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Identification of the diterpene cyclase and elucidation of early steps in the pseudopterosin biosynthetic pathway.

机译:二萜环化酶的鉴定和拟蝶呤生物合成途径的早期步骤的阐明。

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摘要

The pseudopterosins and seco-pseudopterosins are diterpene glycosides isolated from the marine soft coral, Pseudopterogorgia elisabethae . These compounds exhibit anti-inflammatory and analgesic activity greater than the industry standard, indomethacin. The overall goal of this research was to complete biosynthetic studies and enzymology related to the development of a biotechnological production method of the pseudopterosins and seco-pseudopterosins. We aimed to examine early steps in the biosynthetic pathway in order to gain detailed knowledge of the biosynthesis and enzymology of the system. Prior to examination of the biosynthetic pathway leading to the pseudopterosins, we developed both in vivo and in vitro systems to test putative precursors and demonstrated that pseudopterosin A is a precursor to pseudopterosins B–D.; We also identified and confirmed the intermediacy of the pseudopterosin diterpene cyclase product using a radioactivity-guided isolation. The bicyclic structure of the diterpene cyclase product suggests that the pseudopterosins and seco-pseudopterosins are derived from this common bicyclic intermediate. The isolation of the pseudopterosin diterpene cyclase product provided us with an assay for the purification of the enzyme involved in its production. We identified the diterpene cyclase in aqueous extracts of P. elisabethae and plan to utilize the amino acid sequence for identification of the gene. This represents the first isolation of a biosynthetic enzyme from a marine coral. Moreover, various characterization studies indicated that the enzyme displays certain similar characteristics to other terpenoid cyclases isolated from terrestrial sources.; In previous investigations, P. elisabethae was found only in the Bahamian and West Indian region, but we discovered P. elisabethae in the Florida Keys. Furthermore, due to the distinctive chemistry in the Florida Keys P. elisabethae, plausible early biosynthetic intermediates were isolated that are not present in the Bahamian population. We evaluated these compounds as intermediates in the biosynthesis of the pseudopterosins. The data obtained further supports the assumption of a common biosynthetic origin of the pseudopterosins and seco-pseudopterosins.
机译:拟蝶菌素和癸固-拟蝶呤是从海洋软珊瑚 Pseudopterogorgia elisabethae 中分离出的二萜糖苷。这些化合物的消炎和镇痛活性高于工业标准消炎痛。这项研究的总体目标是完成与假拟蝶菌素和粘多糖的生物技术生产方法相关的生物合成研究和酶学研究。我们旨在检查生物合成途径中的早期步骤,以获取有关系统的生物合成和酶学的详细知识。在检查导致假拟蝶菌素的生物合成途径之前,我们开发了体内体外系统以测试假定的前体,并证明了拟蝶呤A是拟蝶呤B的前体。 –D .;我们还使用放射性导向的分离方法鉴定并确认了拟蝶呤二萜环化酶产品的中间体。二萜环化酶产物的双环结构表明,假蝶呤和癸二伪蝶呤是从这种常见的双环中间体衍生而来的。拟蝶呤二萜环化酶产物的分离为我们提供了一种纯化涉及其生产的酶的方法。我们在 P的水提物中鉴定出了二萜环化酶。 Elisabethae ,并计划利用氨基酸序列来鉴定该基因。这代表了从海洋珊瑚中首次分离出生物合成酶。此外,各种表征研究表明该酶显示出与从陆地来源分离的其他萜类环化酶类似的特征。在以前的调查中, P。 elisabethae 仅在巴哈马和西印度地区发现,但我们发现了 P。佛罗里达群岛中的elisabethae 。此外,由于Florida Keys P中具有独特的化学性质。 Elisabethae ,可能的早期生物合成中间体被分离出来,这些中间体在巴哈马人中不存在。我们评估了这些化合物作为拟蝶呤生物合成的中间体。所获得的数据进一步支持了假蝶呤和山co假鳞翅目生物素的共同生物合成起源的假设。

著录项

  • 作者

    Kohl, Amber Celeste.;

  • 作者单位

    Florida Atlantic University.;

  • 授予单位 Florida Atlantic University.;
  • 学科 Chemistry Biochemistry.; Chemistry Organic.
  • 学位 Ph.D.
  • 年度 2003
  • 页码 179 p.
  • 总页数 179
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;有机化学;
  • 关键词

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