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产氢酶介导的小球藻中亚硝酸盐还原。

Hydrogenase mediated nitrite reduction in chlorella.

机构信息

Department of Biological Sciences, Purdue University, Lafayette, Indiana.

出版信息

Plant Physiol. 1966 Feb;41(2):348-52. doi: 10.1104/pp.41.2.348.

Abstract

The assay of the hydrogenase of glucose-grown cells of Chlorella pyrenoidosa, strain 7-11-05 by means of nitrite reduction with molecular hydrogen is described. The hydrogenase of Chlorella shows maximum activity immediately after equilibration in the hydrogen atmosphere. The hydrogenase mediated reduction of nitrite to ammonia requires the presence of CO(2). However, at pH 6.4. when the reaction proceeds optimally, there is apparently sufficient retention of metabolic CO(2) to support the reaction, which goes to completion, at near maximum rates.Reduction of nitrite in the hydrogenase system when CO(2) is present results in the uptake of 3 moles of H(2) per mole of nitrite and ammonia is the product. When CO(2) is absent or limiting, ammonia is also formed from nitrite but with the uptake of less than the stoichiometric amount of H(2). It is concluded that CO(2) is essential for the uptake of H(2), and that in the absence of CO(2) internal hydrogen donors support nitrite reduction.The possibility that CO(2) exerts a catalytic effect in all reductions mediated by hydrogenase in algae is considered, and a further hypothesis, that hydrogenase arises from that portion of the photosynthetic machinery which also shows a catalytic requirement for CO(2), is proposed.

摘要

描述了用分子氢还原亚硝酸盐的方法来测定 7-11-05 藻株的葡萄糖生长细胞的氢化酶。绿球藻的氢化酶在平衡于氢气气氛中后立即显示出最大活性。氢化酶介导的亚硝酸盐还原为氨需要 CO(2)的存在。然而,在 pH 值为 6.4 时,反应最佳进行时,显然有足够的代谢 CO(2)保留来支持反应,反应以接近最大速率进行完全。当存在 CO(2)时,在氢化酶体系中亚硝酸盐的还原导致每摩尔亚硝酸盐吸收 3 摩尔 H(2),并且氨是产物。当 CO(2)不存在或有限时,也可以从亚硝酸盐形成氨,但吸收的 H(2)少于化学计量。因此,得出结论,CO(2)是吸收 H(2)所必需的,并且在没有 CO(2)的情况下,内部氢供体支持亚硝酸盐还原。考虑了 CO(2)是否在藻类中所有由氢化酶介导的还原中发挥催化作用的可能性,并提出了另一个假设,即氢化酶来自于光合作用机制的一部分,该部分也显示出对 CO(2)的催化需求。

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本文引用的文献

1
A high-temperature strain of Chlorella.一种高温型小球藻。
Science. 1953 Mar 27;117(3039):330-1. doi: 10.1126/science.117.3039.330.

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