一株产胶霉菌素菌株的ARTP诱变及筛选

试验旨在选育出胶霉菌素高产菌株,以胶霉菌素产生菌TY-009为初始菌株,利用常压室温等离子体(ARTP)诱变技术对产胶霉菌素的绿色木霉菌株进行诱变处理,并设置时间梯度,检测不同处理时间样品的胶霉菌素产量。通过平板筛选以及摇瓶复筛选出8株正突变菌株,其中产率最高达到0.86 mg/m L,较初始菌株的产率提高了45.76%。ARTP诱变方法快速、高效,对绿色木霉菌株的诱变效果良好,在提高胶霉菌素产量方面有很好的应用前景。     

生物刺激素协同对草莓炭疽病防治及其生长发育的影响

草莓炭疽病是草莓定植时期最易造成死苗的真菌病害。本文研究了生物刺激素（木霉菌、海藻酸、聚谷氨酸）协同灌根对草莓炭疽病的防治以及促生作用。结果表明,与对照相比,木霉菌、海藻酸、聚谷氨酸单剂灌根和木霉菌+海藻酸、木霉菌+聚谷氨酸的协同灌根处理均能显著降低炭疽病造成的死苗率,其中木霉菌+海藻酸的防效最高,可达78.26%。相比对照,所有处理均能显著提高净光合速率、1,5-二磷酸核酮糖羧化酶活性和加氧酶活性等光合指标,以及土壤脲酶活性。协同灌根处理显著提高草莓株高、根茎粗、叶柄长、叶面积等生长指标达15.62%～47.00%。其中木霉菌+海藻酸处理的净光合速率、土壤脲酶活性最高。综合而言,木霉菌与海藻酸协同灌根在促进生长、促进光合、提高土壤供氮水平以及防控草莓炭疽病方面均表现出显著的增效作用,可作为生物防治的一种有效手段     

木霉菌对苹果主要真菌病害的抑制及其在土壤中的定殖作用

以胶东半岛老的果园中土壤为试材,采用逐步稀释法,涂平板于孟加拉红培养基中,根据形态和分子方法鉴定分离木霉菌。分离出的木霉菌与苹果主要病害对峙培养在不同pH的培养基上,观察不同pH条件下,对真菌病害的抑制效果。土壤有机质和pH是目前胶东果园的主要问题,采用正交法设计,研究了不同的土壤条件对木霉菌生长的影响。结果表明:在不同pH条件下,木霉菌抑制苹果病原真菌的效果不同,木霉菌在不同的pH条件下对腐烂病(Valsa mali)和炭疽病(Colletotrichum gloeosporioides)均可以抑制,但对轮纹病(Physalospora piricola Nose)只有在pH 6.0时没有效果外,其它pH时都对轮纹病有抑制作用。在土壤pH 6.5和土壤有机质含量为75 g·kg^-1时,最有利于木霉菌定殖。同时还发现木霉菌对土壤的pH具有调节作用,无论在碱性条件下,还是酸性条件下,均可以使土壤pH趋于中性,另外木霉菌可以增加土壤有机质含量,特别是在高土壤有机质含量的情况下,增加更加显著。总之,分离出的木霉菌对苹果腐烂病、炭疽病和轮纹病抑制效果好。土壤pH和有机质含量对木霉菌的生长有影响,高土壤有机质含量和中性土壤有利于木霉菌定殖。另外,木霉菌能有效地改良土壤有机质含量和土壤pH。     

紫外光诱导哈茨木霉产生对多菌灵抗药性的菌株

在含多菌灵药物培养基上，采用紫外光重复诱导处理的方法，对拮抗性哈茨木霉T24进行改良，选育出对多菌灵具有显著耐药性的菌株T24—4和T24—6。结果表明，多菌灵浓度为300mg·L^-1时，对突变菌株T24—4和T24—6的抑制率分别为9．4％和3．0％。同时两菌株对速克灵和甲基托布津也有交互抗性。经过菌和药协同作用研究发现：木霉菌T24—6菌剂与多菌灵重量配比为8：2时，协同抑菌率高达85．0％，明显高于分别单独使用T24—6和多菌灵的抑菌率（70．3％和69．6％）。分别用菌和药，药，菌1000倍稀释液进行草莓活体拮抗性测定，其对草莓灰霉病的防治效果分别为83．9％、67．9％和64．2％，进一步表明菌和药协同作用效果优势更明显。在使用木霉T24—6菌剂防治农作物病害时，添加少量的多菌灵，可降低植物病原菌的活性和侵染力，从而提高生防效果。     

Effect of biocontrol agents and biofertilizers on root rot,yield, harvest index and nutrient uptake of cassava (Manihot esculanta Crantz)

Cassava is an important subsidiary food and industrial raw material in the tropics. Root rot disease, caused by Phytophthora palmivora, poses a serious threat to cassava cultivation in Tamil Nadu, India. Field experiments (2008–09) were conducted to study the effect of biocontrol agents (Trichoderma spp. and Pseudomonas fluorescens) and biofertilizers (Azospirillum, vesicular–arbuscular mycorrhizal fungi and phosphorus-solubilizing bacteria) on root rot, yield, harvest index and nutrient uptake of cassava at two NPK rates. The design of the experiment was a split plot with two NPK rates, recommended and 50% recommended rate, as the main plot treatments and five biocontrol agents and biofertilizers as subplot treatments. The results clearly indicated that use of a bioinoculants consortium significantly reduced root rot infection/disease incidence over uninoculated controls. Azospirillum significantly improved the yield of cassava at 50% of the recommended rate of NPK. NPK rates had no significant impact on harvest index of cassava and Trichoderma and vesicular–arbuscular mycorrhizal fungi resulted in a higher harvest index even at 50% of the recommended NPK rate. Nitrogen, phosphorus and potassium uptake was significantly improved when treated with biofertilizers and/or a consortium.     

Effectiveness of Coniothyrium minitans and Trichoderma atroviride in suppression of sclerotinia blossom blight of alfalfa

The effects of the mycoparasites Coniothyrium minitans and Trichoderma atroviride on the suppression of alfalfa blossom blight caused by Sclerotinia sclerotiorum were evaluated under indoor and field conditions. When T. atroviride (9·0 × 10⁴ conidia/floret) + S. sclerotiorum (6·0 × 10³ ascospores/floret) or C. minitans (9·0 × 10⁴ conidia/floret) + S. sclerotiorum (6·0 × 10³ ascospores/floret) were applied to detached young alfalfa florets, T. atroviride effectively inhibited saprophytic growth of S. sclerotiorum, whereas C. minitans showed no inhibition under the same conditions. When T. atroviride (6·9 × 10⁴ conidia/floret) + S. sclerotiorum (6·0 × 10³ ascospores/floret) or C. minitans (6·9 × 10⁴ conidia/floret) + S. sclerotiorum (6·0 × 10³ ascospores/floret) was applied to young alfalfa petals in vivo just after pollination, the percentage of pod formation was higher for T. atroviride+S. sclerotiorum than that for C. minitans+S. sclerotiorum, and the percentage of pod rot was lower for T. atroviride+S. sclerotiorum than that for C. minitans+S. sclerotiorum. However, when they were applied to senescent petals attached to developing pods of alfalfa at 9·2 × 10⁴ conidia/floret together with S. sclerotiorum at 4·5 × 10³ ascospores/floret at 14 days after pollination, C. minitans was more effective than T. atroviride in suppressing sclerotinia pod rot and seed rot of alfalfa. Field experiments showed that three applications of C. minitans (5·4 × 10⁶ conidia mL⁻¹) or T. atroviride (5·4 × 10⁶ conidia mL⁻¹) at a 7-day interval to blossoms of alfalfa effectively suppressed sclerotinia pod rot in two out of three annual trials. Coniothyrium minitans effectively suppressed sclerotinia seed rot in all three years, whereas T. atroviride was not effective against seed rot in any of the trial years. The efficacy of C. minitans was not significantly different (P > 0·05) from benomyl (250 µg ai mL⁻¹). This study suggests that C. minitans has potential as a biocontrol agent to control blossom blight of alfalfa caused by S. sclerotiorum.     

The process of antagonism of Sclerotium cepivorum in white rot affected onion roots by Trichoderma koningii

Trichoderma koningii (strain Tr5) grew in the epidermal mucilage of onion roots without entering healthy epidermal tissue. When placed on the epidermis of Sclerotium cepivorum -infected roots, T. koningii colonized epidermal passage cells, with little colonization of other epidermal tissues, then branched and spread throughout the root cortical tissues damaged by enzymes and toxins which diffused ahead of S. cepivorum hyphae, and impeded the path of the infection. When T. koningii colonized infected tissue, many S. cepivorum hyphae became detached at septa, cell walls dissolved and many hyphal apices burst. Contact between hyphae was not necessary for lysis to occur. T. koningii produced two endochitinases ( R _f 0·15 and 0·24) and two exo-acting chitinolytic enzymes ( R _f 0·46 and 0·62) during degradation of crabshell chitin and S. cepivorum cell walls. The R f 0·24 and 0·46 proteins were detected when T. koningii colonized S. cepivorum -infected roots and are likely to be a component of the antagonism process.     

Evaluation of Microbial Antagonists for Biological Control of Botrytis cinerea Stem Infection in Cucumber and Tomato

Of fifteen isolates of yeasts, filamentous fungi and bacteria and a commercial product, tested in a bioassay with stem segments, eleven isolates consistently reduced incidence of disease and sporulation of Botrytis cinerea Pers; Fr in tomato and seven isolates in cucumber. Several isolates reduced disease by more than 75% in all experiments. Six antagonists that performed well in the bioassays and that were fairly easy to produce in vitro, were selected for further testing in two glasshouse experiments with cucumbers. After application of spores of B. cinerea and the antagonists or the fungicide tolylfluanid to pruning wounds, disease incidence was reduced by 50–100% by all antagonists in both experiments and only in one experiment by tolylfluanid.For Trichoderma harzianum T39, Aureobasidium pullulans and Cryptococcus albidus, biological control efficacy in bioassays with cucumber stem segments was not strongly influenced by temperatures in the range between 18 and 30°C, but at 24°C the efficacy of the three antagonists strongly decreased at relative humidities of 90% and 80% (vapour pressure deficits 0.299 and 0.598kPa, respectively) compared to 100.     

The potential of nonpathogenic Fusarium oxysporum and other biological control organisms for suppressing fusarium wilt of banana

The aim of this study was to evaluate the ability of nonpathogenic F. oxysporum and Trichoderma isolates from suppressive soils in South Africa to suppress fusarium wilt of banana in the glasshouse. Several biological control agents and commercial biological control products were included in the study. The isolates were first screened in vitro on potato dextrose agar. In glasshouse evaluations, the fungal and bacterial isolates were established on banana roots before they were replanted in pathogen-infested soil, while the commercial biocontrol agents were applied as directed by the supplier. Banana plantlets were evaluated for disease development after 7 weeks. In vitro tests showed none of the nonpathogenic isolates suppressed Fusarium oxysporum f.sp. cubense ( Foc ), while slight suppression was observed with the two Trichoderma isolates. Results of the glasshouse evaluations revealed that two of the nonpathogenic F. oxysporum isolates, CAV 255 and CAV 241, reduced fusarium wilt incidence by 87·4 and 75·0%, respectively. The known biological control agent Fo47 did not suppress Foc significantly. Pseudomonas fluorescens strain WCS 417, known for its ability to suppress other fusarium wilt diseases (WCS 417), reduced disease incidence by 87·4%. These isolates should be further evaluated for potential application in the field, independently and in combination.     

3株木霉(Trichoderma spp.)对华山松疱锈病菌锈孢子的破坏作用

从不同来源的茶藨生柱锈锈孢子堆和疱锈病枝干上分离获得3株木霉,室内生测结果表明,3株木霉的菌丝和培养滤液对锈孢子壁有较强的破坏作用;菌株TR2和TR3在锈孢子堆上生长速度快,锈孢子死亡率随孢子壁破坏率的增加而升高,锈孢子壁对孢壁降解酶有强烈诱导作用;TR1对锈孢子壁的破坏作用弱于TR2和TR3,但在PD培养液中有较强的产毒能力,锈孢子壁能抑制TR1菌株产毒。