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不同碳源对光暗培养下小球藻细胞中不同形式的 NADP-特异性谷氨酸脱氢酶的铵诱导的影响。

Effect of Different Carbon Sources on the Ammonium Induction of Different Forms of NADP-Specific Glutamate Dehydrogenase in Chlorella sorokiniana Cells Cultured in the Light and Dark.

机构信息

Department of Microbiology and Cell Science, University of Florida, Gainesville, Florida 32611.

出版信息

Plant Physiol. 1986 Jun;81(2):413-22. doi: 10.1104/pp.81.2.413.

Abstract

The ammonium induction of the chloroplast-localized NADP-specific glutamate dehydrogenase (NADP-GDH) was shown not to be a light-dependent process per se in Chlorella sorokiniana. In the dark without exogenous organic substrates, the cells synthesized low levels of fully active NADP-GDH, provided endogenous starch reserves had not been depleted. When cells were supplied with exogenous acetate, the rate of induction of NADP-GDH activity per milliliter of culture in the dark was equal to or slightly greater than the rate observed under photosynthetic conditions without an organic carbon source. Glucose supported only a low rate of induction of NADP-GDH activity in the dark. Both acetate and glucose inhibited induction of enzyme activity in the light. The NADP-GDH holoenzyme had at least 7 different electrophoretic forms. These forms differed in net charge and/or molecular weight. Their difference in molecular weight was due to the presence of 2 subunits with similar antigenic properties but different molecular weights (M(r) = 55,500 and 53,000; alpha-and beta-subunits, respectively). Depending upon the cultural conditions and length of the induction period, a wide variation was observed in the alpha:beta subunit ratio and in the numbers and sizes of the NADP-GDH holoenzymes.

摘要

在栅列藻中,铵盐诱导的定位于叶绿体的 NADP 特异性谷氨酸脱氢酶(NADP-GDH)本身不是一个依赖光的过程。在黑暗中没有外源有机底物的情况下,细胞合成低水平的完全活性的 NADP-GDH,只要内源性淀粉储备没有耗尽。当细胞被提供外源乙酸盐时,在黑暗中每毫升培养物中 NADP-GDH 活性的诱导速率与没有有机碳源的光合条件下观察到的诱导速率相等或略高。葡萄糖仅在黑暗中支持 NADP-GDH 活性的低诱导速率。乙酸盐和葡萄糖都抑制了酶活性在光照下的诱导。NADP-GDH 全酶至少有 7 种不同的电泳形式。这些形式在净电荷和/或分子量上有所不同。它们在分子量上的差异是由于存在 2 种具有相似抗原特性但分子量不同的亚基(Mr = 55,500 和 53,000;分别为α-和β-亚基)。根据培养条件和诱导期的长短,观察到 α:β 亚基比、NADP-GDH 全酶的数量和大小有很大的变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5426/1075350/d9f56055ffe1/plntphys00602-0096-a.jpg

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