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Comparative Analysis of Different Properties of Polyhydroxyalkanoates Isolated from Two Different Bacterial Strains: Alkaliphilus oremlandii OhILAs and Recombinant Escherichia coli XL1B

机译:从两种不同细菌菌株中分离出的多羟基链烷酸酯的不同性质的比较分析:碱性嗜碱菌Oherlandii OhILAs和重组大肠杆菌XL1B

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We synthesized poly(3-hydroxybutyrate-co-3-hydroxyvalerate) [P(3-HB-co-3-HV)] copolymer having different contents of 3-hydroxyvalerate (3-HV) units (16.04, 16.3, 24.95, 25.62, and 16.52 mol % 3-HV) with different yields of polyhydroxyalkanoates (PHAs) by feeding with different cooking oils and with Alkaliphilus oremlandii OhILAs strain. The PHA production efficiency of the Alkaiphilus strain was compared with that of the control strain, Bacillus cereus. The synthesis of each PHA biopolymer was performed with different toxic spent oils as the sole carbon source in an oil-in-water-based microemulsion medium. We observed that the productivity of the poly(3-hydroxybutyrate) [P(3-HB)] copolymer from the Alkaliphilus strain was higher than those of the PHAs isolated from B. cereus and the Escherichia coli XL1B strain. The synthesized PHA copolymers were characterized by 1H-NMR and Fourier transform infrared (FTIR) spectroscopy. In the ~1H-NMR spectra, a doublet resonance peak at 1.253 ppm of the/ methyl protons of the 3-hydroxybutyrate (3-HB) side group and one at 0.894 ppm due to the methyl protons of the 3-HV side group indicated the presence of 3-HB and 3-HV units in the copolymer. The chemical shift values at 1.25 and 2.2 ppm, due to the resonance absorption peaks of the methyl protons and methylene protons, confirmed the synthesis of the P(3-HB) homopolymer. From the FTIR spectra, a strong C@O stretching frequency in the range of 1745–1727 cm~(-1), together with strong CAO stretching bands near 1200 cm~(-1) and a strong band near 3400 cm~(-1), confirmed the synthesis of P(3-HB-co-3-HV) and P(3-HB). Thus, waste cooking oil as a substrate provided an alternate route for the formation of P(3-HB-co-3-HV) and P(3-HB) by Alkaliphilus and E. coli strains, respectively. VC 2014Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014, 131, 41080.
机译:我们合成了具有不同含量的3-羟基戊酸酯(3-HV)单元的聚(3-羟基丁酸酯-co-3-羟基戊酸酯)[P(3-HB-co-3-HV)]共聚物(16.04、16.3、24.95、25.62 ,以及通过加入不同的食用油和Alkaliphilus oremlandii OhILAs菌株饲喂而获得不同收率的多羟基链烷酸酯(PHA)的16.52 mol%3-HV)。将Alkaiphilus菌株的PHA生产效率与对照菌株蜡样芽孢杆菌(Bacillus cereus)的PHA生产效率进行了比较。在水包油基微乳液介质中,使用不同的有毒废油作为唯一碳源,进行每种PHA生物聚合物的合成。我们观察到,来自嗜碱菌菌株的聚(3-羟基丁酸酯)[P(3-HB)]共聚物的生产率高于从蜡状芽孢杆菌和大肠杆菌XL1B菌株中分离的PHA的生产率。合成的PHA共聚物通过1H-NMR和傅立叶变换红外(FTIR)光谱进行了表征。在〜1H-NMR光谱中,由于3-HV侧基的甲基质子,在3-羟基丁酸酯(3-HB)侧基的甲基质子的1.253 ppm处和在0.894 ppm处的一个质子的双峰共振峰表明。共聚物中存在3-HB和3-HV单元。由于甲基质子和亚甲基质子的共振吸收峰,在1.25和2.2 ppm处的化学位移值证实了P(3-HB)均聚物的合成。从FTIR光谱可以看出,C @ O的强拉伸频率在1745-1727 cm〜(-1)范围内,CAO的强拉伸带在1200 cm〜(-1)附近,强的C @ O拉伸带在3400 cm〜(- 1),证实了P(3-HB-co-3-HV)和P(3-HB)的合成。因此,作为基质的废食用油为分别由嗜碱菌和大肠杆菌菌株形成P(3-HB-co-3-HV)和P(3-HB)提供了另一种途径。 VC 2014,Wiley Periodicals,Inc. J. Appl。 Polym。科学2014,131,41080。

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