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Mycologia. 2022 Jan-Feb;114(1):24-34. doi: 10.1080/00275514.2021.1990627. Epub 2021 Dec 20.
3
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Terretonin D1, a new meroterpenoid from marine-derived ML-44.特瑞醇 D1,一种新型海洋来源 ML-44 衍生的倍半萜烯类化合物。
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New butenolide derivatives from the marine sponge-derived fungus Aspergillus terreus.源自海洋海绵衍生真菌土曲霉的新型丁烯内酯衍生物。
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Antagonistic studies and hyphal interactions of the new antagonist Aspergillus piperis against some phytopathogenic fungi in vitro in comparison with Trichoderma harzianum.新拮抗真菌胡椒拟青霉与哈茨木霉对几种植物病原菌的拮抗作用及其菌丝亲和性的比较研究
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Isolation and identification of nematode-antagonistic compounds from the fungus Aspergillus candidus.从亮白曲霉中分离和鉴定对线虫具有拮抗作用的化合物
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灰绿曲霉对柱隔孢属的拮抗活性。

Antagonistic activity of Aspergillus versicolor against Macrophomina phaseolina.

机构信息

Department of Plant Pathology, Faculty of Agricultural Sciences, University of the Punjab, Quaid-i-Azam Campus, Lahore, 54590, Pakistan.

出版信息

Braz J Microbiol. 2022 Sep;53(3):1613-1621. doi: 10.1007/s42770-022-00782-6. Epub 2022 Jul 13.

DOI:10.1007/s42770-022-00782-6
PMID:35831780
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9433477/
Abstract

The present study was carried out to evaluate the antagonistic efficacy of Aspergillus versicolor against the soil and seed inhibiting destructive plant pathogen Macrophomina phaseolina. The tested antagonist was confirmed by rDNA sequencing of ITS and β-tubulin genes with respective accession numbers MN719083 and MN736397. In dual culture bioassays, A. versicolor showed potent antagonist activity and reduced the pathogen's growth by 60% over control. To understand the mechanism of antagonistic fungus, DNA of the pathogenic fungus was incubated in secondary metabolites produced by the A. versicolor for 24 and 48 h. After 48 h, metabolites of A. versicolor fully degraded the DNA of M. phaseolina. Moreover, for the identification of bioactive compounds, the chloroform and ethyl acetate fractions of A. versicolor culture filtrates were subjected to GC-MS analysis. A total of 10 compounds were identified in each of the two fractions. Among these, chondrillasterol (37.43%) followed by 1,2-benzedicarboxylic acid, diisooctyl ester (25.93%), decane (16.63%), 9,12-octadecadienoic acid (Z,Z)- (13.32%), stigmasterol (11.16%), undecane (10.93%), cis-1-chloro-9-octadecene (8.66%), benzene, 1,3,5-trimethyl (8.46%), and hexadecanoic acid, 2-hydroxy-1-(hydroxymethyl) ethyl ester (8.13%) were the major compounds. Some of the identified compounds are known to possess strong antifungal, antibacterial, nematicidal, and antioxidant properties. The present study concludes that A. versicolor is an effective antagonist against M. phaseolina.

摘要

本研究旨在评估土曲霉(Aspergillus versicolor)对土壤和种子抑制性破坏性植物病原菌(Macrophomina phaseolina)的拮抗功效。通过 ITS 和β-微管蛋白基因的 rDNA 测序对受试拮抗菌进行了确认,相应的登录号分别为 MN719083 和 MN736397。在双层培养生物测定中,土曲霉表现出强烈的拮抗活性,使病原菌的生长比对照减少 60%。为了了解拮抗真菌的作用机制,将致病真菌的 DNA 与土曲霉产生的次级代谢产物在孵育 24 和 48 小时。48 小时后,土曲霉的代谢物完全降解了 M. phaseolina 的 DNA。此外,为了鉴定生物活性化合物,对土曲霉培养滤液的氯仿和乙酸乙酯馏分进行了 GC-MS 分析。在这两个馏分中,每个馏分都鉴定出了 10 种化合物。在这些化合物中,角鲨烯(37.43%),其次是 1,2-苯二甲酸、二异辛酯(25.93%)、癸烷(16.63%)、(Z,Z)-9,12-十八碳二烯酸(13.32%)、豆甾醇(11.16%)、十一烷(10.93%)、顺式-1-氯-9-十八烯(8.66%)、苯、1,3,5-三甲基(8.46%)和十六烷酸、2-羟基-1-(羟甲基)乙酯(8.13%)是主要化合物。一些已鉴定的化合物具有很强的抗真菌、抗菌、杀线虫和抗氧化特性。本研究得出结论,土曲霉是 M. phaseolina 的有效拮抗物。