青藏高原有毒植物瑞香狼毒根抑菌活性初步研究

以人体病原细菌大肠杆菌、金黄色葡萄球菌、深部真菌白色念珠菌、浅部真菌红色毛癣菌、石膏样毛癣菌、石膏样小孢子菌、絮状表皮癣菌为供试菌,采用药敏纸片法对瑞香狼毒活性成分的抑菌活性进行了初步研究。结果表明瑞香狼毒对人体常见病原细菌和真菌有抑制作用,乙酸乙酯萃取物在33．33g／L浓度下对细菌组的抑菌圈直径最高可达12．02mm,对真菌组最高可达9．04mm,并初测瑞香狼毒中的抑菌活性物质主要为中偏强极性成分。     

瑞香狼毒根中活性物质的分离鉴定及作用机理

以瑞香狼毒根为研究材料,模式植物拟南芥为受体,采用实验室活体生物实验方法研究了瑞香狼毒根提取物及不同极性溶剂萃取物对7 d龄拟南芥幼苗的生长抑制作用;采用活性跟踪的化合物分离方法,分析了其中的活性化合物成分,并通过拟南芥DR5-GUS转基因株系,研究了单体化合物对拟南芥生长发育及根系生长素分布的影响.结果显示,瑞香狼毒根乙醇提取物对拟南芥有很强的生长抑制作用,其乙酸乙酯和氯仿萃取物的抑制活性最为显著,从氯仿萃取物中分离得到两种香豆素类化合物伞形花内酯(1)和西瑞香素(2),其中化合物1能够显著抑制拟南芥幼苗生长及根系发育,且明显降低了根部内源生长素的分布水平;化合物2也有较为明显的抑制活性.研究表明,氯仿和乙酸乙酯萃取物是瑞香狼毒植物毒活性的主要有效部位;伞形花内酯(1)和西瑞香素(2)是瑞香狼毒植物毒活性的有效成分,化合物1对拟南芥生长发育的抑制作用与生长素途径密切相关.     

成团泛菌低分子脂多糖的急性毒性、刺激性、致敏性及遗传毒性评估

本研究对成团泛菌低分子脂多糖(Pantoea agglomerans lipopolysaccharide,LPSp)的安全性进行初步评估.本研究采用一次限量法,用昆明种小鼠进行LPSp急性经口毒性试验,了解LPSp的急性毒性;采用新西兰兔分别进行LPSp急性和多次皮肤刺激性试验以及急性眼刺激性试验,了解LPSp的皮肤和粘膜刺激性;采用豚鼠进行LPSp皮肤变态反应试验,了解LPSp的致敏性;应用平板掺入法进行鼠伤寒沙门氏菌/回复突变试验和小鼠骨髓细胞微核试验考察LPSp的遗传危害.急性毒性试验结果显示,LPSp对小鼠经口一次灌胃的LD50大于5 000 mg/kg体重,属实际无毒级别;LPSp急性和多次皮肤刺激性试验以及急性眼刺激性试验结果显示,皮肤刺激和眼刺激积分均为0分,LPSp对皮肤无刺激性、对眼睛无急性刺激性;在皮肤变态反应试验中,LPSp在各观察时间点的皮肤变态反应积分均为0分,其致敏率均为0%,说明LPSp对豚鼠无致敏性; LPSp的鼠伤寒沙门氏菌/回复突变试验结果呈阴性(P>0.05);LPSp的小鼠骨髓细胞微核试验结果亦呈阴性,LPSp 各剂量组的微核发生率与阴性对照组未见统计学差异(P>0.05),而与阳性对照组有明显差异(P<0.01).本研究结果表明,在本实验剂量范围内,LPSp对小鼠经口毒性极低,属实际无毒级别,对家兔皮肤和眼睛无明显刺激性,对豚鼠无致敏性,对所试菌株和小鼠体细胞无诱变性和致突变性.     

紫茎泽兰醇提物的毒理学研究

为确保以紫茎泽兰提取物为主要原药的植物源农药的安全性,对紫茎泽兰醇提物进行了小鼠经口急性毒性试验、大白兔急性皮肤和眼刺激试验、小鼠骨髓嗜多染红细胞微核计数及小鼠精子畸形试验等急性毒性和遗传毒性试验。结果表明,受试物对两种性别的小鼠经口急性毒性试验,LD50大于5000mg／kg,对大白兔皮肤无刺激性;小鼠骨髓嗜多染红细胞微核试验及小鼠精子畸形试验结果均为阴牲,受试物未见遗传毒性。     

瑞香狼毒根的抑菌活性研究（Ⅰ）

以苹果干腐病菌、小麦赤霉病菌、番茄早疫病菌、南瓜枯萎病菌、玉米大斑病菌、烟草赤星病菌和辣椒疫霉病菌为供试菌,采用生物活性跟踪法、生长速率测定法和系统溶剂提取法对瑞香狼毒根中的杀菌活性物质进行了筛选和分离。结果表明,杀菌活性物质主要集中在乙酸乙酯提取物和甲醇粗提物中。从乙酸乙酯提取物中分离出两种杀菌活性物质AF1-4和AF1-5,同时还发现瑞香狼毒根中还存在增菌物质。     

噻吩磺隆的毒性及致突变性

选用大鼠、豚鼠及家兔,采用经口及皮肤,粘膜染毒途径,研究其急性毒性。同时有Ames试验,小鼠骨髓嗜多染红细胞微核试验及小鼠睾丸初级精母细胞染色体畸变试验进行致突变性研究,了解噻吩磺隆的毒性及致突变性。大鼠急性经口LD50大于5000mg／kg,经皮LD50大于2000mg／kg。家兔皮肤刺激试验阴性,轻度眼刺激性和弱致敏性。Ames试验,微核试验及小鼠睾丸初级精母细胞染色体畸变试验结果均为阴性。结论 噻吩磺隆属低毒性农药,在本实验条件下无致突变作用。     

瑞香狼毒根提取物对山楂叶螨的生物活性

采用不同的生物活性测定方法比较了瑞香狼毒(Stellera chamaejasme L.)根部4种不同溶剂提取物的杀螨活性。结果表明,瑞香狼毒根提取物对山楂叶螨(Tetranychus viennensis Zacher)有很好的触杀和内吸活性。在触杀活性测试中,石油醚提取物和氯仿提取物的杀螨活性最高;在内吸作用中,乙醇、氯仿和石油醚提取物的杀螨活性均较高,杀螨效果显著。在对石油醚提取物的不同溶剂萃取物进行生物活性追踪测定中发现,石油醚萃取物和氯仿萃取物具有较高的生物活性,浓度为0.6 g.L-1,山楂叶螨的24 h校正死亡率分别达到93.22%和79.66%。     

高通量测序分析甘肃高寒草原瑞香狼毒根内生菌群落结构特征研究

【背景】瑞香狼毒是我国天然草地退化的标志性植物之一,在入侵的过程中其根内微生物发挥着重要的作用,探究瑞香狼毒根内微生物群落对有益微生物资源的利用及生物防控瑞香狼毒具有重要意义。【目的】探究甘肃省祁连山东麓不同高寒草原毒性杂草瑞香狼毒根部内生真菌和细菌的组成、多样性等群落结构特征。【方法】通过Illumina MiSeq高通量测序技术对甘肃祁连山东麓不同高寒草原的瑞香狼毒根部内生菌组成及多样性进行分析。【结果】不同高寒草原瑞香狼毒根内子囊菌门(Ascomycota)在真菌中占优势地位;蓝细菌(Cyanobacteria)、变形菌门(Proteobacteria)、放线菌门(Actinobacteria)在根内生细菌中属于优势类群。G4样点的真菌和细菌OTU(OperationalTaxonomic Unit)数量和Shannon多样性指数均高于其他4个采样点。主坐标分析(Principal Coordinate Analysis,PCoA)表明,不同高寒草原瑞香狼毒根内生菌群落之间存在一定的差异。One-Way ANOVA分析结合Pearson相关性分析显示,不同样地瑞香狼毒真菌群落结构在属水平上相关性较小,而细菌在属水平存在一定的相关性。【结论】本研究为进一步开发利用瑞香狼毒内生真菌和细菌资源、阐明瑞香狼毒内生菌群的群落结构和生态功能提供理论参考。     

复合生物杀菌剂F6-11的安全性毒理学研究

目的：为研究复合生物杀菌剂F6．11毒性,采用动物实验法进行毒理学评价。方法：对复合生物杀菌剂F6-11进行小鼠急性毒性试验、小鼠骨髓嗜多染红细胞微核试验、亚急性毒性试验、家兔多次完整皮肤刺激试验、急性眼刺激试验、豚鼠皮肤变态反应试验、鱼类延长毒性14天试验。结果：复合生物杀菌剂F6—11对小鼠急性毒性LD50〉5000mg／kg．bw,属于实际无毒级物质;小鼠微核试验该杀菌剂各剂量组与阴性对照组比较,微核率无显著性差异（P〉0．05）;亚急性毒性试验动物血常规、生化指标及各脏器均未发现异常;对家兔多次完整皮肤及眼刺激反应积分均为0,均属无刺激性;对豚鼠皮肤变态反应试验组动物与阴性对照组无可见不同．试验组动物皮肤致敏反应积分为0,无致敏作用;鱼类延长毒性14天试验无异常。结论：毒理学研究表明,复合生物杀菌剂F6．11具有良好的使用安全性。     

白肉榕叶提取物的生物活性及化学成分研究

本文以白肉榕叶为研究对象,采用药剂浸泡法和平板涂布法分别测定了白肉榕乙醇粗提物对蚕豆蚜、致倦库蚊和福寿螺的毒杀活性以及对蜡样芽胞杆菌、大肠杆菌、伤寒杆菌、痢疾志贺氏菌和金黄色葡萄球菌5种供试菌的抑菌活性。结果表明,白肉榕乙醇粗提物对蚕豆蚜、致倦库蚊和福寿螺有生物活性,而对上述5种供试菌没有抑菌活性。采用液-液萃取法对白肉榕乙醇粗提物进行萃取分离,并对得到的石油醚萃取物、乙酸乙酯萃取物和水相3种不同极性部位进行生物活性测定。生物测定结果表明,白肉榕叶的活性成分主要存在于石油醚萃取物和乙酸乙酯萃取物中。从乙酸乙酯萃取物中进一步分离得到1个活性成分,经核磁共振氢谱(~1H NMR)和碳谱(~(13)C NMR)鉴定为桦木醇(betulin)。该化合物对致倦库蚊3龄幼虫具有较好的杀虫活性,24 h的LC50值为16.44 mg/L。     

侧柏乙醇提取物对21种植物病原真菌的抑菌活性

采用菌丝生长速率法测定了侧柏(Platycladus orientalis)叶、小枝、球果和种子4个不同部位乙醇提取物对21种植物病原真菌的抑菌活性。结果显示:(1)在供试浓度为50g/L(相当于干样)时,侧柏各部位乙醇提取物对4种供试植物病原真菌均具有较好抑制作用,其中侧柏叶提取物的抑菌效果最好,对供试葡萄白腐病菌(Conio-thyrium diplodiella)、葡萄黑痘病菌(Elsinoe ampelina)、番茄绵腐病菌(Phytophthora melongenae)和青霉病菌(Penicilliu mexpansum)的EC50分别为:5.424、3.186、8.913和19.000g/L。(2)侧柏叶乙醇提取物的石油醚萃取物和乙酸乙酯萃取物抑菌活性均较好,在供试浓度为0.5g/L时,石油醚萃取物对苹果腐烂病菌(Valsa mali)和葡萄黑痘病菌(E.ampelina)的抑菌率分别为80.35%和60.23%;乙酸乙酯萃取物对以上2种植物病原菌的抑菌率分别为81.88%和64.06%。结果表明:侧柏叶、小枝、球果和种子乙醇提取物均具有一定抑菌活性,叶乙醇提取物的活性最好,活性成分主要集中在石油醚萃取物和乙酸乙酯萃取物中。     

A protein from the mold Aspergillus giganteus is a potent inhibitor of fungal plant pathogens.

A purified preparation of antifungal protein (AFP) from Aspergillus giganteus exhibited potent antifungal activity against the phytopathogenic fungi Magnaporthe grisea and Fusarium moniliforme, as well as the oomycete pathogen Phytophthora infestans. Under conditions of total inhibition of fungal growth, no toxicity of AFP toward rice protoplasts was observed. Additionally, application of AFP on rice plants completely inhibited M. grisea growth. These results are discussed in relation to the potential of the afp gene to enhance crop protection against fungal pathogens in transgenic plants.     

ANTIFUNGAL ACTION OF STREPTOMYCIN-COPPER CHELATE AGAINST PHYTOPHTHORA INFESTANS ON TOMATO (LYCOPERSICON ESCULENTUM)

The antifungal protection afforded by streptomycin-copper chelate in vivo in greenhouse tests against Phytophthora infestans on tomato was found to be of the order of six times greater than that of streptomycin sulphate. The copper chelate also showed much greater resistance to simulated rainfall. Similar tests showed that streptomycin-copper chelate (in terms of streptomycin content) was from 2 1/2 to 5 times more effective as an antifungal prophylactic spray than zinc ethylene-bis(dithiocarbamate) (zineb), and some fifty times more active than copper oxychloride formulated as a commercial 50% wettable powder. These three materials showed roughly similar resistance to weathering by 'rainfall' and it was assumed therefore that 250 i.u./ml. streptomycin as streptomycin-copper chelate might be expected to give the same degree of protection against Phytophthora infestans in the field as would the usual field rates of usage of zineb and copper oxychloride.     

Antifungal activity of oosporein from an antagonistic fungus against Phytophthora infestans

An antifungal metabolite, oosporein, was isolated from the culture of Verticillium psalliotae that produced the antagonistic effects on Phytophthora infestans. Oosporein exhibited a significant growth-inhibitory effect on P. infestans in comparison with other phytopathogenic fungi.     

马铃薯晚疫病生防木霉菌的筛选及鉴定

采用马铃薯活体筛选法从268株木霉菌中筛选获得两株对致病疫霉有较强抑菌活性的木霉菌株R-5和T-15。这两株木霉菌代谢液可抑制病原菌生长及孢子囊萌发。温室防病试验发现,接种两株木霉菌可以减轻晚疫病的发生。田间试验进一步证明,两株木霉菌对晚疫病具有良好的田间防治效果,防效分别达到了72.4%和70.0%。经分子生物学方法鉴定,两株木霉菌分别为拟康氏木霉和棘孢木霉。实验构建的以活体筛选为基础的生防木霉菌筛选方法是一种可行高效的生防木霉菌筛选方式。     

Isarfelin, a peptide with antifungal and insecticidal activities from Isaria felina

Isarfelin, a peptide with inhibitory activity on mycelial growth in Rhizoctonia solani and Sclerotinia sclerotiorum and insecticidal activity toward Leucania separata, was isolated from the mycelia of Isaria felina. The IC₅₀ value of its antifungal activity against R. solani was 3.1 μg mL⁻¹. However, it was devoid of activity toward several bacterial species including Bacillus subtilis, E. coli and Staphylococcus aureus. The isolation procedure involved ethanol extraction, adsorption on YPR II macropore adsorption resin, ethyl acetate extraction, petroleum ether precipitation and recrystallization from ethyl acetate.     

Seed defensins of barnyard grass Echinochloa crusgalli (L.) Beauv

From the annual weed barnyard grass Echinochloa crusgalli (L.) Beauv., two novel defensins Ec-AMP-D1 and Ec-AMP-D2 that differ by a single amino acid substitution were isolated by a combination of different chromatographic procedures. Both defensins were active against several phytopathogenic fungi and the oomycete Phytophthora infestans at micromolar concentrations. The Ec-AMP-D1 showed higher activity against the oomycete than Ec-AMP-D2. The comparison of the amino acid sequences of the antifungal E. crusgalli defensins with those of earlier characterized T. kiharae defensins [T.I. Odintsova, Ts.A. Egorov, A.Kh. Musolyamov, M.S. Odintsova, V.A. Pukhalsky, E.V. Grishin, Seed defensins from T. kiharae and related species: genome localization of defensin-encoding genes, Biochimie, 89 (2007) 605-612.] that were devoid of substantial antifungal activity point to the C-terminal region of the molecule as the main determinant of the antifungal activity of E. crusgalli defensins.     

Pathogenesis-related PR-1 proteins are antifungal. Isolation and characterization of three 14-kilodalton proteins of tomato and of a basic PR-1 of tobacco with inhibitory activity against Phytophthora infestans.

Three distinct basic 14-kD proteins, P14a, P14b, and P14c, were isolated from tomato (Lycopersicon esculentum Mill. cv Baby) leaves infected with Phytophthora infestans. They exhibited antifungal activity against P. infestans both in vitro (inhibition of zoospore germination) and in vivo with a tomato leaf disc assay (decrease in infected leaf surface). Serological cross-reactions and amino acid sequence comparisons showed that the three proteins are members of the PR-1 group of pathogenesis-related (PR) proteins. P14a and P14b showed high similarity to a previously characterized P14, whereas P14c was found to be very similar to a putative basic-type PR-1 from tobacco predicted from isolated DNA clones. This protein, named PR-1 g, was purified from virus-infected tobacco (Nicotiana tabacum Samsun NN) leaves and characterized by amino acid microsequencing, along with the well-known acidic tobacco PR-1a, PR-1b, and PR-1c. The various tomato and tobacco PR-1 proteins were compared for their biological activity and found to display differential fungicidal activity against P. infestans in both the in vitro and in vivo assays, the most efficient being the newly characterized tomato P14c and tobacco PR-1g.     

Antibacterial and antifungal activities of andrachne cordifolia muell

The crude methanolic extract of Andrachne cordifolia Muell. (Euphorbiaceae) and its various fractions in different solvent systems (chloroform, ethyl acetate and n-butanol) were screened for antibacterial and antifungal activities. Crude extract and subsequent fractions demonstrated moderate to excellent antibacterial activities against the tested pathogens. Highest antibacterial activity was displayed by both chloroform and ethyl acetate fractions (100%) followed by the crude extract (68%) against Salmonella typhi. Similarly, crude extract and its subsequent fractions showed mild to excellent activities in antifungal bioassay with maximum (76%) antifungal activity against Microsporum canis by the chloroform fraction followed by the crude extract (65%).