石油醚根提取物显示出最高22±0.04 mm的抑菌圈直径,而[植物名称未给出]的甲醇提取物和[植物名称未给出]的乙醇提取物对[病原体名称未给出]的抑菌圈分别为20±0.06 mm和20±0.01 mm。此外,[植物名称未给出]的生物活性化合物通过产生17±0.09 mm的抑菌圈抑制了[病原体名称未给出]的生长。为了揭示抑制机制,我们采用了化学-蛋白质相互作用网络和分子对接方法,发现[植物名称未给出]中的芦丁与[病原体名称未给出]的柠檬酸(Si)合酶和二氢硫辛酰胺脱氢酶相互作用,结合亲和力为-9.7 kcal/mol和-9.5 kcal/mol,而[植物名称未给出]中的槲皮素与[病原体名称未给出]的必需蛋白F0F1 ATP合酶α亚基相互作用,结合亲和力为-6.9 kcal/mol并抑制了[病原体名称未给出]的生长。我们的研究将为木瓜枯萎病的生态友好型生物防治开发提供启示。