Prenylated flavin mononucleotide

Prenylated flavin mononucleotide
Names
	IUPAC name 1-Deoxy-1-(3,3,4,5-tetramethyl-9,11-dioxo-2,3,8,9,10,11-hexahydro-1H,7H-quinolino[1,8-fg]pteridin-7-yl)-D-ribitol 5-(dihydrogen phosphate)
	Systematic IUPAC name (2R,3S,4S)-2,3,4-Trihydroxy-5-(3,3,4,5-tetramethyl-9,11-dioxo-2,3,8,9,10,11-hexahydro-1H,7H-quinolino[1,8-fg]pteridin-7-yl)pentyl dihydrogen phosphate
	Other names prFMN; Prenylated FMNH2
Identifiers
3D model (JSmol)	Interactive image;
ChemSpider	61709288;
KEGG	C21215;
PubChem CID	91801161;
	InChI InChI=1S/C22H31N4O9P/c1-10-7-12-16-15(11(10)2)22(3,4)5-6-25(16)17-19(23-21(31)24-20(17)30)26(12)8-13(27)18(29)14(28)9-35-36(32,33)34/h7,13-14,18,27-29H,5-6,8-9H2,1-4H3,(H2,32,33,34)(H2,23,24,30,31)/t13-,14+,18-/m0/s1 Key: GLNFBGKHGHVPRL-IYOUNJFTSA-N;
	SMILES CC1=CC2=C3C(=C1C)C(CCN3C4=C(N2C[C@@H]([C@@H]([C@@H](COP(=O)(O)O)O)O)O)NC(=O)NC4=O)(C)C;
Properties
Chemical formula	C22H31N4O9P
Molar mass	526.483 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Prenylated flavin mononucleotide (prFMN) is a cofactor biosynthesized by the flavin prenyltransferase UbiX and used by UbiD enzymes for reversible decarboxylation reactions. Hence, prFMN is pivotal for catalysis in the ubiquitous microbial UbiD/X system.^[1]

prFMN is flavin prenylated at the N5 and C6 positions resulting in the formation of a fourth non-aromatic ring.^[2]

prFMN was discovered in 2015 at the University of Manchester by David Leys' group.^[2]^[3]

**Structure of FMN and prFMN^iminium.** The leftmost structure shows FMN (Flavin mononucleotide), the rightmost structure shows prFMN^iminium (prenylated flavin mononucleotide), Note the presence of the quaternary carbon (C3’) in prFMN^iminium indicative of cofactor prenylation.

Two studies in 2015 characterized UbiX as a flavin prenyltransferase, supplying prFMN to UbiD/Fdc1 which utilises the cofactor to catalyse a reversible decarboxylation reaction.^[2]^[3] Ferulic acid decarboxylase (Fdc1) from A. niger co-expressed in E.coli with UbiX from E.coli (AnFdc1^UbiX) once purified had clear spectral differences to singly expressed AnFdc1, and was capable of in vitro decarboxylation of a range of aromatic carboxylic acids. The atomic resolution of the crystal structure of AnFdc1^UbiX, allowed elucidation of the structure of the modified FMN cofactor classified as prFMN. The crystal structure revealed an isopentenyl-adduct to the N5-C6 of FMN, with the modifications branched nature and the position of the covalent linkages with flavin suggesting prenylation.

**prFMN^iminium in the active site of AnFDC1.** PDB file: 4ZA4.

PrFMN^Ox

UbiD activation by UbiX/prFMN was found to be dependent on oxygen suggesting that the reduced prFMN product of UbiX is oxidised to the catalytically relevant form. Several variations of the oxidised prFMN (prFMN^ox) cofactor were observed: prFMN^iminium, hydroxylated prFMN^iminium and prFMN^ketimine. Determination of the prFMN isomer that was catalytically relevant involved incubation of AnFdc1^UbiX with phenylpyruvate (of which a small proportion is α-hydroxycinnamic acid which closely resembles cinnamic acid - a model substrate). Incubation with phenylpyruvate lead to an altered UV-Vis spectrum and reversible enzyme inhibition. The crystal structure of AnFdc1^UbiX with phenylpyruvate revealed a bond between C1’ of prFMN^iminium and a phenylacetaldehyde adduct – a species that can be formed by decarboxylation of α-hydroxycinnamic acid and tautomerization of the α-hydroxystyrene prFMN^iminium adduct.

This observation confirmed that it is the prFMN^iminium that is the catalytically relevant cofactor.

References

^ Leys, David (December 2018). "Flavin metamorphosis: cofactor transformation through prenylation". Current Opinion in Chemical Biology. 47: 117–125. doi:10.1016/j.cbpa.2018.09.024. PMID 30326424.
^ ^a ^b ^c White, Mark D.; Payne, Karl A. P.; Fisher, Karl; Marshall, Stephen A.; Parker, David; Rattray, Nicholas J. W.; Trivedi, Drupad K.; Goodacre, Royston; Rigby, Stephen E. J.; Scrutton, Nigel S.; Hay, Sam; Leys, David (17 June 2015). "UbiX is a flavin prenyltransferase required for bacterial ubiquinone biosynthesis". Nature. 522 (7557): 502–506. Bibcode:2015Natur.522..502W. doi:10.1038/nature14559. PMC 4988493. PMID 26083743.
^ ^a ^b Payne, Karl A. P.; White, Mark D.; Fisher, Karl; Khara, Basile; Bailey, Samuel S.; Parker, David; Rattray, Nicholas J. W.; Trivedi, Drupad K.; Goodacre, Royston; Beveridge, Rebecca; Barran, Perdita; Rigby, Stephen E. J.; Scrutton, Nigel S.; Hay, Sam; Leys, David (17 June 2015). "New cofactor supports α,β-unsaturated acid decarboxylation via 1,3-dipolar cycloaddition". Nature. 522 (7557): 497–501. Bibcode:2015Natur.522..497P. doi:10.1038/nature14560. PMC 4988494. PMID 26083754.

[1] Leys, David (December 2018). "Flavin metamorphosis: cofactor transformation through prenylation". Current Opinion in Chemical Biology. 47: 117–125. doi:10.1016/j.cbpa.2018.09.024. PMID 30326424.

[Payne_2015-2] White, Mark D.; Payne, Karl A. P.; Fisher, Karl; Marshall, Stephen A.; Parker, David; Rattray, Nicholas J. W.; Trivedi, Drupad K.; Goodacre, Royston; Rigby, Stephen E. J.; Scrutton, Nigel S.; Hay, Sam; Leys, David (17 June 2015). "UbiX is a flavin prenyltransferase required for bacterial ubiquinone biosynthesis". Nature. 522 (7557): 502–506. Bibcode:2015Natur.522..502W. doi:10.1038/nature14559. PMC 4988493. PMID 26083743.

[White_2015-3] Payne, Karl A. P.; White, Mark D.; Fisher, Karl; Khara, Basile; Bailey, Samuel S.; Parker, David; Rattray, Nicholas J. W.; Trivedi, Drupad K.; Goodacre, Royston; Beveridge, Rebecca; Barran, Perdita; Rigby, Stephen E. J.; Scrutton, Nigel S.; Hay, Sam; Leys, David (17 June 2015). "New cofactor supports α,β-unsaturated acid decarboxylation via 1,3-dipolar cycloaddition". Nature. 522 (7557): 497–501. Bibcode:2015Natur.522..497P. doi:10.1038/nature14560. PMC 4988494. PMID 26083754.

[1]

[2]

[3]

PrFMNOx

References

PrFMN^Ox