副叶氏杆菌sp C101的鉴定、培养条件及培养液的抑菌活性

Nguyen Manh Tuan, Le Quang Vien, Truong Phuc Hung, Tran Minh Quan, Do Thi Thu Hien, Do Bich Due, Duong Thi Khuyen
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摘要

近十年来,未经培养的细菌作为发现新型抗菌化合物的潜在候选者受到了特别的关注。菌株C101和C102为阴性革兰氏菌,仅在R2A/3、NB/3、LB/10和R4/10等低营养培养基上生长。在R2A/3培养基上,28℃培养6天后,分离菌菌落为圆形、凸形、柠檬黄,大小为1 ~ 1.5 mm。细胞尺寸为0.2-0.3 × 0.8-1.3µm。菌株C101和C102的生长温度为15 ~ 37℃(25 ~ 28℃),pH为5 ~ 8(6 ~ 7)。菌株C101 (MT756087)和C102 (MT756088)的16S rRNA基因序列同源性为100%。利用NCBI Blast和EzTaxon数据库对菌株C101的16S rRNA全长序列进行分析,结果显示菌株C101与未培养克隆的相似性为99.18-100%,与类群terrae SGM2-10T的相似性为97.86%。基因序列分析表明,菌株C101可能是拟生杆菌属的一个新的候选种。菌株C101在R4/10培养基中28℃振荡培养10 d后提取抑菌化合物,对2µg/L的炭素芽孢杆菌KEMB 211-146和4µg/L的金黄色葡萄球菌ATCC 6538均有抑制作用;中间抑制枯草芽孢杆菌KEMB 5201 -001浓度为8µg/L,表皮葡萄球菌ATCC 14990浓度为8µg/L,金黄色葡萄球菌CCARM 3155浓度为16µg/L;金黄色葡萄球菌CCARM 3095浓度为64µg/L,金黄色葡萄球菌CCARM 3192浓度为32µg/L,表皮葡萄球菌CCARM 3710浓度为64µg/L。
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Identification, cultivation condition of Parasevetibacter sp C101 and antimicrobial activity of the bacterial culture extract
During the recent decade, uncultured bacteria have been special interest as potential candidates for discovering novel antibacterial compounds. Two strains C101 and C102 were negative Gram bacteria, only growing on low nutrient media as R2A/3, NB/3, LB/10 and R4/10 compared to the usual. On R2A/3 medium, colonies of the isolates were round, convex, lemon yellow color with the size of 1-1.5 mm after six days of incubation at 28oC. Cells were 0.2-0.3 × 0.8-1.3 µm. The strains C101 and C102 were able to grow at temperature ranging 15-37oC (optimum at 25-28oC), pH 5-8 (optimum in pH 6-7). The sequences of 16S rRNA genes from strain C101 (MT756087) and C102 (MT756088) shared 100% identity. Analysis of full-length 16S rRNA gene sequence of strain C101 via using NCBI Blast, EzTaxon Database revealed the highest similarity of 99.18-100% to uncultured clones, and 97.86% to type species as Parasegetibacter terrae SGM2-10T. Genetic sequence analysis data showed that strain C101 should be considered a novel candidate species of the genus Parasegetibacter. Antibacterial compound was extracted from culture of strain C101 in R4/10 medium for ten days of shaking incubator at 28oC and exhibited susceptible activity to inhibit Bacillus anthracis KEMB 211-146 at a concentration of 2 µg/L and Staphylococcus aureus ATCC 6538 at 4 µg/L; intermediate inhibiting Bacillus subtilis KEMB 51201-001 at 8 µg/L, Staphylococcus epidermidis ATCC 14990 at 8 µg/L, and S. aureus CCARM 3155 at 16 µg/L; inhibition of S. aureus CCARM 3095 at 64 µg/L, S. aureus CCARM 3192 at 32 µg/L, and S. epidermidis CCARM 3710 at 64 µg/L.
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