scholarly journals Chlorophyll Breakdown – How Chemistry Has Helped to Decipher a Striking Biological Enigma

Synlett ◽  
2018 ◽  
Vol 30 (03) ◽  
pp. 263-274 ◽  
Author(s):  
Bernhard Kräutler

How the fall colors arise and how chlorophyll (Chl) breakdown occurs in higher plants has remained enigmatic until three decades ago. Fundamental insights into this fascinating puzzle have been gained, meanwhile, by basic contributions from plant biology and chemistry. This short review is a personal account of key advances from synthetic, mechanistic, and structural chemistry that led to the discovery of the bilin-type Chl catabolites and helped elucidate the metabolic processes that generated them from Chl.1 Introduction2 Discovery and Structure Elucidation of a First Non-Green Chl Catabolite3 Structure Elucidation of Fleetingly Existent Blue-Fluorescent Chl Catabolites4 The Red Chl Catabolite – Key Ring-Opened Tetrapyrrole Accessed by Partial Synthesis5 Synthesis of ‘Primary’ Fluorescent Chl Catabolites by Reduction of Red Chl Catabolite6 Nonfluorescent Chl Catabolites from Isomerization of Fluorescent Chl Catabolites7 Persistent Fluorescent Chl Catabolites and Blue-Luminescent Bananas8 Discovery, Structure Elucidation, and Biological Formation of Dioxobilin-Type Chl Catabolites9 Occurrence, Partial Synthesis, and Structure of Phyllochromobilins, the Colored Bilin-Type Chl Catabolites10 Conclusion and Outlook

1982 ◽  
Vol 102 (6) ◽  
pp. 525-532 ◽  
Author(s):  
HIROMITSU TAKAYAMA ◽  
SUGIO HASEGAWA ◽  
SHINICHIRO SAKAI ◽  
JOJU HAGINIWA ◽  
TOSHIHIKO OKAMOTO

1988 ◽  
Vol 66 (10) ◽  
pp. 2103-2109 ◽  
Author(s):  
K. W. Joy

In plants, the primary input of nitrogen (obtained from the soil or from symbiotic dinitrogen fixation) occurs through the assimilation of ammonia into organic form. Synthesis of glutamine (via glutamine synthetase) is the major, and possibly exclusive, route for this process, and there is little evidence for the participation of glutamate dehydrogenase. A variety of reactions distribute glutamine nitrogen to other compounds, including transfer to amino nitrogen through glutamate synthase. In many plants asparagine is a major recipient of glutamine nitrogen and provides a mobile reservoir for transport to sites of growth; ureides perform a similar function in some legumes. Utilisation of transport forms of nitrogen, and a number of other metabolic processes, involves release of ammonia, which must be reassimilated. In illuminated leaves, there is an extensive flux of ammonia released by the photorespiratory cycle, requiring continuous efficient reassimilation. Aspects of ammonia recycling and related amide metabolism in higher plants are reviewed.


1980 ◽  
Vol 58 (20) ◽  
pp. 2121-2126 ◽  
Author(s):  
Richard J. Stonard ◽  
Raymond J. Andersen

Celenamides C (7) and D (8), two novel alkaloids closely related to peptide alkaloids found in higher plants, have been isolated as their penta (12) and nonacetyl (13) derivatives, respectively, from acetylated extracts of the sponge Clionacelata (Grant). The structure elucidation of 7 and 8 is described.


1980 ◽  
Vol 58 (23) ◽  
pp. 2592-2599 ◽  
Author(s):  
Frederick J. Brown ◽  
Ian J. Massey ◽  
Carl Djerassi

The 3α,5-cyclo-6β-methoxy (i-methyl ether) moiety is a common protective grouping in steroid partial synthesis. Therefore, the mass spectrometric behavior of 6β-hydroxy-3α,5-cyclo-5α-cholestane, the corresponding methyl, ethyl, and tert-butyl ethers, the analogous ketone, and the parent hydrocarbon has been investigated in order to determine the mechanisms of the characteristic fragmentations of these compounds. Such knowledge is essential for unequivocal structure elucidation by mass spectrometry and also bears on the current interest in the stereospecificity of electron impact induced eliminations. Deuterium labeling of carbon atoms 1,2,3,4,7,8,9, and 19 of 6β-methoxy-3α,5-cyclo-5α-cholestane established the course of methanol extrusion and the identity of the highly diagnostic A ring cleavage ion [Formula: see text] Mechanisms are proposed for these key fragmentations. The mass spectra of the methyl, ethyl, and tert-butyl ethers of cholesterol are analyzed, and the features distinguishing these compounds from the isomeric 3,5-cyclosteroids are noted.


2020 ◽  
Vol 19 (5) ◽  
pp. 668-673
Author(s):  
Steffen Jockusch ◽  
Bernhard Kräutler

Red chlorophyll catabolite, generated as an intermediate during chlorophyll breakdown in higher plants, is considered a phototoxic ‘pro-death molecule’. However, its singlet oxygen and fluorescence quantum yields are remarkably low.


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