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Studies on the unusual behaviour of bovine liver UDP-glucose dehydrogenase in assays at acid and neutral pH and on the presence of tightly bound nucleotide material in purified preparations of this enzyme.

机译:在酸性和中性pH下测定牛肝UDP-葡萄糖脱氢酶异常行为的研究,以及在该酶的纯化制剂中存在紧密结合的核苷酸物质的情况。

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摘要

Assays of UDP-glucose dehydrogenase at pH 6.0 show long (10-15 min) lag periods before the steady-state rate is established, but at pH 9.0 no lag is observed. At intermediate pH values the lag is progressively shorter as the pH becomes more alkaline. The behaviour of the enzyme in assays at neutral and acid pH depends on the pH and concentration of the enzyme used to initiate the assay. The steady-state rate at pH 6.0 is strongly concentration-dependent. It is suggested that these phenomena arise because of the slow dissociation of an inactive enzyme species to an active one. Purified preparations of the enzyme release approx. 1 mol of a UDP-sugar/mol of enzyme subunit on denaturation. The identity of the UDP-sugar is unknown.
机译:在pH值为6.0的UDP-葡萄糖脱氢酶测定显示,建立稳态速率之前有很长的滞后时间(10-15分钟),但在pH 9.0时未观察到滞后。在中等pH值下,随着pH值变得更碱性,滞后会逐渐变短。在中性和酸性pH下测定中酶的行为取决于起始测定所用的酶的pH和浓度。 pH 6.0时的稳态速率与浓度密切相关。提示这些现象是由于非活性酶物质缓慢解离为活性酶物质而产生的。纯化后的酶制剂释放约。变性时1摩尔UDP糖/摩尔的酶亚基。 UDP糖的身份未知。

著录项

  • 作者

    Dickinson, F M;

  • 作者单位
  • 年度 1988
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  • 原文格式 PDF
  • 正文语种 en
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