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海洋细菌生产多不饱和脂肪酸。

Polyunsaturated fatty acid production by marine bacteria.

机构信息

School of Chemical Engineering and Advanced Materials, Newcastle University, Newcastle Upon Tyne, UK,

出版信息

Bioprocess Biosyst Eng. 2013 Nov;36(11):1641-52. doi: 10.1007/s00449-013-0936-0. Epub 2013 Mar 23.

Abstract

Polyunsaturated fatty acids are important in maintaining human health. Limitations associated with current sources of ω-3 fatty acids and ω-6 fatty acids, from animal and plant sources, have led to increased interest in microbial production. Marine bacteria may provide a suitable alternative, although the isolation of production strains and the identification of operating conditions must be addressed before manufacturing processes become economically viable. Marine isolate 560 was identified as an eicosapentaenoic acid (EPA) producer via GC/MS. The isolate was initially identified as Vibrio cyclitrophicus by 16S rRNA sequencing. Statistically based experimental designs were applied to the optimisation of medium components and environmental factors for the production of EPA. A Plackett-Burman design was used to screen for the effect of temperature, pH, and media components. Subsequently, the concentrations of NaCl, yeast extract, and peptone, identified as significant factors, were optimised using a central composite design. The predicted optimal combination of media components for maximum EPA production (4.8 mg/g dry weight) was determined as 7.9 g/l peptone, 16.2 g/l NaCl, and 6.2 g/l yeast extract. On transfer of this process to bioreactor cultivation, where a range of pH and DO values were tested, the maximum amount of EPA produced increased to 7.5 mg/g dry weight and 10 % of the total fatty acid.

摘要

多不饱和脂肪酸对维持人体健康很重要。目前从动植物来源获得的 ω-3 脂肪酸和 ω-6 脂肪酸存在一些局限性,这促使人们对微生物生产产生了浓厚的兴趣。海洋细菌可能是一种合适的替代品,不过,在制造工艺具有经济可行性之前,必须分离生产菌株并确定操作条件。通过 GC/MS 分析,鉴定海洋分离株 560 为二十碳五烯酸 (EPA) 产生菌。该分离株最初通过 16S rRNA 测序鉴定为弧菌属(Vibrio cyclitrophicus)。采用基于统计学的实验设计优化 EPA 生产的培养基成分和环境因素。采用 Plackett-Burman 设计筛选温度、pH 和培养基成分的影响。随后,采用中心组合设计优化被鉴定为显著因素的 NaCl、酵母提取物和蛋白胨的浓度。确定最大 EPA 产量(4.8 mg/g 干重)的最佳培养基成分组合为:7.9 g/L 蛋白胨、16.2 g/L NaCl 和 6.2 g/L 酵母提取物。将此过程转移到生物反应器培养中,测试了一系列 pH 和 DO 值,最大 EPA 产量增加到 7.5 mg/g 干重和 10%的总脂肪酸。

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