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从石油污染场地中分离和鉴定产生物表面活性剂/生物乳化剂的细菌。

Isolation and characterization of biosurfactant/bioemulsifier-producing bacteria from petroleum contaminated sites.

作者信息

Batista S B, Mounteer A H, Amorim F R, Tótola M R

机构信息

Microbiology Department, Viçosa Federal University, 36570-000 Viçosa, MG, Brazil.

出版信息

Bioresour Technol. 2006 Apr;97(6):868-75. doi: 10.1016/j.biortech.2005.04.020. Epub 2005 Jun 13.

Abstract

Biosurfactant-producing bacteria were isolated from terrestrial and marine samples collected in areas contaminated with crude oil or its byproducts. Isolates were screened for biosurfactant/bioemulsifier production in different carbon sources (glucose, fructose, sucrose and kerosene) using the qualitative drop-collapse test. Glucose produced the highest number of positive results (17 of 185 isolates). All 17 isolates produced emulsions with kerosene and 12 exhibited high emulsion-stabilizing capacity, maintaining 50% of the original emulsion volume for 48 h. Eight of the 17 isolates reduced the growth medium surface tension below 40 mN m(-1) with 5 exhibiting this capacity in cell-free filtrates. Onset of biosurfactant production differed among the isolates, with some initiating synthesis during the exponential growth phase and others after the stationary phase was reached. Increasing temperature from 25 to 35 degrees C accelerated onset of biosurfactant production in only two isolates while pH (6.5-7.6) had no effect in any isolate tested. Isolation from petroleum contaminated sites using the screening protocol presented proved to be a rapid and effective manner to identify bacterial isolates with potential industrial applications.

摘要

从受原油或其副产品污染地区采集的陆地和海洋样本中分离出了产生物表面活性剂的细菌。使用定性的液滴坍塌试验,在不同碳源(葡萄糖、果糖、蔗糖和煤油)中对分离菌株进行生物表面活性剂/生物乳化剂生产的筛选。葡萄糖产生的阳性结果数量最多(185个分离菌株中有17个)。所有17个分离菌株都能与煤油形成乳液,其中12个表现出高乳液稳定能力,能在48小时内保持原始乳液体积的50%。17个分离菌株中有8个可将生长培养基表面张力降低至40 mN m(-1)以下,其中5个在无细胞滤液中也表现出这种能力。不同分离菌株产生生物表面活性剂的起始时间不同,一些在指数生长期开始合成,另一些则在达到稳定期后开始。仅在两个分离菌株中,将温度从25℃提高到35℃会加速生物表面活性剂的产生,而pH值(6.5 - 7.6)对任何测试的分离菌株都没有影响。使用本文介绍的筛选方案从石油污染场地进行分离,被证明是一种快速有效的方法,可用于鉴定具有潜在工业应用价值的细菌分离菌株。

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