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叶绿体生物发生:高等植物中通过酸性和完全酯化的生物合成分支合成原叶绿素(酸)。

Chloroplast biogenesis: biosynthesis of protochlorophyll(ide) via acidic and fully esterified biosynthetic branches in higher plants.

作者信息

McCarthy S A, Mattheis J R, Rebeiz C A

出版信息

Biochemistry. 1982 Jan 19;21(2):242-7. doi: 10.1021/bi00531a007.

DOI:10.1021/bi00531a007
PMID:7074012
Abstract

The operation of two parallel biosynthetic pathways during the biosynthesis of the protochlorophyll(ide) pool of cucumber cotyledons was probed with the use of several [14C]tetrapyrroles in vitro. A comparison of the ratio (R) of delta-amino[14C]levulinic acid incorporation into protochlorophyllide/14C incorporation into protochlorophyllide ester with other incorporation ratios, RX, where X represents any of several [14C]tetrapyrrole substrates, allowed us to determine which exogenous 14C-labeled substrate was common precursor of protochlorophyllide and protochlorophyllide ester and which one was not. From such comparisons, a biosynthetic pathway of protochlorophyll(ide) biosynthesis is inferred. According to this pathway, protochlorophyllide is formed via an acidic (mono/dicarboxylic) biosynthetic branch, while protochlorophyllide ester is formed via a fully esterified (neutral) biosynthetic branch. The two biosynthetic branches are linked together by porphyrin ester synthetases at the level of protochlorophyllides and possibly at the level of the photoporphyrin IX and the magnesium protoporphyrin monoester pools.

摘要

利用几种[14C]四吡咯在体外探究了黄瓜子叶原叶绿素(酸)池生物合成过程中两条平行生物合成途径的运作情况。通过比较δ-氨基[14C]乙酰丙酸掺入原叶绿素酸的比例(R)与[14C]掺入原叶绿素酸酯的比例,以及其他掺入比例RX(其中X代表几种[14C]四吡咯底物中的任何一种),我们得以确定哪种外源14C标记底物是原叶绿素酸和原叶绿素酸酯的共同前体,哪种不是。通过此类比较,推断出了原叶绿素(酸)生物合成的一条生物合成途径。根据该途径,原叶绿素酸是通过酸性(单/二羧酸)生物合成分支形成的,而原叶绿素酸酯是通过完全酯化(中性)生物合成分支形成的。这两条生物合成分支在原叶绿素酸水平上,可能还在光卟啉IX和镁原卟啉单酯池水平上,由卟啉酯合成酶连接在一起。

相似文献

1
Chloroplast biogenesis: biosynthesis of protochlorophyll(ide) via acidic and fully esterified biosynthetic branches in higher plants.叶绿体生物发生:高等植物中通过酸性和完全酯化的生物合成分支合成原叶绿素(酸)。
Biochemistry. 1982 Jan 19;21(2):242-7. doi: 10.1021/bi00531a007.
2
Chloroplast biogenesis. Detection of monovinyl protochlorophyll(ide) b in plants.叶绿体生物发生。植物中单乙烯基原叶绿素(酯)b的检测。
J Biol Chem. 1991 Sep 15;266(26):17151-7.
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Chloroplast biogenesis. Demonstration of the monovinyl and divinyl monocarboxylic routes of chlorophyll biosynthesis in higher plants.叶绿体生物发生。高等植物中叶绿素生物合成的单乙烯基和二乙烯基单羧酸途径的证明。
J Biol Chem. 1986 Oct 15;261(29):13556-64.
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Chloroplast biogenesis. Net synthesis of protochlorophyllide from magnesium-protoporphyrin monoester by developing chloroplasts.叶绿体生物发生。发育中的叶绿体从单酯镁原卟啉净合成原叶绿素酸酯。
J Biol Chem. 1977 Jun 25;252(12):4022-4.
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Chloroplast biogenesis. Net synthesis of protochlorophyllide from protoporphyrin IX by developing chloroplasts.叶绿体生物发生。发育中的叶绿体由原卟啉IX净合成原叶绿素酸酯。
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Chloroplast Biogenesis 31: DETECTION OF AN INHIBITOR OF PROTOCHLOROPHYLL BIOSYNTHESIS IN CUCUMBER COTYLEDONS.叶绿体生物发生 31:在黄瓜子叶中检测到原叶绿素生物合成的抑制剂。
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Chloroplast biogenesis: quantitative determination of monovinyl and divinyl Mg-protoporphyrins and protochlorophyll(ides) by spectrofluorometry.叶绿体生物合成:通过荧光光谱法对单乙烯基和二乙烯基镁原卟啉及原叶绿素(酯)进行定量测定。
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Chloroplast culture: the chlorophyll repair potential of mature chloroplasts incubated in a simple medium.叶绿体培养:在简单培养基中培养的成熟叶绿体的叶绿素修复潜力。
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Protochlorophyll biosynthesis in a cell-free system from higher plants.高等植物无细胞系统中的原叶绿素生物合成。
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Chloroplast biogenesis: detection of a magnesium protoporphyrin diester pool in plants.叶绿体生物发生:植物中镁原卟啉二酯池的检测
Biochemistry. 1981 Aug 18;20(17):5080-7. doi: 10.1021/bi00520a039.

引用本文的文献

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Accumulation of photodynamic tetrapyrroles induced by acifluorfen-methyl.乙羧氟草醚甲酯诱导的光动力四吡咯的积累
Plant Physiol. 1988 Jul;87(3):632-7. doi: 10.1104/pp.87.3.632.
2
Chloroplast Biogenesis 60 : Conversion of Divinyl Protochlorophyllide to Monovinyl Protochlorophyllide in Green(ing) Barley, a Dark Monovinyl/Light Divinyl Plant Species.叶绿体生物发生 60 期:绿(化)大麦中二乙烯基原叶绿素ide 向单乙烯基原叶绿素ide 的转化,一种暗单乙烯基/光二乙烯基植物物种。
Plant Physiol. 1988 May;87(1):89-94. doi: 10.1104/pp.87.1.89.
3
Chlorophyll a biosynthetic routes and chlorophyll a chemical heterogeneity in plants.
植物中叶绿素a的生物合成途径及叶绿素a的化学异质性
Mol Cell Biochem. 1983;57(2):97-125. doi: 10.1007/BF00849189.