从冷冻菌种甘油管中分离到一株生长力极强的污染细菌,该细菌能产生抑制链格孢真菌的活性物质,在研究抑菌活性物质的过程中,对这株细菌进行分类鉴定.通过传统的表型及生理生化方法,将该菌定位到芽孢杆菌属(Bacillus),与枯草芽孢杆菌(B.su...从冷冻菌种甘油管中分离到一株生长力极强的污染细菌,该细菌能产生抑制链格孢真菌的活性物质,在研究抑菌活性物质的过程中,对这株细菌进行分类鉴定.通过传统的表型及生理生化方法,将该菌定位到芽孢杆菌属(Bacillus),与枯草芽孢杆菌(B.subtilis)的相似性最大,最终确定这株菌为B.subtilis中的一个株型,即Bacillus subtilis subsp.subtilis str.168.以链格孢属真菌(包括原有的和从空气、小麦病斑分离的)为受试菌,对此株细菌产生抑菌物质的时间进行跟踪,当该菌进入稳定生长期后开始产生抑菌物质,72 h时积累达到最大值.对抑菌物质进行过滤、加热、调节pH值等多种处理,初步确定抑菌物质的特性为外泌型、脂溶性,可透过孔径0.22μm的微孔滤膜,可耐受100℃5 m in,80℃10 m in的高温,微碱性条件不影响其生物活性.展开更多
In our ongoing search for new inhibitors of 5-lipoxygenase(5-LOX) from microbial resources,Aspergillus F06Z-509 was found to produce active components.Three active compounds named F06Z-509-A,B and C were obtained an...In our ongoing search for new inhibitors of 5-lipoxygenase(5-LOX) from microbial resources,Aspergillus F06Z-509 was found to produce active components.Three active compounds named F06Z-509-A,B and C were obtained and identified as butyrolactoneⅡ,ⅠandⅢby NMR and MS data analyses.They showed inhibitory activity against 5-LOX with IC50 of 21.43, 22.51 and 11.83μg/mL,respectively.Butyrolactones are shown to be inhibitors of 5-LOX for the first time.展开更多
文摘从冷冻菌种甘油管中分离到一株生长力极强的污染细菌,该细菌能产生抑制链格孢真菌的活性物质,在研究抑菌活性物质的过程中,对这株细菌进行分类鉴定.通过传统的表型及生理生化方法,将该菌定位到芽孢杆菌属(Bacillus),与枯草芽孢杆菌(B.subtilis)的相似性最大,最终确定这株菌为B.subtilis中的一个株型,即Bacillus subtilis subsp.subtilis str.168.以链格孢属真菌(包括原有的和从空气、小麦病斑分离的)为受试菌,对此株细菌产生抑菌物质的时间进行跟踪,当该菌进入稳定生长期后开始产生抑菌物质,72 h时积累达到最大值.对抑菌物质进行过滤、加热、调节pH值等多种处理,初步确定抑菌物质的特性为外泌型、脂溶性,可透过孔径0.22μm的微孔滤膜,可耐受100℃5 m in,80℃10 m in的高温,微碱性条件不影响其生物活性.
基金National Basic Research Project of China(Grant No.2009CB526513)National New Drug Research and Development Proiect(Grant No.2008ZX09401-05)
文摘In our ongoing search for new inhibitors of 5-lipoxygenase(5-LOX) from microbial resources,Aspergillus F06Z-509 was found to produce active components.Three active compounds named F06Z-509-A,B and C were obtained and identified as butyrolactoneⅡ,ⅠandⅢby NMR and MS data analyses.They showed inhibitory activity against 5-LOX with IC50 of 21.43, 22.51 and 11.83μg/mL,respectively.Butyrolactones are shown to be inhibitors of 5-LOX for the first time.