五种新疆植物的抗真菌活性

对采自新疆的黄花蒿(Artemisia annua)、北艾(Artemisia vulgaris)、梭梭(Halaxylon ammodendron)、盐爪爪(Kalidium foliatum)和多枝柽柳(Tamarix ramosissima)抗植物病原真菌的活性进行了研究,植物病原真菌包括番茄灰霉病菌(Botrytis cinerea)、棉花枯萎病菌(Fusarium axysporum f.sp.vasinfectum)、稻瘟病菌(Magnaporthe grisea)、烟草黑胫病菌(Phytophthora parasitica var.nicotianae)和瓜果腐霉(Pythium aphani-dermatum),其中黄花蒿对真菌菌丝生长、多枝柽柳对稻瘟病菌孢子萌发表现出强的抑制活性。本研究为植物病害防治和新疆植物资源的开发和利用提供了依据。     

几种药用植物精油的抗真菌活性研究

研究了作用浓度为0：7-4．0μL/mL的南方药用植物香茅（Cymbopogon citratus）、广藿香（Pogostemon cablin（Blanco）Benth）、大叶桉（Eucalyptus robusta Smith）和蛇床（Cnidium monnier（L.）Cusson）的精油对6种植物病原真菌的抑制活性。结果表明,大叶桉、广藿香和香茅精油对串珠镰刀病菌（Fussarium moniliforme）、玉米弯孢霉菌（Curvjlaria lunata）对多种供试植物病原真菌的生长有明显抑制活性,其中,香茅精油在浓度为3．3μL/mL时,能完全抑制大部分供试真菌的生长。但不同精油对于各病原真菌的抑制率有一定差异。本研究为复合植物精油抗真菌农药的开发提供依据。     

菊状千里光化学成分及抗真菌活性研究

研究菊状千里光的化学成分,为进一步探讨其药理作用提供理论依据.菊状千里光乙醇提取物经大孔树脂初步分离后,采用凝胶色谱、硅胶色谱、MCI等方法分离纯化化合物,通过化合物的理化性质与波谱数据分析鉴定其结构.使用MTT法测定分离得到的两个生物碱对正常肝细胞L-02的毒性,并通过琼脂平板打孔法对菊状千里光中得到的部分化合物进行...     

三种药用植物内生真菌抗真菌活性的研究

从雪上一枝蒿(Aconitumbrachypodum)、刺五加(Acanthopanaxsenticosus)和大血藤(Sargentodoxacuneata)分离获得的162株内生真菌进行抗真菌活性检测,结果具有抗菌活性菌株有74株,雪上一枝蒿15株,刺五加23株,大血藤36株,分别占3种植物各自内生真菌的44.12%,48.94%和44.44%。将具有抗菌活性的菌株进行分类鉴定,分属于6目、7科、23属。     

小桐子内生真菌及其抗真菌活性研究

从药用植物小桐子的根和茎中分离到内生真菌57株,经鉴定,它们分属于15个不同的分类单元。其中拟盘多毛孢为优势属,其次为拟茎点霉属和茎点霉属。用杨桃炭疽菌,香蕉疫霉和镰刀菌作指示菌对这些内生真菌的抗真菌活性进行检测,结果表明,有2株菌对杨桃炭疽菌具有抑菌活性。     

马铃薯糖苷生物碱对人血胆碱酯酶的抑制

马铃薯糖苷生物碱是一类有异味有毒性的含氨甾族化合物,其致毒机理与有机磷杀虫剂相似,表现出对人体内胆碱酯酶活性的抑制,使胆碱能神经兴奋增强,引起一系列中毒症状。从块茎萌发芽中提取的总糖苷生物碱的毒性较高,对人血胆碱酯酶的体外抑制率为６３．０８％,单个糖苷生物碱（α茄碱和α卡茄碱）的毒性较低,抑制率分别为５２．０８％和４１．１５％,总糖苷生物碱的水解产物糖苷配基基本无毒性,抑制率仅为１１．３６％。     

海洋微生物几丁质酶分离纯化及其抗真菌活性

以实验室筛选的海洋产几丁质酶短芽胞杆菌属（Bacillus brevis sp．）菌株Bspl,经往复式摇床振荡培养96h后,发酵液先后采取了75％的硫酸铵盐析、透析、几丁质亲和层析、SDS—PAGE等方法对几丁质粗酶液进行分离纯化和鉴定。几丁质亲和层析一步纯化后,经过SDS—PAGE电泳测定该酶的分子量为23ku,其比活力为86．65．纯化倍数为1．707、产率为32．1％。纯化的几丁质酶能抑制病原真菌的生长,对病原真菌的拮抗作用具有广谱性。同时研究了几丁质酶的稳定性,以胶态几丁质为底物,分离的几丁质酶在pH7．5,55．0℃左右具有最大酶活性;Zn^2＋、Cu^2＋和Hg^2＋能强烈抑制几丁质酶活性;Ni^＋和EDTA抑制20％-40％;然而5mmol／LCo^2＋可以使几丁质酶活性提高1．4倍;Mg^2＋、Ca^2＋等也能使酶活性增加。     

中药提取物对酵母菌抗真菌活性研究

目的探讨6味中药2种方法提取成分对酵母菌的抑菌和杀菌作用。方法采用药基琼脂稀释法,测定6味中药水提和醇提成分对白念珠菌和糠秕马拉色菌的MIC和MFC。结果对白念珠菌：水提黄连、醇提黄柏、醇提土槿皮MIC范围分别为0．625—1．25mg／mL、0．625～1．25mg/mL、0．313—0．625mg／mL;均值均为0．625mg／mL;对糠秕马拉色菌：水提和醇提黄连MIC范围分别为0．625～1．25mg／mL和1．25mg／mL,均值均为1．25mg／mL。对白念珠菌：醇提土槿皮MFC范围0．625～2．5mg/mL,均值0．625rag／mL。结论水提黄连、醇提黄柏和土槿皮对白念珠菌有较强抑菌作用,其中醇提土槿皮有较强杀菌作用。水提和醇提黄连对糠秕马拉色菌有较强抑菌作用。     

家蝇幼虫血淋巴中抗真菌肽的诱导方法比较及抗真菌活性

以未诱导组作为空白对照研究比较真菌诱导、超声诱导和热诱导家蝇Musca domestica 幼虫血淋巴初提液的抗真菌肽效果,比较各种诱导方法诱导后的幼虫存活率;用凝胶层析法和高效液相分离纯化热诱导家蝇3龄幼虫抗真菌肽,检测其抗白假丝酵母菌Candida albicans和新生隐球菌Cryptococcus neoformans活性;SDS-PAGE分析抗真菌肽的蛋白分子量范围。结果表明：3种诱导方法诱导后家蝇幼虫均产生具有明显抗真菌作用的抗真菌肽,其初提液抑菌圈大小没有明显差别;真菌诱导组和热诱导组幼虫存活率低于对照组,而超声诱导组与对照组相比则无明显差别。经分离纯化后,抗真菌肽仍具有较好的抗真菌活性;SDS-PAGE分析表明该抗真菌肽有效成分的蛋白分子量在14.4 kD以下。结果提示热诱导家蝇幼虫产生抗真菌肽是一种方便、有效的诱导方式。     

黑腹果蝇抗真菌肽Drosomycin同系物的免疫原性和抗真菌活性

通过黑腹果蝇 Drosophila melanogaster抗真菌肽Drosomycin（Drs）及其同系物Drs-lC和Drs-lE的抗体制备及Western blotting 结果,分析了Drs同系物的免疫原性与其抗真菌活性的关系。研究采用了2种技术路线,分别将Drs、Drs-lC和Drs-lE 基因构建成与细胞生长因子基因 afgf 融合的重组表达质粒 pET-afgf-Drs、pET-afgf-C和pET-afgf-E,以及通过基因同向串连获得重组表达质粒 pRSET-2Drs、4Drs、6Drs 和 pRSET-2E、4E、6E,并将这些重组表达质粒转化到BL21（DE3）plysS受体菌进行诱导表达。分离纯化后的融合蛋白afgf-Drs、afgf-C和afgf-E 以及串连蛋白 4 Drs、4 Drs-lE分别免疫小白鼠获得相应的抗血清。Western blotting免疫原性检测结果表明,Drs及其同系物与各自的抗血清具有强的免疫反应,同时相互间也有交叉免疫反应,提示它们具有相似的主要抗原决定簇,这些抗原决定簇可能与抗真菌活性无关。同系物之间抗真菌活性的差异可能来源于某些细微结构上的差异。     

Antifungal Activity of Volatile Compounds Produced by an Edible Mushroom Hypsizygus marmoreus against Phytopathogenic Fungi

Volatile compounds with antifungal activity produced by edible mushrooms have potential as biological control agents to combat fungal diseases and reduce fungicide use in agriculture. Here we investigated the antifungal activity of volatile compounds produced by the edible mushroom Hypsizygus marmoreus (TUFC 11906) against eight phytopathogenic fungi. The results showed that volatile compounds from the mycelia and culture filtrates (CFs) of H. marmoreus had antifungal activity against some phytopathogenic fungi. Among them, the mycelial growth and conidial germination of Alternaria brassicicola were significantly inhibited by 60 and 100%, respectively. Moreover, the volatile compounds from CFs inhibited the lesion formation of A. brassicicola on detached cabbage leaves by 94%. The volatile compounds had higher antifungal activity against A. brassicicola than other fungi. With the removal of the volatile compounds from conidia of A. brassicicola, the conidia began to germinate, which indicates fungistatic activity of the compounds. The volatile compounds were isolated from the CFs of H. marmoreus, and the major volatile compound with antifungal activity was estimated to be 2‐methylpropanoic acid 2,2‐dimethyl‐1‐(2‐hydroxy‐1‐methylethyl)propyl ester. As the volatile compound produced by H. marmoreus is a product of an edible mushroom and has fungistatic activity against some phytopathogenic fungi, especially A. brassicicola, it may be possible to use the compounds as a novel safe agent for protecting crops in the field and during storage.     

杜仲内生真菌的多样性分析及其抗植物病原真菌的活性

以河南郑州和江苏徐州采集到的杜仲为材料,采用纯培养方法对杜仲内生真菌进行分离。将分离纯化得到的90株真菌通过形态学鉴定并进行多样性分析,90株内生真菌分别属于13个属,其中茎点霉属(Phoma)和链格孢属(Alternaria)为优势菌群,分别占总菌株数的18%和16%;其次为黑孢属(Nigrospora)和枝孢属(Cladosporium),均占总菌株数的10%。用平板对峙法对分离得到的杜仲内生真菌进行抗植物病原真菌实验,发现有18个菌株对至少一种病原真菌具有明显的拮抗作用。通过比色法进行内生真菌产IAA(吲哚乙酸)定性实验,结果显示,有37株真菌具有产IAA能力,通过分光光度法对这37株真菌进行产IAA定量实验,发现有8株有较好的产IAA活性。     

Antifungal Activity of Cadinane-Type Sesquiterpenes from Eupatorium adenophorum against Wood-Decaying Fungi

The present study aimed to evaluate the antifungal activities of Eupatorium adenophorum against four strains of wood-decaying fungi, including Inonotus hispida, Inonotus obliquus, and Inonotus cuticularis. Bioguided isolation of the methanol extract of E. adenophorum by silica gel column chromatography and high-performance liquid chromatography afforded six cadinane-type sesquiterpenes. Their structures were identified by nuclear magnetic resonance and MS analyses. According to the antifungal results, the inhibition rate of the compound was between 59.85 % and 77.98 % at a concentration of 200 μg/mL. The EC₅₀ values ranged from 74.5 to 187.4 μg/mL.     

Synergistic Mixtures of Fungitoxic Monochloro and Dichloro-8-Quinolinols against Five Fungi

Fourteen mono- and dichloro-8-quinolinols were tested against five fungi (Aspergillus niger, A. oryzae, Myrothecium verrucaria, Trichoderma viride, and Mucor circinelloides) and compared with the fungitoxicity of 8-quinolinol in Yeast Nitrogen Base containing 1% D-glucose and 0.088% L-asparagine. All of the compounds were more fungitoxic than 8-quinolinol except for the surprising activity of 8-quinolinol against A. oryzae. Mixtures of the MICs of monochloro- and dichloro-8-quinolinols in which the halogens were in different positions of the quinoline ring showed synergism. Comparable mixtures in which one position of each compound was occupied by the same halogen showed additive activity. In a different study we showed that 3,5,6-, 3,5,7-, 4,5,7-, and 5,6,7-trichloro-8-quinolinols were not toxic to M. circinelloides, whereas the combinations of the correspondingly substituted mono- and dichloro-8-quinolinols as well as 3,6-dichloro- and 5,7-dichloro-8-quinolinols were inhibitory. This indicated that a steric factor can be involved in affecting fungitoxicity.     

Large-Scale Screening of the Plant Extracts for Antifungal Activity against the Plant Pathogenic Fungi

Plants produce chemicals of immense diversity that provide great opportunities for development of new antifungal compounds. In search for environment-friendly alternatives to the fungicide of current use, we screened plant extracts obtained from more than eight hundred plant materials collected in Korea for their antifungal activity against the model plant pathogenic fungus, Magnaporthe oryzae. This initial screening identified antifungal activities from the eleven plant extract samples, among which nine showed reproducibility in the follow-up screening. These nine samples were able to suppress not only M. oryzae but also other fungal pathogens. Interestingly, the plant extracts obtained from Actinostemma lobatum comprised five out of eight samples, and were the most effective in their antifungal activity. We found that butanol fraction of the A. lobatum extract is the most potent. Identification and characterization of antifungal substances in the A. lobatum extracts would provide the promising lead compounds for new fungicide.     

A Novel Isoindoline,Porritoxin Sulfonic Acid,from Alternaria porri and the Structure-phytotoxicity Correlation of Its Related Compounds

Novel zinniol-related compound 3, named porritoxin sulfonic acid, with an isoindoline skeleton was isolated from the culture liquid of Alternaria porri. The structure was determined to be 2-(2″-sulfoethyl)-4-methoxy-5-methyl-6-(3′-methyl-2′-butenyloxy)-2,3-dihydro-1H-isoindol-1-one. The phytotoxic activities of three isoindolines (1-3) were evaluated in a seedling-growth assay against stone leek and lettuce.     

The Chitinolytic Activity of Bacillus Cohn Bacteria Antagonistic to Phytopathogenic Fungi

Among the 70 tested Bacillus spp. strains antagonistic to phytopathogenic fungi, 19 were found to possess chitinolytic activity when grown on solid media with 0.5% colloidal chitin. The chitinolytic activity of almost all of these 19 strains grown in liquid cultures ranged from 0.1 to 0.3 U/ml. One of the 19 strains exhibited exochitinase activity. In addition to chitinase, two strains also produced chitosanase and one strain, -1,3-glucanase. No correlation was found between the antifungal activity of the bacillar strains studied and their ability to synthesize extracellular chitinase. Among the 19 chitinolytic strains, the correlation between these parameters was also low (r _{x , y} = 0.45), although the enzymatic preparations of most of these strains inhibited the growth of the phytopathogenic fungus Helminthosporium sativum.