Literature DB >> 7793979

Phycobilin biosynthesis: reductant requirements and product identification for heme oxygenase from Cyanidium caldarium.

G Rhie1, S I Beale.   

Abstract

Algal heme oxygenase is a soluble enzyme from Cyanidium caldarium that catalyzes the first committed step of phycobilin biosynthesis by converting protoheme to biliverdin IX alpha. Although the physiological substrate (protoheme) of algal heme oxygenase is identical to that of microsomal heme oxygenase, which catalyzes heme catabolism in animals, the two enzyme systems differ in several respects including the nature of the required reductants and solubility of the enzymes. Addition of the strong Fe3+ ion chelators, desferrioxamine and Tiron (4,5-dihydroxy-1,3-benzenedisulfonic acid), greatly increased the yield of solvent-extracted bilin product. The effect of the Fe3+ chelators was approximately equal whether they were added during or after the enzyme incubation. Postincubation treatment of the enzyme reaction mixture with strong acid also greatly increased the product yield. Addition of desferrioxamine to the reaction mixture after the incubation was terminated caused the appearance of an absorption spectrum, indicating an increase in the concentration of free bilin product. Acid and Fe3+ chelators are known to cause dissociation of Fe(III)-bilin complexes. These results indicate that the in vitro enzymic reaction product of algal heme oxygenase is a nonenzyme-bound Fe(III)-biliverdin IX alpha complex that is poorly extracted and/or quantitated unless it is first dissociated. Algal heme oxygenase required the simultaneous presence of both reduced ferredoxin and a second reductant such as ascorbate for activity. The requirement for L-ascorbate could be substituted by Trolox (6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid) or D-ascorbate, but not by dehydroascorbate or dithiothreitol. Heme oxygenase was purified over 200-fold from C. caldarium by differential (NH4)2SO4 precipitation and serial column chromatography over reactive blue 2-Sepharose, DEAE-cellulose, Sephadex G-75, and ferredoxin-Sepharose.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7793979     DOI: 10.1006/abbi.1995.1358

Source DB:  PubMed          Journal:  Arch Biochem Biophys        ISSN: 0003-9861            Impact factor:   4.013


  7 in total

1.  Expression and biochemical properties of a ferredoxin-dependent heme oxygenase required for phytochrome chromophore synthesis.

Authors:  Takuya Muramoto; Noriyuki Tsurui; Matthew J Terry; Akiho Yokota; Takayuki Kohchi
Journal:  Plant Physiol       Date:  2002-12       Impact factor: 8.340

Review 2.  Thiol/Disulfide redox switches in the regulation of heme binding to proteins.

Authors:  Stephen W Ragsdale; Li Yi
Journal:  Antioxid Redox Signal       Date:  2010-12-27       Impact factor: 8.401

3.  Purification and biochemical properties of phytochromobilin synthase from etiolated oat seedlings.

Authors:  M T McDowell; J C Lagarias
Journal:  Plant Physiol       Date:  2001-08       Impact factor: 8.340

4.  The Arabidopsis photomorphogenic mutant hy1 is deficient in phytochrome chromophore biosynthesis as a result of a mutation in a plastid heme oxygenase.

Authors:  T Muramoto; T Kohchi; A Yokota; I Hwang; H M Goodman
Journal:  Plant Cell       Date:  1999-03       Impact factor: 11.277

5.  Structural and biochemical characterization of the bilin lyase CpcS from Thermosynechococcus elongatus.

Authors:  Christina M Kronfel; Alexandre P Kuzin; Farhad Forouhar; Avijit Biswas; Min Su; Scott Lew; Jayaraman Seetharaman; Rong Xiao; John K Everett; Li-Chung Ma; Thomas B Acton; Gaetano T Montelione; John F Hunt; Corry E C Paul; Tierna M Dragomani; M Nazim Boutaghou; Richard B Cole; Christian Riml; Richard M Alvey; Donald A Bryant; Wendy M Schluchter
Journal:  Biochemistry       Date:  2013-11-19       Impact factor: 3.162

6.  Partial Purification and Characterization of Red Chlorophyll Catabolite Reductase, a Stroma Protein Involved in Chlorophyll Breakdown.

Authors:  S. Rodoni; F. Vicentini; M. Schellenberg; P. Matile; S. Hortensteiner
Journal:  Plant Physiol       Date:  1997-10       Impact factor: 8.340

7.  Scalable production of biliverdin IXα by Escherichia coli.

Authors:  Dong Chen; Jason D Brown; Yukie Kawasaki; Jerry Bommer; Jon Y Takemoto
Journal:  BMC Biotechnol       Date:  2012-11-23       Impact factor: 2.563

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.