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Biosynthesis of the Modified Tetrapyrroles-the Pigments of Life

Overview
Journal J Biol Chem
Specialty Biochemistry
Date 2020 Apr 4
PMID 32241908
Citations 80
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Abstract

Modified tetrapyrroles are large macrocyclic compounds, consisting of diverse conjugation and metal chelation systems and imparting an array of colors to the biological structures that contain them. Tetrapyrroles represent some of the most complex small molecules synthesized by cells and are involved in many essential processes that are fundamental to life on Earth, including photosynthesis, respiration, and catalysis. These molecules are all derived from a common template through a series of enzyme-mediated transformations that alter the oxidation state of the macrocycle and also modify its size, its side-chain composition, and the nature of the centrally chelated metal ion. The different modified tetrapyrroles include chlorophylls, hemes, siroheme, corrins (including vitamin B), coenzyme F, heme , and bilins. After nearly a century of study, almost all of the more than 90 different enzymes that synthesize this family of compounds are now known, and expression of reconstructed operons in heterologous hosts has confirmed that most pathways are complete. Aside from the highly diverse nature of the chemical reactions catalyzed, an interesting aspect of comparative biochemistry is to see how different enzymes and even entire pathways have evolved to perform alternative chemical reactions to produce the same end products in the presence and absence of oxygen. Although there is still much to learn, our current understanding of tetrapyrrole biogenesis represents a remarkable biochemical milestone that is summarized in this review.

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References
1.
Moore S, Biedendieck R, Lawrence A, Deery E, Howard M, Rigby S . Characterization of the enzyme CbiH60 involved in anaerobic ring contraction of the cobalamin (vitamin B12) biosynthetic pathway. J Biol Chem. 2012; 288(1):297-305. PMC: 3537027. DOI: 10.1074/jbc.M112.422535. View

2.
Chen G, Canniffe D, Barnett S, Hollingshead S, Brindley A, Vasilev C . Complete enzyme set for chlorophyll biosynthesis in . Sci Adv. 2018; 4(1):eaaq1407. PMC: 5787379. DOI: 10.1126/sciadv.aaq1407. View

3.
Jost M, Simpson J, Drennan C . The Transcription Factor CarH Safeguards Use of Adenosylcobalamin as a Light Sensor by Altering the Photolysis Products. Biochemistry. 2015; 54(21):3231-4. PMC: 4455981. DOI: 10.1021/acs.biochem.5b00416. View

4.
KIKUCHI G, Kumar A, TALMAGE P, SHEMIN D . The enzymatic synthesis of delta-aminolevulinic acid. J Biol Chem. 1958; 233(5):1214-9. View

5.
Oster U, Bauer C, Rudiger W . Characterization of chlorophyll a and bacteriochlorophyll a synthases by heterologous expression in Escherichia coli. J Biol Chem. 1997; 272(15):9671-6. DOI: 10.1074/jbc.272.15.9671. View