辣椒炭疽病菌生物学特性的研究

辣椒炭疽病菌在不同培养基中培养,以PDA、PCA、CFA、CLA菌丝生长最佳,在CMA、PDA、CFA中产孢量最多。病原菌生长和产孢的最适温度和pH值分别为26—28℃和pH4.5—6.5,自然散光和完全黑暗有利于菌丝生长,12小时黑光灯与12小时黑暗交替处理有利于产孢。该菌对多种碳源和氮源均可利用,其中木糖、葡萄糖和蔗糖作碳源,天冬酰胺作氮源,菌生长和产孢最佳。分生孢子在25℃,pH6.0—8.0,相对湿度100%,黑光灯照射,以及20%辣椒叶煎汁或1%蛋白胨液中,萌发率最高,其致死温度为50℃处理10     

绣球菌生物学特性若干问题的研究

绣球菌菌丝在蛋白胨培养基中生长最佳,硫酸铵、尿素、复合肥对菌丝生长有抑制作用。选用基础培养基或在基础培养基中添加0.3%蛋白胨作为绣球菌母种培养基较为合适。栽培料中添加淀粉可促进绣球菌的生长,接种50d后观察发现,添加新鲜去皮马铃薯块比马铃薯淀粉效果好,前者100%菌袋出现原基,后者只有50%菌袋出现原基,且原基正处在胶质片时期。添加大米淀粉,小麦淀粉效果与马铃薯块接近,甘薯淀粉与马铃薯淀粉效果接近。     

甘蓝根肿病菌的生物学特性研究

对甘蓝根肿病菌生物学特性研究表明,该菌休眠孢子萌发的最适温度24℃,最适pH值6.0-6.7,致死温度45℃,肿根腐烂处理可以显著提高萌发率,光对休眠孢子萌发有明显抑制作用。该菌休眠孢子在感病寄主的根分泌物溶液中萌发率最高,达75％,耐病甘蓝品种及番茄的根分泌物均能刺激休眠孢子萌发。通过电镜观察,根肿病菌休眠孢子为近球形,孢壁有乳状突起,直径2.1-3.1μm（平均直径2.5μm)。游动孢子为近球形或椭圆形,大小为1.6-3.6μm。同侧着生不等长尾鞭式双鞭毛。     

木霉菌T25生物学特性的研究

温度对T25菌株菌丝生长和孢子产生影响显著,30℃时菌丝生长最快,25℃时产孢量最大。T25在pH值2~10范围内均可生长,pH值5~6时生长最快,pH值为6时孢子产生量最大。光照处理对菌丝生长影响显著,并且明显促进孢子产生。淀粉、蔗糖分别为菌丝生长和产孢的最佳碳源。硫酸铵和蛋白胨为菌丝生长和产孢的最佳氮源。不同维生素对菌丝生长和孢子产生的作用不同,VB1 VH、VB6对菌丝生长和产孢最有利。微量元素对菌丝生长有一定的促进作用,Ca2 有利于孢子的产生。     

芒果褐色蒂腐病菌(Phomopsis mangiferae)生物学特性研究

从广西芒果病区分离出芒果褐色蒂腐病菌 (Phomopsismangiferae) ,对其生物学特性进行的研究结果表明 ,该病菌的最适生长温度为 2 5～ 31℃ ;最适生长 pH值为 6 .0～ 6 .5 ;不同光环境对分生孢子器形成的影响较大 ,其中黑光最利于分生孢子器的形成 ;多菌灵对该病菌的室内抑制作用最强     

黑木耳8808菌株生物学特性研究

黑木耳8808菌株,是笔者几年来,从黑龙江省15个地区,采集的32个样本中,分离的59个野生菌株中,经多次培养、比较,栽培试验选出的一株优质、高产菌株。该菌株1992年,在本省五常县长山乡生产150万袋,全省生产近1000万段,均获丰收,产量、质量均明显优于原生产菌株。为更好的为生产提供科学依据,本文研究了该木耳孢子弹射及萌发特征,菌丝、子实体、孢子形态,不同温度、pH、氮碳源浓度,不同培养料配方对该木耳菌丝生长及产实影响。     

马铃薯干腐病菌硫色镰孢的生物学特性

从碳源、氮源、酸碱度及生长温度等方面对引起马铃薯干腐病的硫色镰孢Fusarium sulphureum的生物学特性进行了研究。结果表明,该病原菌在不同发育阶段对营养和环境条件的要求存在差异。在固体培养基上,菌落生长最佳碳源为葡萄糖、麦芽糖,最佳氮源为蛋白胨,pH8?为最佳;在液体培养基中,菌丝体生长以麦芽糖为最佳碳源,以硝酸钠为最佳氮源,pH6?为最佳;在分生孢子萌发阶段,在以羧甲基纤维素钠、蛋白胨和谷氨酸为碳、氮源的营养液中,分生孢子萌发率最高,最适pH 6–8。该病菌最适生长温度为25℃,分生孢子致死     

天麻萌发菌株的生物学特性研究

对4个天麻种子萌发菌菌株在不同培养条件下菌丝的生长进行了研究。结果显示,4个天麻萌发菌的最佳生长温度为25℃,适宜生长的pH值范围为5.0~6.0,最佳培养基为木屑-麸皮培养基。综合试验结果筛选出西乡为一株优良天麻萌发菌。     

白藜芦醇对核桃细菌性黑斑病菌的抑制作用

旨为核桃细菌性黑斑病天然杀菌剂的开发提供理论依据,同时为白藜芦醇在农林作物病害防治上的应用奠定基础.测定了白藜芦醇对核桃细菌性黑斑病菌(Xaj)的最低抑菌浓度(MIC)和最低杀菌浓度(MBC).在白藜芦醇的亚抑菌浓度下,开展了以下实验:(1)通过结晶紫染色法检测了Xaj生物膜的形成;(2)测定了胞外多糖的产生量;(3)...     

Mycelium of Alternaria alternata as a potential biological control agent for Eupatorium adenophorum

The fungus, Alternaria alternata (Fr.) Keissler Strain 501, has been evaluated as a bioherbicide for control of Eupatorium adenophorum Spreng., but the biology of the pathogen–host interaction and the optimal environmental conditions for disease development and effective weed control are unknown. Disease development of A. alternata Strain 501 mycelia on E. adenophorum was assessed under several factors including pathogen inoculum concentration, plant age, dew period duration, post-dew temperature, storage temperature and duration. The minimum inoculum concentration required to kill E. adenophorum seedlings was 3.2×10⁶ mycelial fragment mL^?1. E. adenophorum seedlings at the four-leaf-pair stage were more susceptible than the older plants, especially those at the older than seven-leaf-pair stage. With a dew period of at least 14 h, 100% mortality occurred. The optimal post-dew temperature for disease development was 18–25°C. Storage at <4°C maintained the infectivity of A. alternata strain 501 mycelia on E. adenophorum longer. Using light and scanning electron microscopy to examine the infection process of A. alternata Strain 501 mycelia, it was shown that the time from initiation to completion of infection with mycelia was much shorter (14 h) than with conidia (72 h). It was further shown that mycelial infection occurred predominately through direct penetration at intercellular junctions, while conidial infection occurred predominately through stomatal penetration. This suggests that mycelia are more suitable as infection propagules for A. alternata strain 501 in a bioherbicide for the control of E. adenophorum.     

Two cases of cutaneous phaeohyphomycosis by Alternaria alternata and Alternaria tenuissima

Two cases of cutaneous phaeohyphomycosis, one with a nodular appearance and the other with an erythematous infiltrating patch, are reported in immunocompromised patients. Diagnosis was based on histological examination, which revealed hyphae and round-shaped fungal cells in a granulomatous dermal infiltrate, and on identification of the moulds when biopsy fragments were cultured on Sabouraud-dextrose agar without cycloheximide. The pathogens were Alternaria tenuissima in the first case and A. alternata in the second. The fungi were examined by scanning electron microscopy. The patients were checked for bone and lung involvement and were then treated with surgical excision and itraconazole, and itraconazole only, respectively, with clinical and mycological resolution. This revised version was published online in August 2006 with corrections to the Cover Date.     

Effect of environmental factors on tenuazonic acid production by Alternaria alternata on soybean-based media

Aims: To determine the effects of water activity (a_W; 0·995–0·90), temperature (5, 18, 25 and 30°C), time of incubation (7–35 days) and their interactions on tenuazonic acid (TA) production on 2% soybean‐based agar by two Alternaria alternata strains isolated from soybean in Argentina. Methods and Results: TA production by two isolates of A. alternata was examined under interacting conditions of a_W, temperature and time of incubation on 2% soybean‐based agar. Maximum TA production was obtained for both strains at 0·98 a_W, but at 30 and 25°C for the strains for RC 21and RC 39, respectively. The toxin concentration varied considerably depending on a_W, temperature, incubation time and strain interactions. TA was produced over the temperature range from 5 to 30°C and a_W range from 0·92 to 0·995, however at 5 and 18°C little TA was produced at a_W below 0·94. Contour maps were developed from these data to identify areas where conditions indicate a significant risk for TA accumulation. Conclusions: The optimum and marginal conditions for TA production by A. alternata on soybean‐based agar were identified. The results indicated that TA production by A. alternata is favoured by different temperatures in different strains. Significance and Impact of the Study: Data obtained provide very useful information for predicting the possible risk factors for TA contamination of soybean as the a_W and temperature range used in this study simulate those occurring during grain ripening. The knowledge of TA production under marginal or sub‐optimal temperature and a_W conditions for growth are relevant as improper storage conditions accompanied by elevated temperature and moisture content in the grain can favour further mycotoxin production and lead to reduction in grain quality.     

L型氨基酸对烟草赤星病菌毒素毒性的影响

为确定不同氨基酸对烟草赤星病菌产生的毒素毒性的影响,作者采用摩擦接种处理法、浇根处理法、种子根处理法三种生物测定方法,确定了以烟草种子根处理法作为烟草赤星病菌的毒性测定方法。用12种氨基酸分别以5种不同浓度与AT毒素混合接种,根长测定结果表明：L-谷氨酰胺,L-天冬酰胺,L-组氨酸所有供试浓度均增强病原菌毒素的毒性,而其余9种L型氨基酸对烟草赤星病菌GL-6产生的毒素有抑制作用,其中L-甲硫氨酸、L-亮氨酸、L-赖氨酸适宜浓度可明显降低供试病原菌毒素对烟草的致病性,与对照差异极显著,其有效浓度分别为0．02mg／ml、0．02mg／ml、0．02～2mg／ml。     

链格孢Alternaria alternata侵染导致瓜类幼苗白化的机制

用分离自无症状瓜类植物的27株链格孢属Alternaria真菌接种黄瓜,有14株引起了黄瓜幼苗的白化,这些菌株均属于链格孢A. alternata。为揭示A. alternata引起黄瓜幼苗白化的机制,对代表菌株5F29经固体发酵后提取其次级代谢产物,将粗提物按一定量混入基质进行盆栽实验。结果表明,黄瓜、丝瓜和甜瓜对该粗提物敏感,出现白化苗;小白菜和辣椒对粗提物不敏感,生长正常。植物幼苗用粗提物处理的结果与用产生菌接种的结果相一致。粗提物经硅胶柱层析、葡聚糖凝胶柱层析及高效液相色谱（HPLC）等方法分离纯化得到一种活性化合物,经测定该化合物引起黄瓜幼苗白化的最低浓度为12.5μmol/L。该化合物在此浓度下可引起黄瓜幼苗生长点白化,在15μmol/L的浓度下可引起黄瓜幼苗大部分组织白化,致使幼苗很快死亡。应用核磁共振和质谱技术,确定了该化合物的结构,鉴定为一种植物毒素——腾毒素（tentoxin）。研究结果揭示了A. alternata引起瓜类幼苗白化的机制以及不同植物对于腾毒素的不同敏感性。     

Biotransformation of arenobufagin and cinobufotalin by Alternaria alternata

Abstract

The biotransformation of arenobufagin (1) and cinobufotalin (2), isolated from the natural medicine Chan Su, by Alternaria alternata AS 3.4578 was carried out. Incubation of 1 and 2 afforded six metabolites: 3-oxo-arenobufagin (1a), ψ-bufarenogin (1b), 3-oxo-ψ-bufarenogin (1c), 3-oxo-Δ⁴-derivative of cinobufotalin (2a), 3-oxo-cinobufotalin (2b) and 12β-hydroxycinobufotalin (2c). Among them, metabolites 1a, 1c and 2c are new compounds and their structures were characterized on the basis of their spectroscopic data (NMR, MS and IR). Compounds 1, 2, 1b, 2a and 2b were evaluated for their cytotoxicity against HepG2 and MCF-7 human cancer cells, and all of them showed significant inhibitory activities.     

Salicylic acid induced systemic resistant on peanut against Alternaria alternata

Abstract

The effect of Salicylic Acid (SA) in inducing resistance in groundnut plants against Alternaria alternata was investigated. Foliar application of SA at the concentration of 1 mM significantly reduced the leaf blight disease intensity and increased the pod yield under glasshouse conditions. Changes in the activities of phenylalanine ammonium lyase, chitinase β-1,3 glucanase and in phenolic content on groundnut after application of SA and inoculation with A. alternate were studied. In SA-treated leaves (plants) an increase in phenolic content was observed five days after challenge inoculation with A. alternata in groundnut plants pretreated with SA. There was a marked increase in chitinase and pathogen inoculation in SA-treated leaves. In chitinase, β-1,3 glucanase activities were observed in response to plants with an increase in SA treated leaves. Foliar applications of SA-induced in peroxidase and polyphenol oxidase activities were observed upon challenge inoculation with pathogen.     

β-Glucosidase from the cellulolytic system of Alternaria alternata autolyzed cultures

Abstract A β-glucosidase from centrifugated autolyzed cultures of Alternaria alternata has been purified 71 times by Sephadex G-200, CM-Biogel A and DEAE-Biogel A successively. The enzyme is a glycoprotein with 16% sugar and a M _r of 160 000, formed by two subunits of 60 000 and 80 000. The enzyme has optimum pH of 5 units and optimum reaction temperature of 50°C, being stable in a pH range of 3–8 and 0 to 60°C. The enzyme hydrolyzes different substrates showing maximum affinity and maximum hydrolysis velocity on cellobiose. The β-glucosidase is inhibited by gluconolactone but not by 10 mM glucose.     

Isolation and characterization of polymorphic microsatellite markers for Alternaria alternata

Alternaria alternata is of major significance as a food and feed contaminant and is able to produce a range of mycotoxins that may elicit adverse effects in both animals and humans. We describe the isolation and characterization of five microsatellite markers for studying A. alternata. Marker polymorphism was screened in 64 isolates of A. alternata. The number of alleles per locus ranged from eight to 24, and allelic diversity ranged from 0.425 to 0.882. These markers will be useful in the study of relationships and population genetics amongst isolates of A. alternata.