Polymorphism of Fatty Acid of Ralstonia solanacearum in Fujian Province

【目的】利用气相色谱技术检测福建省的40株青枯雷尔氏菌(Ralstonia solanacearum)菌株细胞内的脂肪酸,分析其脂肪酸分布的多态性;研究青枯雷尔氏菌脂肪酸多态性与青枯雷尔氏菌现有种下分化方法之间的关系。【方法】对40株青枯雷尔氏菌脂肪酸进行气相色谱分析,比较同一寄主分离的青枯雷尔氏菌和不同寄主分离的青枯雷尔氏菌脂肪酸的分布;对40株青枯雷尔氏菌脂肪酸进行聚类分析,分析聚成的各类青枯雷尔氏菌脂肪酸的特点以及脂肪酸多态性与其生理小种、生化型和致病性之间的关系。【结果】同一寄主分离的青枯雷尔氏菌和不同寄主分离的青枯雷尔氏菌,其脂肪酸都存在着明显的多态性;对40株青枯雷尔氏菌的脂肪酸进行聚类分析,可以聚成3类,即groupⅠ、groupⅡ和groupⅢ;青枯雷尔氏菌生理小种1存在着不同的脂肪酸类群,青枯雷尔氏菌脂肪酸多态性与其生化型之间不存在相关性,但是脂肪酸和致病性之间存在一定的相关性:groupⅠ为无致病性菌株,groupⅡ为过渡性菌株,groupⅢ为强致病性菌株。【结论】福建省青枯雷尔氏菌脂肪酸分布存在着明显的多态性;青枯雷尔氏菌脂肪酸多态性与致病性之间存在一定的相关性,脂肪酸有望成为青枯雷尔氏菌小种鉴定的新指标。【Objective】The fatty acids of 40 strains of Ralstonia solanacearum isolated from different hosts in the fields in Fujian Province were detected by gas chromatography (GC). The polymorphism of R. solanacearum fatty acids relating to the pathogenicity was observed. 【Method】 The MIDI system and cluster analysis were introduced in analyzing fatty acids to display the relations among the polymorphism, race, biovartype and pathogenicity. 【Result】 The results showed that the patterns of fatty acids were significant different in R. solanacearum strains both isolated from the different hosts and the different body parts of the same hosts. According to the fatty acids the strains were clustered into three groups, e.g. group Ⅰ relating to the strains with non-pathogenicity, group Ⅱ in which the strain pathogenicity was changeable with some virulent and avirulent ones, and group Ⅲ respondent to high pathogenicity. It was proved that the model of fatty acids has no relations to races and biovartypes in R. solanacearum. 【Conclusion】It is the fist time to describe the polymorphism of fatty acids in R. solanacearum in this paper. The pathogenicity could be grouped by the models of fatty acids to distinguish the pathogenicity, which could be used in the identification of R. solanacearum under species differentiation.国家“863”项目(2002AA244031);; 福建省青年科技人才创新项目(2003.J046

Effects of Medium on Sporification of Fusarium oxysporum Schl.

选择8种培养基,采用液体培养法,研究培养基质对尖孢镰刀菌(Fusarium oxysporum Schl.)281菌株小孢子产生量的影响,结果表明,在PDA培养基上培养144h得到最大小孢子产量1.283×109cfu/ml,与其它培养基产孢量差异显著(P=0.05)。培养至192h时,ATCC培养基的小孢子数量达到1.325×109cfu/ml,与PDA培养基之间无显著差异(P=0.05),与其它6种培养基之间差异显著(P=0.05)。综合比较8种培养基,PDA培养基培养时间短,配制简单,是较为理想的产小孢子培养基。The results of eight mediums effect on sporification of Fusarium oxysporum 281 showed that the number of sporification is 1.283×109cfu/ml in PDA medium after 144h,Significant difference were observed between PDA medium and others(P=0.05).The number of sporification is 1.325×109cfu/ml in ATCC medium after 192h,there are no significant difference between ATCC and PDA medium(P=0.05).PDA medium is suitable for sporification.福建省自然科学基金“内生生防菌短芽孢杆菌GFP标记及其对黄瓜枯萎病生防机理的研究”(2006J0068);; 福建省发改委重点项目“生物农药高毒力菌株筛选利用与菌种基因资源库的建立”(闽发改投资[2006]781号

Fingerprint analysis on methyl fatty acid and its applications in microbial study

脂肪酸甲酯谱图分析方法(Fatty Acid Methyl Ester,FAME)是鉴于脂肪酸可作为生物标记物而发展起来的分析技术。本文介绍了FAME谱图分析方法及其在微生物学领域的应用,包括在微生物检测、鉴定和微生物多样性研究中的应用。Fatty acid is an important biomarker.Its application in biology research has become increasingly popular.The method of FAME fingerprint analysis is based on fatty acid's utilization as a biomarker.This paper describes the FAME fingerprint analysis and its applications for microbial studies,including identification of unknown microbes and assessment of microbial diversity.国家863计划项目(2006AA10A211);; 福建省发展和改革委员会重点项目[闽农产(2006)10号];; 福建省青年科技人才创新项目(2003.J046