Formyl groups are abundant
modifications made on the chlorophyll
(Chl) scaffold. (a) The pigments Chl b, d, and f each bear formyl groups on their macrocyclic
chlorin scaffolds at various positions. These modifications contribute
to their characteristic absorbance patterns. The modifications found
in Chl d and f are formed using
an as-yet unidentified enzyme and the photooxidoreductase Chl f synthase,1−3 respectively. Formation of the C7 formyl group in
chlorophyll(ide) b is instead proposed to be installed
via two sequential chlorophyllide a oxygenase (CAO)-catalyzed
reactions that transform the C7-methyl group of chlorophyll(ide) a into the formyl group of chlorophyll(ide) b through C7-hydroxymethyl and C7-dihydroxymethyl intermediates.10 All three chiral centers in Chl a, b, and intermediates are labeled with a red asterisk
and for the chemical structure, R = H or C20H39 for chlorophyllide and chlorophyll pigments, respectively. This
proposal for CAO is unlike that for other transformations that proceed
through more than one monooxygenation reaction and require two Rieske
oxygenases to be completed.23−25 This proposal is also unlike
that needed to convert a methyl group into a formyl group in the catabolism
of 4-toluene sulfonate, which requires both a Rieske oxygenase and
dehydrogenase.26 (b) CAO has potential
to be used as a tool for formylating the Chl scaffold to produce custom-tuned
native and non-native pigments. (c) The CAO homologues studied in
this work have different domain architectures. All homologues of CAO
are predicted to have a Rieske [2Fe-2S] cluster and a mononuclear
nonheme iron site in their catalytic domains (blue). These metallocenters
are coordinated by two His and two Cys ligands and a facial triad
of residues, respectively. The Micromonas pusilla CAO homologue is found in two polypeptide chains and the Arabidopsis thaliana and Chlamydomonas reinhardtii homologues have N-terminal regulatory domains (peach).27 As PhCAO appears to contain
the simplest architecture of all four homologues, it was the first
CAO homologue characterized in this work.