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利用Brevibacillus laterosporus YMF3.00003菌株研制生物杀菌剂
引用本文:周峻沛,顾英琦,陈昱君,李世东,莫明和,张克勤.利用Brevibacillus laterosporus YMF3.00003菌株研制生物杀菌剂[J].云南大学学报(自然科学版),2006,28(5):456-460.
作者姓名:周峻沛  顾英琦  陈昱君  李世东  莫明和  张克勤
作者单位:1. 云南大学,省部共建生物资源保护与利用重点实验室培育基地,云南,昆明,650091
2. 云南省文山州三七研究所,云南,文山,663000
3. 中国农业科学院,生物防治研究所,北京,100081
基金项目:云南省省院省校合作项目(2001ZCBFB01L053)
摘    要: Brevibacillus laterosporus YMF3.00003菌株具有广谱抗真菌活性,摇瓶培养发酵液对所测的植物病原菌Cylindrocarpon didynum,C.destructans,Magnaporthe grisea,Rhizoctonia solani的菌丝生长有较强的抑制作用,最强抑制率分别为81.5%,71.0%,60.7%和60.2%.确定了该菌株在20 L发酵罐中的发酵条件,绘制了生长曲线及得到了不同生长时期的抑菌率.其中,培养21 h时细胞数最多,达到5.1×109;25 h时发酵物对R.solani的抑菌率最高,达到90.5%.通过对几种吸附剂的筛选,确定用锯木屑作为吸附剂,将发酵终产物用锯木屑吸附,制成约2×1011g-1的菌剂.

关 键 词:Brevibacillus  laterosporus  生物菌剂  植物病原菌  发酵
文章编号:0258-7971(2006)05-0456-05
修稿时间:2006年3月15日

Development of a formulation against phytopathogens using Brevibacillus laterosporus YMF3. 00003 strain
ZHOU Jun-pei,GU Ying-qi,CHEN Yu-jun,LI Shi-dong,MO Ming-he,ZHANG Ke-qing.Development of a formulation against phytopathogens using Brevibacillus laterosporus YMF3. 00003 strain[J].Journal of Yunnan University(Natural Sciences),2006,28(5):456-460.
Authors:ZHOU Jun-pei  GU Ying-qi  CHEN Yu-jun  LI Shi-dong  MO Ming-he  ZHANG Ke-qing
Institution:1. Laboratory for Conservation and Utilization of Bio-resources, Yunnan University, Kunming 650091, China;2. Wenshan Prefectural P.notogingseng Research Institute of Yunnan Province, Wenshan 663000, China;3. Biological Control Institute, Chinese Academy of Agricultural Sciences, Beijing 100081, China
Abstract:Brevibacillus laterosporus YMF3.00003 strain,can effectively inhibit the mycelial growth of most phytopathogens.The highest growth inhibition rates of the liquid culture of YMF3.00003 against four tested phytopathogens,Cylindrocarpon didynum,C.destructans,Magnaporthegrisea and Rhizoctonia solani,were 81.5%,71.0%,60.7% and 60.2% respectively.In 20L biologic reaction jar,the fermentation conditions,growth curve and fungi static dynamics of the strain were determined and presented.In this jar,the highest cell number,5.1?109,was obtained after incubation of 21 hours and the culture showed the highest inhibition(90.5%) to mycelialgrowth of R.solani at 25hours after inoculation.Furthermore,sawdust was selected out of 7 tested candidates as the sorbent for formulation development and a biocontrol agent which containing about 2?1011 cells/g wasdeveloped.
Keywords:Brevibacillus laterosporus  biocontrol agent  phytopathogen  fermentation  
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