| Literature DB >> 33975960 |
Weiqing Zhang1,2, Robert D Willows2, Rui Deng1, Zheng Li1, Mengqi Li1, Yan Wang1, Yunling Guo1, Weida Shi1, Qiuling Fan3, Shelley S Martin4, Nathan C Rockwell4, J Clark Lagarias5, Deqiang Duanmu6.
Abstract
Biosyntheses of chlorophyll and heme in oxygenic phototrophs share a common trunk pathway that diverges with insertion of magnesium or iron into the last common intermediate, protoporphyrin IX. Since both tetrapyrroles are pro-oxidants, it is essential that their metabolism is tightly regulated. Here, we establish that heme-derived linear tetrapyrroles (bilins) function to stimulate the enzymatic activity of magnesium chelatase (MgCh) via their interaction with GENOMES UNCOUPLED 4 (GUN4) in the model green alga Chlamydomonas reinhardtii A key tetrapyrrole-binding component of MgCh found in all oxygenic photosynthetic species, CrGUN4, also stabilizes the bilin-dependent accumulation of protoporphyrin IX-binding CrCHLH1 subunit of MgCh in light-grown C. reinhardtii cells by preventing its photooxidative inactivation. Exogenous application of biliverdin IXα reverses the loss of CrCHLH1 in the bilin-deficient heme oxygenase (hmox1) mutant, but not in the gun4 mutant. We propose that these dual regulatory roles of GUN4:bilin complexes are responsible for the retention of bilin biosynthesis in all photosynthetic eukaryotes, which sustains chlorophyll biosynthesis in an illuminated oxic environment.Entities:
Keywords: bilin reductase; heme oxygenase; photosynthesis; phycocyanobilin; reactive oxygen species
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Year: 2021 PMID: 33975960 PMCID: PMC8158021 DOI: 10.1073/pnas.2104443118
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205