24 resultados para Fusarium pallidoroseum


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通过对江苏省云台山地区7种不同野生中草药植物烟台百里香(T.quinquecostatusCelak.)、掌叶半夏(P.pedatisectaSchott.)、何首乌(P.multiflorumThunb.)、海洲香薷(E.splendensNakai ex F.)、野葛[P.lobata(Willd)Ohwi]、紫金牛(A.japonicaBl.)和菝葜(S.sieboldiiMiq.)根区土壤真菌进行分离鉴定,共分离出真菌16属126种。多样性分析结果表明,7种野生中草药植物根区土壤真菌种群多样性丰富,其中青霉属(Penicillium)、曲霉属(Asper-gillus)和木霉属(Trichoderma)是中草药植物根区土壤中的优势种群,镰孢菌属(Fusarium)、交链孢属(Alternaria)、腐霉属(Pythium)、毛霉属(Mucor)真菌分布丰度也较高。结果也表明根区土壤真菌群落在一定程度上受到中草药植物的影响,大部分野生中草药植物根区土壤的真菌群落的均匀度指数低于裸地非根区土壤,而丰富度指数却高于裸地非根区土壤。不同野生中草药植物根区土壤真菌区系的结构和组成存在一定的差异性,紫金牛根区土壤中真菌种类最多,达到14属,而野葛根区土壤中真菌种类最少,只有8属。

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采用莲藕状聚乙烯醇复合载体对镰刀菌(Fusarium sp.)固定化包埋,分别进行了不同接种量的固定化真菌对菲、芘的降解,固定化真菌对不同系列浓度菲、芘的降解试验,以及对固定化真菌在自然土壤中对菲、芘降解的各项参数作了测定,结果表明,固定化真菌具有较好的降解效果,同时用电镜观察研究了镰刀菌在固定化载体中的分布形态.自然土壤中固定化真菌在360h时,对菲、芘的降解效率分别为76.96%和20.69%,而土著菌仅达到33.37%和15.28%.

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目的:探索牛蒡根际镰刀菌与牛蒡之间的相互关系。方法:从全国30个地区采集牛蒡根际土壤样品,进行了根际土壤真菌数量和群落的生态学研究,测定镰刀菌发酵液对牛蒡幼苗和牛蒡子萌发的影响,并对其中毒性最强的两株镰刀菌F130和F131进行了形态学和分子生物学的鉴定。结果:镰刀菌为牛蒡根际的最优势类群,贡献率为34.297%,其次为木霉,贡献率为22.519%;绝大多数镰刀菌对牛蒡有明显的毒性作用,其中F130和F131被鉴定为Fusarium solani。结论:Fusarium solani是牛蒡根际土壤中的致害菌。

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尖孢镰刀菌萎蔫专化型(Fusarium oxysporumf.sp.vasinfectum,SF2)及其分泌的毒素是造成杉木连栽土壤中毒的重要因素之一,基于此,笔者从106株海洋微生物中筛选到23株具有拮抗SF2特性的菌株,在湖南会同杉木中心产区进行的室外盆栽试验结果表明,其中海洋细菌3728菌株能够在杉木根际土壤中定殖,抑制杉木致害菌的生长繁殖,促进了杉木幼苗生长,经鉴定为枯草芽孢杆菌(Bacillus subtilis)。该研究对杉木人工林生产具有重要的理论与实践意义。

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利用微生物对石油污染土壤进行生物降解,具有操作简单,费用低廉,场地适用性强等特点。挑选了2种菌株,进行了室内油降解实验,在摇床实验油降解率:微生物真菌(Faserium.LK)(土著)和真菌(Phanerochaete.Chrysosprium),在20d分别为41.2%和28.1%,真菌(Fusarium.LK)高于真菌(Phane-rochate.Chrysosprium)的降解率,而在培养箱石油污染土壤中,真菌(Fusarium.LK)(土著)和真菌(Phane-rochaete.Chrysosprium),在50d分别为61.8%和66.1%,(Fusarium.LK)低于(Phanerochaete.Chrysosri-um)。

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In this communication, biosynthesis of gold nanoparticles assisted by Escherichia coli DH5 alpha and its application on direct electrochemistry of hemoglobin are reported. The gold nanoparticles formed on the bacteria surface are mostly spherical. The direct electrochemistry of hemoglobin can be achieved by incorporated into the bio-nanocomposite films on a glassy carbon electrode.

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In this paper, 20 kinds of different 2-(alpha-arylamino phosphonate)-chitosan (2-alpha-AAPCS) were prepared by different Schiff bases of chitosan (CS) reacted with di-alkyl phosphite in benzene solution. The structures of the derivatives (2-alpha-AAPCS) were characterized by FT-IR spectroscopy and elemental analysis. In addition, the antifungal activities of the derivatives against four kinds of fungi were evaluated in the experiment. The results indicated that all the prepared 2-alpha-AAPCS had a significant inhibiting effect on the investigated fungi when the derivatives concentration ranged from 50 to 500 mu g mL(-1). Furthermore, the antifungal activities of the derivatives increased with increasing the molecular weight and concentration. And the antifungal activities of the derivatives were affected by their dimensional effect and charge density. Besides, the rule and mechanism of the antifungal activities of them were discussed in this paper. (C) 2009 Elsevier B.V. All rights reserved.

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Three different acyl thiourea derivatives of chitosan (CS) were synthesized and their structures were characterized by FT-IR spectroscopy and elemental analysis. The antimicrobial behaviors of CS and its derivatives against four species of bacteria (Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Sarcina) and four crop-threatening pathogenic fungi (Alternaria solani, Fusarium oxysporum f. sp. vasinfectum, Colletotrichum gloeosporioides (Penz.) Saec, and Phyllisticta zingiberi) were investigated. The results indicated that the antimicrobial activities of the acyl thiourea derivatives are much better than that of the parent CS. The minimum value of MIC and MBC of the derivatives against E coli was 15.62 and 62.49 mu g/mL, respectively. All of the acyl thiourea derivatives had a significant inhibitory effect on the fungi in concentrations of 50 - 500 mu g/mL; the maximum inhibitory index was 66.67%. The antifungal activities of the chloracetyl thiourea derivatives of CS are noticeably higher than the acetyl and benzoyl thiourea derivatives. The degree of grafting of the acyl thiourea group in the derivatives was related to antifungal activity; higher substitution resulted in stronger antifungal activity. (c) 2007 Elsevier Ltd. All rights reserved.

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Three kinds of Schiff bases of carboxymethyl chitosan (CMCTS) were prepared, and their antifungal activities were assessed according to Jasso de Rodriguez's method. The results indicated that 2-(2-hydroxybenzylideneamino)-6-carboxymethylchitosan (HNCMCTS) and 2-(5-chloro-2-hydroxybenzylideneamino)-6-carboxymethylchitosan (HCCMCTS) had better inhibitory effects than those of chitosan or CMCTS against Fusarium oxysporium f. sp. vasinfectum, Alternaria solani, and Valsa mali. (c) 2005 Elsevier Ltd. All rights reserved.