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Isolation and characterization of a novel gossypol-degrading bacteria Bacillus subtilis strain Rumen Bacillus Subtilis

机译:新型棉酚降解细菌枯草芽孢杆菌菌株瘤胃芽孢杆菌的分离与表征

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摘要

Objective The aim of the study was to isolate gossypol-degrading bacteria and to assess its potential for gossypol degradation. Methods Rumen liquid was collected from fistulated cows grazing the experimental pasture. Approximately 1 mL of the rumen liquid was spread onto basal medium plates containing 2 g/L gossypol as the only source of carbon and was then cultured at 39°C to isolate gossypol-degrading bacteria. The isolated colonies were cultured for 6 h and then their size and shape observed by microscope and scanning electron microscope. The 16S rRNA gene of isolated colonies was sequenced and aligned using National Center for Biotechnology Information-Basic Local Alignment Search Tool. The various fermentation conditions, initial pH, incubation temperature, inoculum level and fermentationperiod were analyzed in cottonseed meal (CSM). The crude protein (CP), total gossypol (TG), and free gossypol (FG) were determined in CSM after fermentation with isolated strain at 39°C for 72 h. Results Screening results showed that a single bacterial isolate, named Rumen Bacillus Subtilis (RBS), could use gossypol as a carbon source. The bacterium was identified by 16S rDNA sequencing as being 98% homologous to the sequence of Bacillus subtilis strain GH38. The optimum fermentation conditions were found to be 72 h, 39°C, pH 6.5, moisture 50%, inoculum level 107 cell/g. In the optimum fermentation conditions, the FG and TG content in fermented CSM decreased 78.86% and 49% relative to the control. The content of CP and the essential amino acids of the fermented CSM increased respectively, compared with the control. Conclusion The isolation of a gossypol-degrading bacterium from the cow rumen is of great importance for gossypol biodegradation and may be a valuable potential source for gossypol-degradation of CSM.
机译:目的本研究的目的是分离棉酚降解菌,并评估其对棉酚降解潜力。方法瘤胃液体从瘘管奶牛放牧实验牧场收集。约1mL瘤胃液体的涂布在含有2g / L棉酚作为碳的唯一来源基础培养基平板上,然后在39℃下培养以分离棉酚降解细菌。的分离的菌落6小时进行培养,然后它们的大小和形状通过显微镜和扫描电子显微镜观察。分离的菌落的16S rRNA基因测序,并用国家生物技术信息中心,基本局部比对搜索工具对齐。各种发酵条件,初始pH值,培养温度,接种水平和fermentationperiod在棉籽粕(CSM)进行了分析。粗蛋白(CP),总棉酚(TG),和游离棉酚(FG)在CSM在39被确定与分离的菌株发酵后℃下72小时。结果筛选结果表明,单一的细菌分离物,命名为瘤胃枯草芽孢杆菌(RBS),可以使用棉酚作为碳源。该细菌被鉴定的16S rDNA序列为98%的同源性的枯草芽孢杆菌菌株GH38序列。发现的最佳发酵条件为72小时,39℃,pH为6.5,水分50%,接种水平107细胞/克。在最佳的发酵条件,发酵CSM的FG和TG含量降低78.86%,并且相对于对照的49%。 CP和发酵CSM的必需氨基酸的含量分别增加,与对照组相比。结论从奶牛瘤胃中棉酚降解菌的分离是对棉酚的生物降解非常重要,可能是CSM棉酚降解了宝贵的潜在来源。

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