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首页> 外文期刊>Annals of Microbiology >Screening and identification of a highly lipolytic bacterial strain from barbecue sites in Hainan and characterization of its lipase
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Screening and identification of a highly lipolytic bacterial strain from barbecue sites in Hainan and characterization of its lipase

机译:海南烧烤区高脂解细菌菌株的筛选,鉴定及其脂肪酶特性

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A cheap and rapid screening method for isolation of lipolytic bacteria was established. A total of 145 lipolytic strains were isolated from oil-contaminated soil samples at barbeque sites in Haikou, China. Highly lipolytic strains were screened based on the formation of clearance zones on turbid solid media supplemented with emulsified peanut oil. One strain, C737-11, had the highest lipolytic activity and was further analyzed. This strain had physiological and biochemical characteristics that were similar to the genus Burkholderia. Phylogenetic analysis based on the ferric uptake regulator (fur) gene sequences located the strain to the clade of Burkholderia cepacia, Genomovar I, while resolution of the phylogeny based on 16S rRNA sequences was not good enough to distinguish Burkholderia species. The fermentation conditions were optimized and the optimal medium inducing or supporting lipase production was 0.5% glucose, 2% peanut oil, 2% peptone, 0.1% (NH4)2SO4, 0.1% K2HPO4·3H2O and 0.05% MgSO4·7H2O at pH 8.0. The optimal fermentation temperature was 37°C, and the best fermentation time was 72 h. Under these optimal conditions, lipolytic activity reached 10.5 U mL−1. The lipase produced by C737-11 was thermally stable and had an optimal reaction pH of 8.0 and an optimal reaction temperature of 37°C.
机译:建立了一种廉价且快速的筛选方法来分离脂解细菌。从中国海口烧烤场的石油污染土壤样品中共分离出145种脂解菌株。基于在添加了乳化花生油的混浊固体培养基上形成的清除区,筛选了高度脂解菌株。一种菌株C737-11具有最高的脂解活性,并进行了进一步分析。该菌株具有与伯克霍尔德氏菌属相似的生理和生化特征。基于铁摄取调节剂(fur)基因序列的系统发育分析将该菌株定位到洋葱伯克霍尔德菌,Genomovar I进化枝,而基于16S rRNA序列的系统发育解析不足以区分伯克霍尔德菌种。优化了发酵条件,诱导或支持脂肪酶生产的最佳培养基为0.5%葡萄糖,2%花生油,2%蛋白ept,0.1%(NH 4 2 SO 4 ,0.1%K 2 HPO 4 ·3H 2 O和0.05%MgSO 4 ·7H 2 O。最佳发酵温度为37°C,最佳发酵时间为72 h。在这些最佳条件下,脂解活性达到10.5 U mL -1 。 C737-11产生的脂肪酶具有热稳定性,最佳反应pH为8.0,最佳反应温度为37°C。

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