首页|油茶炭疽病拮抗细菌Y13主要抑菌物质分离纯化及作用方式

油茶炭疽病拮抗细菌Y13主要抑菌物质分离纯化及作用方式

扫码查看
油茶内生拮抗细菌Y13是一株对油茶炭疽病菌有较强抑制作用的枯草芽胞杆菌.为了确定其抑菌物质的成分组成及其对油荼炭疽病菌的作用方式,本文通过乙醇沉淀、固相萃取、反相高效液相色谱法及LC-MS对抑菌物质进行分离鉴定.一共分离纯化出16个活性组分,保留时间在10.5~26.0 min的8个组分对于油茶炭疽病菌产生明显的抑菌圈,其中保留时间为11.0 min处的色谱峰抑菌效果最强,经质谱初步鉴定确定该化合物的分子量为1 042.56 u;保留时间在27.5~39.5 min的8个组分导致油茶炭疽病病原菌菌丝颜色加深,其中以保留时间37.5 min处的色谱峰效果最为明显,质谱鉴定该化合物的分子量为1 480.85 u.显微观察发现它们通过导致菌丝断裂、畸形、原生质凝集的方式抑制菌丝生长;通过使孢子畸形、膨大、消融而抑制孢子萌发.
Isolation and purification of antimicrobial substance produced by endophytic bacteria Y13 in the Camellia and its inhibitory effect on Camellia anthracnose
Bacillus subtilis strain Y13 isolated from Camellia has strong inhibitory activity against Colletotrichum gloeosporioides.In order to identify the antimicrobial compounds and the inhibition mechanism against C.gloeosporioides,the antimicrobial substances were isolated and purified by ethanol precipitation,solid phase extraction and reversed phase high performance liquid chromatography.Antifungal activity assay indicated that 16 main peak fractions had inhibition activity.The 16 main peak fractions can be divided in two groups.One group at retention time from 10.5 min to 26.0 min showed inhibition activity.The peak fraction at retention time 11.0 min showed the strongest activity and the molecular weight was 1 042.56 u identified by LC-MS.The other group at retention time from 27.5 min to 39.5 min dark the mycelia of C.gloeosporioides.The compound at retention time 37.5 min showed the strongest activity and the molecular weight was 1 480.85 u.Microscope observation revealed that the 2 compounds could break up and enlarge the mycelia,deform and swell the spores,and inhibit the spore germination.

Camellia anthracnoseantagonistic bacteriaantimicrobial substanceisolation and purificationinhibition mechanism

孟庆敏、周国英、刘君昂、左杰、董文统、王瑞芹

展开 >

中南林业科技大学经济林培育与保护教育部重点实验室,长沙410004

油茶炭疽病 拮抗细菌 抑菌物质 分离纯化 作用方式

国家自然科学基金湖南省研究生科研创新项目中南林业科技大学研究生科技创新资助项目

31170598CX2013B356CX2013B25

2014

植物保护
中国植物保护学会 中国农业科学院植物保护研究所

植物保护

CSTPCDCSCD北大核心
影响因子:1.004
ISSN:0529-1542
年,卷(期):2014.40(2)
  • 7
  • 11