Green/red cyanobacteriochromes regulate complementary chromatic acclimation via a protochromic photocycle
0303 health sciences
03 medical and health sciences
Bacterial Proteins
Base Sequence
Light
Acclimatization
Molecular Sequence Data
Light-Harvesting Protein Complexes
Synechocystis
Phycobiliproteins
Phytochrome
DOI:
10.1073/pnas.1302909110
Publication Date:
2013-03-12T01:09:22Z
AUTHORS (8)
ABSTRACT
Cyanobacteriochromes (CBCRs) are cyanobacterial members of the phytochrome superfamily of photosensors. Like phytochromes, CBCRs convert between two photostates by photoisomerization of a covalently bound linear tetrapyrrole (bilin) chromophore. Although phytochromes are red/far-red sensors, CBCRs exhibit diverse photocycles spanning the visible spectrum and the near-UV (330–680 nm). Two CBCR subfamilies detect near-UV to blue light (330–450 nm) via a “two-Cys photocycle” that couples bilin
15Z/15E
photoisomerization with formation or elimination of a second bilin–cysteine adduct. On the other hand, mechanisms for tuning the absorption between the green and red regions of the spectrum have not been elucidated as of yet. CcaS and RcaE are members of a CBCR subfamily that regulates complementary chromatic acclimation, in which cyanobacteria optimize light-harvesting antennae in response to green or red ambient light. CcaS has been shown to undergo a green/red photocycle: reversible photoconversion between a green-absorbing
15Z
state (
15Z
P
g
) and a red-absorbing
15E
state (
15E
P
r
). We demonstrate that RcaE from
Fremyella diplosiphon
undergoes the same photocycle and exhibits light-regulated kinase activity. In both RcaE and CcaS, the bilin chromophore is deprotonated as
15Z
P
g
but protonated as
15E
P
r
. This change of bilin protonation state is modulated by three key residues that are conserved in green/red CBCRs. We therefore designate the photocycle of green/red CBCRs a “protochromic photocycle,” in which the dramatic change from green to red absorption is not induced by initial bilin photoisomerization but by a subsequent change in bilin protonation state.
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