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Screening and Identification of Strains Converting Trans-anethole to Anisic Acid

机译:将反式苯乙醇转化为抗溶血酸的筛选和鉴定

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[Objectives] This study was conducted to isolate and screen the bacteria that can convert trans-anethole to anisic acid from star anise and its environmental samples, and identify the bacteria. [Methods] According to the traditional microbial culture method, with trans-anethole as the sole carbon source, through enrichment culture and separation and purification, preliminary screening by thin layer chromatography and re-screening by high-performance liquid chromatography, strains that degraded trans-anethole to produce anisic acid were obtained, and 16 S rDNA sequencing and phylogenetic tree construction were performed for genetic analysis. [Results] Eleven strains that degraded trans-anethole to produce anisic acid were obtained, among which strain NT2 that produced anisic acid with a relatively high efficiency was initially identified as Pseudomonas sp. The strain’s trans-anethole degradation rate was 45.41%, and the molar production rate and cumulative concentration of anisic acid were 21.80% and 1.96 g/L, respectively. [Conclusions] Strain NT2 has a strong ability to degrade trans-anethole to produce anisic acid, and can enrich strain resources for degradation of trans-anethole to anisic acid through microbial conversion.
机译:[目标]本研究进行了分离和筛选可以将转化亚硫酸转化为来自八角茴香及其环境样品的丙酸的细菌,并鉴定细菌。 [方法]根据传统的微生物培养方法,用反式乙醇作为唯一的碳源,通过富集培养和分离和纯化,通过薄层色谱法初步筛选并通过高效液相色谱再筛选,菌株降解反式 - 获得产生丙酸的乙醇,进行16秒的RDNA测序和系统发育树结构进行遗传分析。 [结果]获得了降解反式苯乙醇产生突出酸的11株,其中菌株NT2产生具有相对高效率的突出酸,最初被鉴定为假单胞菌SP。菌株的反式苯乙醇降解率为45.41%,摩尔生产速率和抗酸的累积浓度分别为21.80%和1.96克/升。 [结论]菌株NT2具有较强的降解转甲醇以产生突出酸的能力,并且可以通过微生物转化来富集官能抗邻苯乙醇降解转甲醇的应变资源。

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