期刊文献+

新型杀菌剂苯并咪唑喹啉铜对辣椒疫霉的抑菌活性 被引量:3

Effective of Carbendazim-oxine-copper,a novel fungicide against Phytophthora capsici
原文传递
导出
摘要 [目的]苯并咪唑喹啉铜是多菌灵和喹啉铜螯合而成的新杀菌剂。为明确其应用价值,测定了它对辣椒疫霉的抑菌效果。[方法]分别用生物测定法和盆栽法测定了药剂对辣椒疫霉各发育阶段的离体活性以及活体药效。[结果]苯并咪唑喹啉铜对游动孢子囊形成、萌发以及游动孢子休止孢萌发均有很好的抑制效果,EC50值在0.01~0.2 mg/L之间;活体试验中,200 mg/L苯并咪唑喹啉铜防效达73.46%。[结论]该药剂还具有兼治多种真菌病害的潜力,对合成新农药和治理抗药性风险具有很大价值。 Carbendazim-oxine-copper is a novel chelate of carbendazim and oxine-copper.To clarify its possibility of application,inhibition against Phytophthora capsici Leonian was tested.[Methods]We used bioassay method to identify the inhibitory effect of P.capsici in different development stages in vitro and potted pepper to evaluate the efficacy of carbendazim-oxine-copper in vivo respectively.[Results]Test results in vitro indicated that Carbendazim-oxine-copper had excellent inhibitory effect against sporangium formation,sporangium germination,and zoospore cyst germination of P.capsici,with EC50 values of 0.01-0.2 mg/L.Besides,carbendazim-oxine-copper at 200 mg/L provided 73.46% protective control efficacy against P.capsici in vivo.[Conclusions]carbendazim-oxine-copper has enormous potential to control a variety of fungal diseases,and therefore has great value to be exploited for the synthesis of new fungicides and resistance management.
出处 《农药》 CAS 北大核心 2011年第8期602-605,共4页 Agrochemicals
关键词 杀菌剂 苯并咪唑喹啉铜 辣椒疫霉 抑菌 抗药性 fungicide crbendazim-oxine-copper Phytophthora capsici inhibition resistance
  • 相关文献

参考文献12

二级参考文献75

共引文献80

同被引文献32

  • 1汪泉,张大永,吴晓明.植物源大环二萜类化合物生物活性的研究进展[J].中国药科大学学报,2009,40(5):474-480. 被引量:3
  • 2司美茹,薛泉宏,余博,袁虎林,陈占全.辣椒疫霉生防菌的双重筛选[J].植物保护学报,2006,33(1):41-46. 被引量:30
  • 3XU Jun-guang, ZHAO Xiao-ming, HAN Xiu-wen. Antifungal Activity of Oligochitosan against Phytophthora capsici and Other Plant Pathogenic Fungi in vitro [J]. Pesticide Biochemistry and Physiology, 2007, 87: 220-228.
  • 4Gil-Jae Joo. Production of an Anti-fungal Substance for Biological Control of Phytophthora capsici Causing Phytophthora Blight in Red-peppers by Streptomyces halstedii[J]. Biotechnology Letters, 2005, 27: 201-205.
  • 5LAMOUR K H, HAUSBECK M K. Mefenoxam Insensitivity and the Sexual Stage of Phytophthora eapsici in Michigan Cucurbit Fields[J]. Phytopathology, 2000: 396-400.
  • 6DESHPANDE B S, AMBEDKAR S S, SHEWALE J G. Biologically Active Secondary Metabolites from Streptomyces[J]. Enzyme and Microbial Technology, 1988, 10(8): 455-473.
  • 7MOTOHASHI K, UENO R, SUE M. Studies on Terpenoids Produced by Actinomycetes: Oxaloterpins A, B, C, D and E, Diterpenes from Streptom?ves sp. KO-3988[J]. Journal of Natural Products, 2007, 70(11): 1712-1717.
  • 8XIE Peng-fei, MA Ming, RATEDB M E. Biosynthetic Potential-Based Strain Prioritization for Natural Product Discovery: A Showcase for Diterpenoid-producing Actinomycetes[J]. Journal of Natural Products, 2014, 77: 377-387.
  • 9MOTOHASHI K, IRIE K, TODAY. Studies on Terpenoids Produced by Actinomycetes [J]. Japan Antibiotics Research Association, 2008, 61(2): 75-80.
  • 10OVERVOORD P, FUKAKI H, BEECKMAN T. Auxin control of root development [ J]. Cold Spring Harb Perspect Biol, 2010, 2 (6): 1-16.

引证文献3

二级引证文献14

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部