Squalene/phytoene synthase family
| SQS_PSY | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Identifiers | |||||||||
| Symbol | SQS_PSY | ||||||||
| Pfam | PF00494 | ||||||||
| InterPro | IPR002060 | ||||||||
| PROSITE | PDOC00802 | ||||||||
| SCOP2 | 1ezf / SCOPe / SUPFAM | ||||||||
| OPM superfamily | 297 | ||||||||
| OPM protein | 3v66 | ||||||||
| Membranome | 635 | ||||||||
| |||||||||
The squalene/phytoene synthase family represents proteins that catalyze the head-to-head condensation of C15 and C20 prenyl units (i.e. farnesyl diphosphate and genranylgeranyl diphosphate). This enzymatic step constitutes part of steroid and carotenoid biosynthesis pathway. Squalene synthase EC (SQS) and Phytoene synthase EC (PSY) are two well-known examples of this protein family and share a number of functional similarities. These similarities are also reflected in their primary structure.[1][2][3] In particular three well conserved regions are shared by SQS and PSY; they could be involved in substrate binding and/or the catalytic mechanism. SQS catalyzes the conversion of two molecules of farnesyl diphosphate (FPP) into squalene. It is the first committed step in the cholesterol biosynthetic pathway. The reaction carried out by SQS is catalyzed in two separate steps: the first is a head-to-head condensation of the two molecules of FPP to form presqualene diphosphate; this intermediate is then rearranged in a NADP-dependent reduction, to form squalene:
2 FPP -> presqualene diphosphate + NADP -> squalene
SQS is found in all three domains of life; eukaryotes, archaea (haloarchaea) and bacteria. A recent phylogenetic analysis suggests a bacterial origin of SQS[4] and a later horizontal transfer of the SQS gene to a common ancestor of eukaryotes. Some bacteria are known to alternatively possess a set of three genes to biosynthesize squalene (HpnCDE).[5] HpnC and HpnD are homologous to each other and seem to have co-evolved in HpnCDE-containing species, together with HpnE. HpnCD are further homologous to SQS and PSY and thus are members of the squalene/phytoene synthase family. HpnCD and SQS are inferred to have evolved independently from a PSY homolog.[4]
In yeast, SQS is encoded by the ERG9 gene, in mammals by the FDFT1 gene. SQS is membrane-bound.
PSY catalyzes the conversion of two molecules of geranylgeranyl diphosphate (GGPP) into phytoene. It is the second step in the biosynthesis of carotenoids from isopentenyl diphosphate. The reaction carried out by PSY is catalyzed in two separate steps: the first is a head-to-head condensation of the two molecules of GGPP to form prephytoene diphosphate; this intermediate is then rearranged to form phytoene.
2 GGPP -> prephytoene diphosphate -> phytoene
PSY is found in all organisms that synthesize carotenoids: plants and photosynthetic bacteria as well as some non-photosynthetic bacteria and fungi. In bacteria PSY is encoded by the gene crtB. In plants PSY is localized in the chloroplast. While PSY/CrtB catalyzes the head-to-head condensation for the C20 prenyl unit (GGPP), a group of homologous proteins labelled as CrtM catalyze the same enzymatic reaction for the C15 unit (FPP).[6] The product of two FPP condensation is dehydrosqualene (diapophytoene). CrtB and CrtM share a common ancestry, but it is not known which evolved first.
While the substrates FPP and GGPP are amphipathic, the products squalene, dehydrosqualene and phytoene are all hydrophobic. Thus, the subsequent enzymatic steps in the steroid and carotenoid biosynthesis take place in the cellular membranes of host organisms.
References
[edit]- ^ Summers C, Karst F, Charles AD (December 1993). "Cloning, expression and characterisation of the cDNA encoding human hepatic squalene synthase, and its relationship to phytoene synthase". Gene. 136 (1–2Che): 185–92. doi:10.1016/0378-1119(93)90462-c. PMID 8294001.
- ^ Robinson GW, Tsay YH, Kienzle BK, Smith-Monroy CA, Bishop RW (May 1993). "Conservation between human and fungal squalene synthetases: similarities in structure, function, and regulation". Mol. Cell. Biol. 13 (5): 2706–17. doi:10.1128/mcb.13.5.2706. PMC 359645. PMID 8474436.
- ^ Ramer S, Hugueney P, Bouvier F, Camara B, Kuntz M (November 1993). "Expression of the genes encoding the early carotenoid biosynthetic enzymes in Capsicum annuum". Biochem. Biophys. Res. Commun. 196 (3): 1414–21. doi:10.1006/bbrc.1993.2410. PMID 8250898.
- ^ a b Santana-Molina, Carlos; Rivas-Marin, Elena; Rojas, Ana M; Devos, Damien P (2020-07-01). Ursula Battistuzzi, Fabia (ed.). "Origin and Evolution of Polycyclic Triterpene Synthesis". Molecular Biology and Evolution. 37 (7): 1925–1941. doi:10.1093/molbev/msaa054. ISSN 0737-4038. PMC 7306690. PMID 32125435.
- ^ Pan, Jian-Jung; Solbiati, Jose O.; Ramamoorthy, Gurusankar; Hillerich, Brandan S.; Seidel, Ronald D.; Cronan, John E.; Almo, Steven C.; Poulter, C. Dale (2015-05-27). "Biosynthesis of Squalene from Farnesyl Diphosphate in Bacteria: Three Steps Catalyzed by Three Enzymes". ACS Central Science. 1 (2): 77–82. doi:10.1021/acscentsci.5b00115. ISSN 2374-7943. PMC 4527182. PMID 26258173.
- ^ Misawa, Norihiko (2010-01-01), Liu, Hung-Wen (Ben); Mander, Lew (eds.), "1.20 - Carotenoids", Comprehensive Natural Products II, Oxford: Elsevier, pp. 733–753, doi:10.1016/b978-008045382-8.00009-5, ISBN 978-0-08-045382-8, retrieved 2021-10-22
