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Mechanism studies on the oxidation of isoeugenol by Nocardia sp. NRRL 5646.

机译:诺卡氏菌氧化异丁香酚的机理研究。 NRRL 5646。

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摘要

Essential oils contain compounds that are attractive substrates for biotransformation by microorganisms into value added flavors and fragrances. Biotransformations of aromatic aldehydes, ferulic acid, phenolic stilbenes, lignin, eugenol and isoeugenol to vanillin have been widely studied. A few reports have probed the mechanism of biotransformation of eugenol and ferulic acid to vanillin. However, there are no reports investigating the exact mechanism involved in the bioconversion of isoeugenol to vanillin or vanillic acid.; Nocardia species NRRL 5646 catalyzes the biotransformation of isoeugenol to vanillic acid and guaiacol. We proposed three reaction pathways for this biocatalytic process. One involves the oxidation of isoeugenol via coniferyl alcohol and ferulic acid; a second involves initial formation of an epoxide followed by epoxide hydrolysis, alcohol oxidation; and a third pathway is based upon initial hydration of the styrene double bond, alcohol oxidation followed by Baeyer-Villiger oxidation to vanillin.; A variety of chemical, microbial and enzymatic approaches were used to evaluate the bioconversion pathways and to detect putative intermediates. Incubations of ferulate pathway intermediates with both growing and resting Nocardia cells gave no vanillin, vanillic acid or guaiacol as products, thus ruling out this path. Incubation of the putative intermediates of the hydration pathway gave no vanillic acid, ruling out this pathway also. A racemic mixture of trans side-chain epoxides was prepared and further hydrolysis of this epoxide gave the diol. Growing cultures of Nocardia converted the epoxide to vanillic acid and the diol to vanillin suggesting that the epoxide or diol pathways were possible.; Experiments with cytochrome-P-450 inhibitors and lignostilbene-alpha,beta-dioxygenase inhibitors gave inconclusive results that would not enable the identification of these enzymes in the biotransformation process. Labeling experiments with 18O2 and H218O showed that there was incorporation of oxygen from both these sources into vanillic acid.; Experiments with cell fee preparations suggested a novel cofactorless system for this Nocardia mediated biotransformation. The enzyme involved in the conversion of isoeugenol to vanillin was partially purified. Future studies will be aimed at further purification of the oxygenase and also probing the pathway for the cofactorless bioconversion in cell-free extracts.
机译:香精油包含的化合物是有吸引力的底物,可被微生物生物转化为增值型香精和香料。芳香醛,阿魏酸,酚醛,木质素,丁子香酚和异丁香酚向香草醛的生物转化已得到广泛研究。一些报道探讨了丁香酚和阿魏酸向香草醛的生物转化机理。然而,没有报道研究异丁香酚生物转化为香草醛或香草酸的确切机理。诺卡氏菌种NRRL 5646催化异丁香酚向香草酸和愈创木酚的生物转化。我们提出了此生物催化过程的三种反应途径。一种涉及通过松柏醇和阿魏酸氧化异丁香酚。第二步是首先形成环氧化物,然后进行环氧化物水解,醇氧化。第三种途径是基于苯乙烯双键的初始水合,醇氧化,然后拜尔-维利格氧化成香兰素。各种化学,微生物和酶促方法均用于评估生物转化途径并检测假定的中间体。阿魏酸途径中间体与生长和静止的诺卡氏菌细胞一起孵育不会产生香草醛,香草酸或愈创木酚作为产物,因此排除了这种途径。水合途径的假定中间体的孵育没有产生香草酸,也排除了该途径。制备反式侧链环氧化物的外消旋混合物,并且该环氧化物的进一步水解得到二醇。不断增长的诺卡氏菌培养物将环氧化物转化为香草酸,将二醇转化为香草醛,表明环氧或二醇途径是可能的。用细胞色素-P-450抑制剂和木质素二烯-α,β-二加氧酶抑制剂进行的实验得出的结论尚不明确,无法在生物转化过程中鉴定这些酶。用18O2和H218O进行的标记实验表明,这两种来源的氧气都被掺入了香草酸中。细胞费用准备的实验表明,这种诺卡氏菌介导的生物转化是一种新型的无辅酶系统。部分纯化异丁香酚转化为香兰素的酶。未来的研究将致力于进一步纯化加氧酶,并探索无细胞提取物中无辅因子生物转化的途径。

著录项

  • 作者

    Seshadri, Ramya.;

  • 作者单位

    The University of Iowa.;

  • 授予单位 The University of Iowa.;
  • 学科 Chemistry Biochemistry.; Health Sciences Pharmacy.; Agriculture Food Science and Technology.
  • 学位 Ph.D.
  • 年度 2005
  • 页码 124 p.
  • 总页数 124
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;药剂学;农产品收获、加工及贮藏;
  • 关键词

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