拮抗枯草芽孢杆菌KC-5的分离鉴定及其发酵优化

为了筛选出对植物病原菌具有拮抗作用的生物防治细菌,采用平板对峙法从蔬菜根际土壤中分离获得一株对多种病原真菌具有抑制作用的枯草芽孢杆菌,并对抑制后的病原菌菌丝进行了观察,结果表明该菌株对尖孢镰刀菌、串珠镰刀菌、层出镰刀菌以及腐皮镰刀菌均具有抑菌活性。通过形态特征、生理生化特征及16S rRNA序列分析,将该菌株鉴定为枯草芽孢杆菌(Bacillus subtilis),并对其发酵培养基进行了优化。     

内生真菌司氏角担子菌B6对尖孢镰刀菌西瓜专化型菌株的拮抗作用

近年来,尽管西瓜产业不断发展壮大,但轮作土壤种植西瓜易产生枯萎病害导致世界范围内的西瓜严重减产。通过对峙培养实验和抑菌实验探讨了重阳木内生真菌司氏角担子菌(Ceratobasidum stevensii)B6菌株对西瓜枯萎病病原菌尖孢镰刀菌西瓜专化型(Fusarium oxysporum f. sp.Niveum,FON)的拮抗作用,并初步分析了其作用机制。平板拮抗试验的结果表明,内生真菌B6生长过程中不是通过产生抑菌带来抑制FON菌丝,而是利用自身的生长优势将FON完全覆盖。显微观察B6与FON菌丝的接触部位,发现FON菌丝外侧附着B6顶端菌丝形成的胞样结构,表明FON菌丝生长仅受到B6菌丝的抑制。抑菌试验结果显示,B6产生的挥发性物质可以抑制FON的生长和产孢,并使其菌丝分枝明显减少;B6的发酵液对FON的生长和产孢没有抑制作用。因此,推测B6主要通过释放某些挥发性物质产生拮抗作用而抑制FON的生长。     

香芹酚和丁香酚对腐皮镰刀菌的抑菌活性及抑菌机理

【背景】腐皮镰刀菌(Fusarium solani)是世界上最具破坏性的土传病原菌之一,严重影响作物的产量及品质。因此寻找并开发广谱的可持续生物防治药剂迫在眉睫,而植物次级代谢物为自然界筛选生物源天然杀菌剂提供了丰富的原料。【目的】研究香芹酚和丁香酚对腐皮镰刀菌的抑菌活性,探究其可能涉及的抑菌机理。【方法】采用菌丝生长速率法、十字交叉法和孢子萌发法分析香芹酚和丁香酚对菌丝和孢子的抑制活性,通过扫描电镜(scanning electron microscope,SEM)观察菌丝微观形态的变化,利用荧光染料碘化丙啶(propidium iodide,PI)观察细胞膜的损伤情况,并测定其对腐皮镰刀菌细胞膜胞外电导率、蛋白质含量和麦角固醇合成的影响。【结果】香芹酚和丁香酚对腐皮镰刀菌菌丝生长和孢子萌发均有显著的抑制效果,并呈现剂量依赖效应,EC50值分别为92.39μL/L和263.00μL/L。SEM结果表明,2种精油处理腐皮镰刀菌后,其细胞壁和细胞膜均遭到破坏从而不能维持菌丝正常的线性形态,表现出不同程度的弯曲、褶皱和凹陷。PI染色结果发现,2种精油处理严重破坏了腐皮镰刀菌细胞膜的完整性和...     

一株新的拮抗细菌SL19及其抑菌活性物质

生防菌SL19对多种植物病原菌有抑菌活性。通过形态观察、生理生化实验和基于16S rDNA同源性序列分析构建系统发育树,鉴定该菌为Bacillus velezensis。利用对峙实验测定了该菌的抑菌谱,发现该菌对大丽轮枝菌、尖孢镰刀菌、灰葡萄孢菌、立枯丝核菌、疮痂链霉菌等多种植物病原微生物有明显的抑菌作用。利用硫酸铵盐析法分离纯化活性物质,并对其理化性质进行初步探索显示:抑菌活性物质经60°C、80°C处理20 min后的抑菌活性不变;经100°C处理20 min,活性降低为原来的75.3%;经120°C处理20 min后抑菌活性完全丧失。对胰蛋白酶、胃蛋白酶、蛋白酶K、氯仿、紫外光均不敏感,SDS-PAGE检测发现该抑菌活性物质中含有分子量约为50 kD的蛋白质,初步推测该菌分泌的抑菌活性物质主要是蛋白质类物质。实验表明,该抗菌蛋白能够抑制大丽轮枝菌菌丝的生长及孢子的萌发,为该菌用于生物防治提供了理论基础。     

对镰刀菌有抗菌作用的硝基丙烷化合物

室内试验中测定了硝基丙烷化合物(药剂代号791224)对植物病原菌和镰刀菌的抗菌作用。791224对棉花枯萎病菌和小麦赤霉病菌菌丝生长的抑制作用明显优于其他供试植物病原菌。791224对所有供试镰刀菌均显示了优异的抗菌活性。791224浓度为5 ppm时,对供试的12种镰刀菌菌丝生长抑制效果平均在54.2—100%,对砖红镰刀菌的抑菌活性为100%,而相同浓度的多菌灵抑菌活性前者为0—27.3%,后者为0%,即低2.7—100倍。791224对由腐皮镰刀菌引起的国槐立枯病的防治效果也极为显著。     

一株链霉菌21-1的分离鉴定及其对禾谷镰刀菌的抑菌活性

【背景】由禾谷镰刀菌(Fusarium graminearum)引起的小麦赤霉病严重威胁我国的小麦生产。【目的】筛选对禾谷镰刀菌具有拮抗能力的链霉菌菌株,为生防菌剂开发提供理论基础。【方法】利用平板对峙法筛选对禾谷镰刀菌具有拮抗能力的链霉菌;通过形态特征、生理生化特征和16S rRNA基因序列分析对其进行鉴定;通过病原菌菌丝生长、孢子产生及萌发抑制试验分析其发酵液的抑菌活性;利用人工接种试验测定该菌株发酵液的防病效果。【结果】筛选到一株对禾谷镰刀菌具有较强拮抗活性的链霉菌21-1,抑菌率为59.5%。依据形态特征、生理生化特性和16S rRNA基因序列分析,将该菌株鉴定为黄三素链霉菌(Streptomycesflavotricini)。菌株21-1发酵液能够抑制禾谷镰刀菌的菌丝生长、孢子产生及萌发过程,而且可以降低禾谷镰刀菌菌丝中可溶性蛋白质的含量,并增加丙二醛的含量。菌株21-1可以产生蛋白酶及纤维素酶。菌株21-1菌液10倍稀释液对小麦赤霉病的防效最佳,为70.1%。此外,菌株21-1发酵液对其他8种植物病原菌均有较好的抑制作用。【结论】菌株21-1对禾谷镰刀菌有较好的抑菌活性,具...     

独蒜兰提取物对植物病原真菌的抑菌活性

【目的】研究独蒜兰假鳞茎乙醇提取物对植物病原真菌的抑菌作用,为植物源杀菌剂的开发提供依据。【方法】采用菌丝生长速率法,研究独蒜兰假鳞茎乙醇提取物对15种植物病原菌的抑制活性;以西瓜尖孢镰刀菌作为供试菌,进一步研究该提取物对病原真菌的菌丝干重、细胞膜、过氧化氢酶（CAT）、过氧化物酶（POD）和超氧化物歧化酶（SOD）等的影响。【结果】独蒜兰假鳞茎提取物对辣椒疫霉病菌、西瓜尖孢镰刀菌、番茄灰霉病菌和非洲隐地疫霉菌的抑菌效果明显,其EC₅₀值分别为0.849、0.782、0.813和1.161 mg·mL^-1;经独蒜兰提取物处理后的西瓜尖孢镰刀菌菌丝干重随着药剂浓度的增加而减少;细胞膜丙二醛含量和相对电导率增加;菌丝体细胞内CAT、POD和SOD 3种保护酶活性增加。【结论】独蒜兰假鳞茎提取物对植物病原真菌具有较好的抑菌活性,其抑菌作用可能与其干扰菌丝生长、使菌丝细胞膜正常功能受损等有关。     

枯草芽孢杆菌对几种植物病原真菌的抑菌活性

枯草芽孢杆菌是目前国内外比较具有应用潜力的生防菌种之一。本文主要研究了枯草芽孢杆菌菌液对几种植物病原菌的菌丝抑制试验、菌丝形态影响试验以及分生孢子萌发抑制试验,了解枯草芽孢杆菌菌液对尖孢镰刀菌古巴专化型、灰葡萄孢、茄病镰刀菌、大丽轮枝菌、麦根腐平脐蠕孢、尖孢镰刀菌的抑制作用及抑菌机理。结果显示:枯草芽孢杆菌菌液对6种病原真菌的菌丝形态、菌丝生长、产孢和分生孢子萌发都有明显的破坏或抑制作用。用枯草芽孢杆菌菌液处理尖孢镰刀菌古巴专化型、灰葡萄孢、茄病镰刀菌、大丽轮枝菌、麦根腐平脐蠕孢、尖孢镰刀菌后,在PDA培养基上均形成了明显的抑菌圈,直径达3. 00 cm左右;菌液处理后分生孢子的萌发率仅30%左右。显微镜观察发现,处理组菌丝生长异常,体表凹凸不平,局部膨大,分枝变多,原生质体外泄。研究表明枯草芽孢杆菌菌株对尖孢镰刀菌古巴专化型、灰葡萄孢、茄病镰刀菌、大丽轮枝菌、麦根腐平脐蠕孢和尖孢镰刀菌有良好的抑制作用,并且可以有效控制尖孢镰刀菌古巴专化型、灰葡萄孢、茄病镰刀菌、大丽轮枝菌、麦根腐平脐蠕孢和尖孢镰刀菌病害的发生。     

S-159-06菌株活性产物对植物病原菌的抑菌谱及拮抗机理初探

对S-159-06菌株活性产物的抑菌谱及其拮抗机理作了初步研究,结果表明：S-159-06活性产物具有较广的抑菌谱,对多种病原真菌和细菌具有较好的抑制作用;S-159-06活性产物能强烈抑制病原菌菌丝的生长和孢子的萌发,可引起病原菌菌丝扭曲,菌丝膨大成串珠状,分枝增多,分枝顶端膨胀后细胞壁破裂,原生质外溢,产生溶菌作用;使分生孢子数减少,孢子萌发畸形,萌发率降低;在温室条件下,S-159-06活性产物不仅能阻止番茄灰霉病菌菌丝的入侵,而且在植物体内有内吸作用,对已侵入的菌丝有较好的治疗作用。     

实验培养红菇对肠道致病菌的抑菌活性研究

研究实验条件下培养红菇菌丝和发酵液对几种肠道致病菌的抑菌活性。结果发现其对大肠埃希菌具有特异性抑制,对其他菌的抑制较弱。初步确定了最小抑菌活性,认为红菇多糖具有一定的抑菌潜力。     

Hydrodynamic, physiological, and morphological characteristics of Fusarium moniliforme in geometrically dissimilar stirred bioreactors

The influence of two mixing geometries (at the same scale) with different flow energy distributions on the performance of the gibberellic acid fermentation and on the morphology of the producing fungus Fusarium moniliforme was investigated. Fermentations were performed using a turbine mixing system (TMS) and a counterflow mixing system (CMS), which were high and low power number mixing systems, respectively. Different agitator speed rate profiles were maintained to obtain equal specific power inputs to both mixing systems. Substantial differences in morphology and productivity of F. moniliforme were found. To investigate the causes of these differences, local values and spectra of the kinetic energy of flow fluctuations were measured during the fermentations using a stirring intensity measuring device (SIMD) and a frequency spectrum analyzer. Biomass and gibberellic acid concentrations were found to be higher in the TMS, where the energy distribution was less even, and Vi/here the main part of the energy was at small frequencies (large eddies). An automated image analysis method was used for quantitative characterization of F. moniliforme freely dispersed mycelia and clump morphology. A higher proportion of clumped mycelia with clumps of larger area, perimeter, and roughness was observed in the TMS. A correlation between the morphology and productivity was found, and TMS favored the development of more productive mycelia with longer and thinner hyphae. Introduced power was not a good parameter to characterize different impellers, even at a given scale. (c) 1995 John Wiley & Sons, Inc.     

Fengycin antibiotics isolated from B-FS01 culture inhibit the growth of Fusarium moniliforme Sheldon ATCC 38932

Strain B-FS01, isolated from rape (Brassica napus) stem infected by Slerotinia sclerotiorum and identified as Bacillus subtilis, exhibited predominantly antagonistic activities against Fusarium moniliforme Sheldon ATCC 38932. Antifungal active compounds (AAC) were isolated and purified from the cultures of strain B-FS01 against ATCC 38932. The HPLC/electron spray ionization/collision-induced dissociation mass spectrum of AAC revealed a cluster of fengycin homologues containing fengycins A, fengycins B and a new type of fengycin. Further toxic assay of AAC in vitro against F. moniliforme indicated that AAC could strongly inhibit the growth of both mycelia and spores. In addition, treatment with AAC significantly modified the maize seed infection by ATCC 38932.     

Dimorphic fungus characteristic of fumonisin-producing strains of Fusarium moniliforme from Zhejiang

Fusarium moniliforme and its fumonisins have been shown to be carcinogenic in lab animals and have been linked to high incidences of human esophageal cancer. In this study we report the dimorphic fungus characteristic of fumonisin-producing strains of F. moniliforme from foodstuffs in Zhejiang, China. All of the twenty strains of F. moniliforme shown produce fumonisin B₁ 475.9–6322.2 μg/g in corn medium. These strains of F. moniliforme form yeast-like colonies in Sabouraud's agar plates contained 9% NaCl at 37 °C incubator and shows mostly budding reproduction. In blood agar plates these strains of F. moniliforme appear grass-green haemolytic reactions. This is the first report that yeast-like growth, dimorphic pathogenic fungus feature is found in F. moniliforme. These results suggest that it is also important to program epidemiological surveys of F. moniliforme as a primary pathogenic fungus, while proceeding to produce mycotoxins of F. moniliforme in food hygiene. This revised version was published online in August 2006 with corrections to the Cover Date.     

Efficacy of ammonia in detoxification of fumonisin contaminated corn

Fumonisin B1 level in culture material and in naturally contaminated corn by F. moniliforme was reduced by 30 and about 40%, respectively, by ammonia treatment. Atmospheric ammoniation of corn did not appear to be an effective method for detoxification of F. moniliforme contaminated corn.     

Moniliformin production and toxicity of different Fusarium species from Southern Africa.

Four new moniliformin-producing species of Fusarium were found, viz., F. acuminatum, F. concolor, F. equiseti, and F. semitectum. Isolates of F. acuminatum and F. concolor produced large amounts of moniliformin (3.4 and 9.5 g/kg, respectively), whereas isolates of the other three species yielded less than 30 mg/kg. The production of moniliformin by isolates of F. oxysporum and F. avenaceum from southern Africa is described. All 14 toxic isolates of F. oxysporum produced moniliformin. Most isolates of F. fusarioides and all six isolates of Fusarium moniliforme va. subglutinans tested produced moniliformin, as did 28 of 36 toxic isolates of F. moniliforme. A number of F. moniliforme isolates produced greater than 10 g/kg, and one isolate yielded 33.7 g/kg in corn after incubation for 5 weeks at 25 degrees C. Moniliformin production in the field in corn ears was shown by inoculating plants with known moniliformin-producing isolates of three Fusarium species. Yields of up to 645 mg/kg were recorded. Isolates of F. acuminatum, F. equiseti, F. fusarioides, and F. moniliforme were found that were highly toxic to ducklings but which did not produce moniliformin.     

Identity of Fusarium nygamai isolates with long and short microconidial chains from millet,sorghum and soil in Africa

Several Fusarium species have been found associated with millet and sorghum in Nigeria, Lesotho and Zimbabwe. Amongst these, some isolates were originally identified as short- and long-chained types of F. nygamai. However, there was some question as to the correct identification of the long chained types. This study reclassified some of the isolates with long microconidial chains as F. moniliforme. Morphologically, these strains do not produce chlamydospores like F. nygamai, but produce swollen hyphal cells or resistant hyphae. The isolates in this study were crossed with the mating-type tester strains of Gibberella fujikuroi (F. moniliforme and G. nygamai (F. nygamai). Of the isolates with long chains of microconidia and other characteristics of F. moniliforme, 36% crossed with mating population 'A' of G. fujikuroi. Of the isolates with characteristics of F. nygamai, 65% crossed with the testers used to produce the teleomorph of F. nygamai. Mating tests support the separation of the sample population into F. moniliforme and F. nygamai. The results of this study show that genetics can be an aid in resolving some problems in fungal taxonomy. This revised version was published online in August 2006 with corrections to the Cover Date.     

水稻恶苗病菌对苯并咪唑类杀菌剂抗药性分子机理研究初探

用真菌β-微管蛋白基因的丰余寡聚核着酸引物B1和B3,扩增了一段871bp的水稻恶苗病菌Fusariummoniliforme的β微管蛋白基因片段,进行了克隆和DNA序列测定,并根据该序列设计了Fmoniliformeβ-微管蛋白基因的特异性测序引物。经过对恶苗病菌对多菌灵具有不同抗性水平菌株的β-微管蛋白基因核着酸序的比较研究,表明Fmoniliforme的β微管蛋白的165,198,200和257位置氨基酸末发生突变,在克隆的片段内也未发现能引起氨基酸改变的核着酸突变。说明该菌对多菌灵产生抗性的分子机理与目前已知的其他真菌有所不同,有待进～步研究。     

Survey of fumonisin production by Fusarium species

Fumonisins B1 (FB1) and B2 (FB2), two structurally related mycotoxins with cancer-promoting activity, were recently isolated from corn cultures of Fusarium moniliforme MRC 826. These toxins have been reported to be produced also by isolates of F. proliferatum. Contamination of foods and feeds by F. moniliforme has been associated with human esophageal cancer risk, and FB1 has been shown to be the causative agent of the neurotoxic disease leukoencephalomalacia in horses. Because of the toxicological importance of the fumonisins, the potential to produce FB1 and FB2 was determined in a study of 40 toxic Fusarium isolates representing 27 taxa in 9 of the 12 sections of Fusarium, as well as two recently described species not yet classified into sections. With the exception of one isolate of F. nygamai, fumonisin production was restricted to isolates of F. moniliforme and F. proliferatum, in the section Liseola. The F. nygamai isolate produced 605 micrograms of FB1 g-1 and 530 micrograms of FB2 g-1, and the identity of the toxins was confirmed by capillary gas chromatography-mass spectrometry. This is the first report of the production of the fumonisins by F. nygamai.     

Microbiological Aspects in the Hydroxylation of Estrogens by Fusarium moniliforme

A strain of Fusarium moniliforme (IH4), isolated from soil, showed outstanding enzymatic abilities to hydroxylate a number of estrogens. Estrone and estradiol were transformed into the 15alpha-hydroxy derivatives, and estradiol 3-methyl ether was transformed into the corresponding 6beta-hydroxy derivative. Delta(6)-Estrone was not hydroxylated. The accumulation of 15alpha-hydroxyestrone was influenced by the nutritional conditions of the fungus. Maximal yield was obtained when the organism grew in Czapek solution supplemented with yeast extract, although good conversion was also found in a peptone-corn molasses medium. Substitution of NO(3)-N in Czapek medium with NH(4)-N, lactalbumin hydrolysate, Casitone, or Casamino Acids resulted in limited hydroxylation of estrone. A remarkable strain specificity was demonstrated in this conversion. Of 13 strains of F. moniliforme and Gibberella fujikuroi under investigation, only 2 strains (IH4 and ATCC 9851) accumulated substantial amounts of the 15alpha-hydroxylated product. However, marked quantitative variations were observed which are attributable to a different ability of the organisms to degrade the steroid nucleus. Biochemical instabilities were also found through the appearance of spontaneous variants lacking steroid-hydroxylating activity. Replacement culture studies revealed that 15alpha-hydroxylation of estrone was dependent on the supply of external phosphate; exogenous nitrogen or energy sources were not required. Most of the enzymatic activity was confined to the mycelia. Microconidia showed a very limited hydroxylating activity, even in the presence of supplements or energy sources.