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纤细裸藻中由谷氨酸合成δ-氨基乙酰丙酸:无叶绿素突变体中酶水平的光控

delta-Aminolevulinic Acid Biosynthesis from Glutamatein Euglena gracilis: Photocontrol of Enzyme Levels in a Chlorophyll-Free Mutant.

作者信息

Mayer S M, Beale S I

机构信息

Division of Biology and Medicine, Brown University, Providence, Rhode Island 02912.

出版信息

Plant Physiol. 1991 Nov;97(3):1094-102. doi: 10.1104/pp.97.3.1094.

Abstract

Wild-type Euglena gracillis cells synthesize the key chlorophyll precursor, delta-aminolevulinic acid (ALA), from glutamate in their plastids. The synthesis requires transfer RNA(Glu) (tRNA(Glu)) and the three enzymes, glutamyl-tRNA synthetase, glutamyl-tRNA reductase, and glutamate-1-semialdehyde aminotransferase. Non-greening mutant Euglena strain W(14)ZNaIL does not synthesize ALA from glutamate and is devoid of the required tRNA(Glu). Other cellular tRNA(Glu)s present in the mutant cells were capable of being charged with glutamate, but the resulting glutamyl-tRNAs did not support ALA synthesis. Surprisingly, the mutant cells contain all three of the enzymes, and their cell extracts can convert glutamate to ALA when supplemented with tRNA(Glu) obtained from wild-type cells. Activity levels of the three enzymes were measured in extracts of cells grown under a number of light conditions. All three activities were diminished in extracts of cells grown in complete darkness, and full induction of activity required 72 hours of growth in the light. A light intensity of 4 microeinsteins per square meter per second was sufficient for full induction. Blue light was as effective as white light, but red light was ineffective, in inducing extractable enzyme activity above that of cells grown in complete darkness, indicating that the light control operates via the nonchloroplast blue light receptor in the mutant cells. Of the three enzyme activities, the one that is most acutely affected by light is glutamate-1-semialdehyde aminotransferase, as has been previously shown for wild-type Euglena cells. These results indicate that the enzymes required for ALA synthesis from glutamate are present in an active form in the nongreening mutant cells, even though they cannot participate in ALA formation in these cells because of the absence of the required tRNA(Glu), and that the activity of all three enzymes is regulated by light. Because the absence of plastid tRNA(Glu) precludes the synthesis of proteins within the plastids, the three enzymes must be synthesized in the cytoplasm and their genes encoded in the nucleus in Euglena.

摘要

野生型纤细裸藻细胞在其质体中由谷氨酸合成关键的叶绿素前体δ-氨基乙酰丙酸(ALA)。该合成过程需要转运RNA(Glu)(tRNA(Glu))以及三种酶,即谷氨酰-tRNA合成酶、谷氨酰-tRNA还原酶和谷氨酸-1-半醛转氨酶。非绿化突变型裸藻菌株W(14)ZNaIL不能由谷氨酸合成ALA,并且缺乏所需的tRNA(Glu)。突变细胞中存在的其他细胞tRNA(Glu)能够被谷氨酸氨酰化,但生成的谷氨酰-tRNA不支持ALA合成。令人惊讶的是,突变细胞含有所有三种酶,并且当补充从野生型细胞获得的tRNA(Glu)时,其细胞提取物可以将谷氨酸转化为ALA。在多种光照条件下生长的细胞提取物中测定了这三种酶的活性水平。在完全黑暗中生长的细胞提取物中,所有三种活性均降低,并且活性的完全诱导需要在光照下生长72小时。每秒每平方米4微爱因斯坦的光强度足以实现完全诱导。蓝光诱导可提取酶活性的效果与白光一样有效,但红光无效,这表明光控制是通过突变细胞中的非叶绿体蓝光受体起作用的。在这三种酶活性中,如先前在野生型裸藻细胞中所显示的那样,受光影响最严重的是谷氨酸-1-半醛转氨酶。这些结果表明,从谷氨酸合成ALA所需的酶以活性形式存在于非绿化突变细胞中,尽管由于缺乏所需的tRNA(Glu),它们不能参与这些细胞中的ALA形成,并且所有三种酶的活性都受光调节。由于质体tRNA(Glu)的缺失排除了质体内蛋白质的合成,因此这三种酶必须在细胞质中合成,并且它们的基因在裸藻中编码于细胞核中。

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