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首页> 外文期刊>Journal of Microbiology, Biotechnology and Food Sciences >UTILIZATION OF MUSTARD OIL FOR THE PRODUCTION OF POLYHYDROXYALKANOATES BY Pseudomonas aeruginosa
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UTILIZATION OF MUSTARD OIL FOR THE PRODUCTION OF POLYHYDROXYALKANOATES BY Pseudomonas aeruginosa

机译:铜绿假单胞菌利用芥末油生产聚羟基烷酸酯

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With the unnecessary use of plastics and cumulative pressure being placed on capacities available for plastic waste disposal, the need for biodegradable plastics and biodegradation of plastic wastes has assumed increasing importance in the last few years. Bioplastic production from mustard oil was considered relatively cheap, easily available, included in vegetable oil and don’t having much volatile characteristics. Total of 67 bacterial strains were isolated and purified from different regions of the Pakistan, and were checked for Polyhydroxyalkanoates (PHA) production by Sudan black and Nile blue staining. Quantitative analysis for biodegradable plastic produced by different bacterial species was performed by Modified surfactant hypochlorite method. High PHA production was detected in 35 strains belonging to different genera including Pseudomonas, Staphylococcus, Escherichia and Enterobacter. Fermentation and PHA production was done in batch culture. The PHA production of P. aeruginosa by mustered oil cultivation was studied under six experimental conditions, such as air flow rates, pH, Temperature, optical density, substrates concentration and cell dry weight. PHA production of Pseudomonas species were subsequently authenticated at molecular level by PCR amplifications and sequence analysis. PHA polymerase 1 (PhaC1) and PHA polymerase 2 (PhaC2) from Pseudomonas aeruginosa were amplified, sequenced and submitted to gene bank.
机译:由于塑料的不必要使用以及塑料废物处理能力的累积压力,对生物可降解塑料和塑料废物进行生物降解的需求在最近几年中变得越来越重要。芥菜油的生物塑料生产被认为相对便宜,容易获得,包括在植物油中,并且挥发性不大。从巴基斯坦不同地区分离并纯化了总共67种细菌菌株,并通过苏丹黑和尼罗蓝染色检查了多羟基链烷酸酯(PHA)的产生。采用改良的表面活性剂次氯酸盐方法对不同细菌产生的可生物降解塑料进行定量分析。在包括假单胞菌,葡萄球菌,大肠埃希氏菌和肠杆菌的不同属的35个菌株中检测到高的PHA产生。发酵和PHA生产是分批培养的。在6种实验条件下研究了通过must油培养法生产的铜绿假单胞菌的PHA,这些实验条件是空气流速,pH,温度,光密度,底物浓度和细胞干重。随后通过PCR扩增和序列分析在分子水平上鉴定假单胞菌属物种的PHA产生。扩增铜绿假单胞菌的PHA聚合酶1(PhaC1)和PHA聚合酶2(PhaC2),测序并提交基因库。

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