Biology:CRT (genetics)
CRT is the gene cluster responsible for the biosynthesis of carotenoids. Those genes are found in eubacteria,[1] in algae[2] and are cryptic in Streptomyces griseus.[3]
Role of CRT genes in carotenoid biosynthesis
The CRT gene cluster consists of twenty-five genes such as crtA, crtB, crtC, crtD, crtE, crtF, crtG, crtH, crtI, crtO, crtP, crtR, crtT, crtU, crtV, and crtY, crtZ. These genes play a role in varying stages of the Astaxanthin biosynthesis and Carotenoid biosynthesis (Table 1).[4]
crtE encodes for an enzyme known as geranylgeranyl diphosphate synthase known to catalyze the condensation reaction of isopentenyl pyrophosphate (IPP) and dimethylallyl pyrophosphate (DMAPP) into geranylgeranyl diphosphate (GGDP).[5][6] Two GGDP molecules are subsequently converted into a single phytoene molecule by phytoene synthase, an enzyme encoded by crtB, known as PSY in Chlorophyta.[2][5][6] The following desaturation of phytoene into ζ-carotene is catalyzed by the phytoene desaturase encoded by crtI, crtP, and/or PDS.[2][5][6] ζ -carotene can also be obtained through phytoene using the carotene 2,4-desaturase enzyme (crtD).[2][7] Depending on the species, varying carotenoids are accumulated following these steps.[1][8]
Spirilloxanthin
Spirilloxanthin is obtained from lycopene following a hydration, desaturation, and methylation reaction. These reactions are catalyzed by carotene hydratase (crtC), carotene 3,4- desaturase (crtD), and carotene methyltransferase (crtF), respectively.[6][1]
Canthaxanthin
Lycopene is cyclized through two enzymes lycopene cyclase and β-C-4-oxygenase/β-carotene ketolase encoded on the crtY (in Chlorophyta) /crtL (in cyanobacteria), and crtW, respectively. crtY cyclizes lycopene into β-carotene, which is subsequently oxygenated by crtW to form canthaxanthin.[6]
Zeaxanthin and lutein
Zeaxanthin and lutein are obtained through hydroxylation of α- and β-carotene.[1] Hydroxylation of Zeaxanthin occurs by β-carotene hydroxylase an enzyme encoded on the crtR (in cyanobacteria) and crtZ gene (in Chlorophyta).[6]
Other
Zeaxanthin can be further processed to obtain zeaxanthin-diglucoside by Zeaxanthin glucosyl transferase (crtX).
Echinenone is obtained from β -carotene through the catalyzing enzyme β-C-4-oxygenase/β-carotene ketolase (crtO).[9] CrtO, also known as bkt2 in Chlorophyta, is also involved in the conversion of other carotenoids into Canthaxanthin, 3-Hydroxyechinenone, 3'-Hydroxyechinenone, Adonixanthin, and Astaxanthin.[9][10]CrtZ, similarly to crtO, is also capable of converting carotenoids into β-cryptoxanthin, Zeaxanthin, 3-Hydroxyechinenone, 3'-Hydroxyechinenone, Astaxanthin, Adonixanthin, and Adonirubin.[9]
crtH catalyzes the isomerization of cis-carotenes into trans-carotenes through carotenoid isomerase.[2]
crtG encodes for carotenoid 2,2'- β-hydroxylase, this enzyme leads to the formation of 2-hydroxylated and 2,2′-dihydroxylated products in E coli.[11]
| Gene | Enzyme | Catalyzed reaction |
|---|---|---|
| crtE | GGDP synthase | IPP and DMAPP conversion to GGDP |
| crtB (PSY*) | Phytoene Synthase | GGDP conversion to phytoene |
| crtP (PDS*) | Phytoene desaturase | Conversion of phytoene into ζ- carotene |
| crtI | Phytoeine desaturase | Conversion of phytoene into ζ- carotene |
| crtQ | ζ- carotene desaturase | Desaturation of ζ- carotene to lycopene |
| crtH | Carotenoid isomerase | Isomeration of cis to trans carotones |
| crtY (lcy-E) | Lycopene cyclase | Cyclization of lycopene |
| crtL (lcy-B) | Lycopene cyclase | Cyclization of lycopene |
| crtD | Carotene 3,4-desaturase | Conversion of phytoene to ζ-carotene |
| crtA | Spheroidene monooxygenase | Conversion of spheroidene to spheroidenone |
| crtR+ | β-carotene hydroxylase (various Cyanobacteria) | Hydroxylation of β-carotene to zeaxanthin |
| crtZ* | β-carotene hydroxylase (various Chlorophyta) | Hydroxylation of β-carotene to zeaxanthin |
| crtX | Zeaxanthin glucosyl transferase | Conversion of zeaxanthin to zeaxanthin-diglucoside |
| crtW (bkt2*) | β-C-4-oxygenase/β-carotene ketolase | Conversion of β-carotene to canthaxanthin |
| crtO | β-C-4-oxygenase/β-carotene ketolase | Conversion of β-carotene to echinenone |
| crtC | Carotene hydratase | Conversion of neurosporene to demethylspheroidene and lycopene to hydroxy derivatives |
| crtG | Carotenoid 2,2′-β-hydroxylase | Conversion of myxol to 2-hydroxymyxol and zeaxanthin to nostoxanthin |
| crtK | Carotenoid regulation | - |
| * In Chlorophyta, + In cyanobacteria | ||
Phylogeny
Previous studies have indicated through phylogenetic analysis that evolutionary patterns of crt genes are characterized by horizontal gene transfer and gene duplication events.[12]
Horizontal gene transfer has been hypothesized to have occurred between cyanobacteria and Chlorophyta, as similarities in these genes have been found across taxa.[12] Note, however, that some cyanobacteria retained their nature. Horizontal gene transfer among species occurred with a high probability in genes involved in the initial steps of the carotenoid biosynthesis pathway such as crtE, crtB, crtY, crtL, PSY, and crtQ. These genes are often well conserved while others involved in the later stages of Carotenoid biosynthesis such as crtW and crtO are less conserved.[1] The less conserved nature of these genes allowed for the expansion of the carotenoid biosynthesis pathway and its end products. Amino acid variations within crt genes have evolved due to purifying and adaptive selection.[2]
Gene duplications are suspected to have occurred due to the presence of multiple copies of ctr clusters or genes within a single species.[2] An example of this can be seen in the Bradyrhizobium ORS278 strain, where initial crt genes can be found (excluding crtC, crtD, and crtF genes) as well as a second crt gene cluster. This second gene cluster has been shown to also be involved in carotenoid biosynthesis using its crt paralogs.[6][13]
References
- ↑ 1.0 1.1 1.2 1.3 1.4 Carotenoid biosynthetic pathway: molecular phylogenies and evolutionary behavior of crt genes in eubacteria. Phadwal K, Gene, 17 January 2005, volume 345, issue 1, pages 35-43, PMID 15716108
- ↑ 2.0 2.1 2.2 2.3 2.4 2.5 2.6 2.7 Molecular phylogenies and evolution of crt genes in algae. Chen Q, Jiang JG and Wang F, Crit Rev Biotechnol., Apr-Jun 2007;, volume 27, issue 2, pages 77-91, PMID 17578704
- ↑ Activation and analysis of cryptic crt genes for carotenoid biosynthesis from Streptomyces griseus. Schumann G1, Nürnberger H, Sandmann G and Krügel H, Mol Gen Genet., 28 October 1996, volume 252, issue 6, pages 658-666, PMID 8917308
- ↑ Nishida, Yasuhiro; Adachi, Kyoko; Kasai, Hiroaki; Shizuri, Yoshikazu; Shindo, Kazutoshi; Sawabe, Akiyoshi; Komemushi, Sadao; Miki, Wataru et al. (August 2005). "Elucidation of a Carotenoid Biosynthesis Gene Cluster Encoding a Novel Enzyme, 2,2′-β-Hydroxylase, from Brevundimonas sp. Strain SD212 and Combinatorial Biosynthesis of New or Rare Xanthophylls". Applied and Environmental Microbiology 71 (8): 4286–4296. doi:10.1128/AEM.71.8.4286-4296.2005. ISSN 0099-2240. PMID 16085816. Bibcode: 2005ApEnM..71.4286N.
- ↑ 5.0 5.1 5.2 Sandmann, Gerhard; Misawa, Norihiko (January 1992). "New functional assignment of the carotenogenic genescrtBandcrtEwith constructs of these genes fromErwiniaspecies". FEMS Microbiology Letters 90 (3): 253–258. doi:10.1111/j.1574-6968.1992.tb05162.x. ISSN 0378-1097.
- ↑ 6.0 6.1 6.2 6.3 6.4 6.5 6.6 Giraud, Eric; Hannibal, Laure; Fardoux, Joël; Jaubert, Marianne; Jourand, Philippe; Dreyfus, Bernard; Sturgis, James N.; Verméglio, Andre (April 2004). "Two Distinct crt Gene Clusters for Two Different Functional Classes of Carotenoid in Bradyrhizobium". Journal of Biological Chemistry 279 (15): 15076–15083. doi:10.1074/jbc.m312113200. ISSN 0021-9258. PMID 14734565.
- ↑ Yang, Ying; Yatsunami, Rie; Ando, Ai; Miyoko, Nobuhiro; Fukui, Toshiaki; Takaichi, Shinichi; Nakamura, Satoshi (2015-02-23). "Complete Biosynthetic Pathway of the C50Carotenoid Bacterioruberin from Lycopene in the Extremely Halophilic Archaeon Haloarcula japonica". Journal of Bacteriology 197 (9): 1614–1623. doi:10.1128/jb.02523-14. ISSN 0021-9193. PMID 25712483. PMC 4403650. http://dx.doi.org/10.1128/jb.02523-14.
- ↑ Maoka, Takashi (2019-10-01). "Carotenoids as natural functional pigments". Journal of Natural Medicines 74 (1): 1–16. doi:10.1007/s11418-019-01364-x. ISSN 1340-3443. PMID 31588965. PMC 6949322. http://dx.doi.org/10.1007/s11418-019-01364-x.
- ↑ 9.0 9.1 9.2 Harker, Mark; Hirschberg, Joseph (1997-03-10). "Biosynthesis of ketocarotenoids in transgenic cyanobacteria expressing the algal gene for β-C-4-oxygenase, crtO". FEBS Letters 404 (2–3): 129–134. doi:10.1016/s0014-5793(97)00110-5. ISSN 0014-5793. PMID 9119049. http://dx.doi.org/10.1016/s0014-5793(97)00110-5.
- ↑ Fernández-González, Blanca; Sandmann, Gerhard; Vioque, Agustín (April 1997). "A New Type of Asymmetrically Acting β-Carotene Ketolase Is Required for the Synthesis of Echinenone in the Cyanobacterium Synechocystis sp. PCC 6803". Journal of Biological Chemistry 272 (15): 9728–9733. doi:10.1074/jbc.272.15.9728. ISSN 0021-9258. PMID 9092504.
- ↑ Nishida, Yasuhiro; Adachi, Kyoko; Kasai, Hiroaki; Shizuri, Yoshikazu; Shindo, Kazutoshi; Sawabe, Akiyoshi; Komemushi, Sadao; Miki, Wataru et al. (August 2005). "Elucidation of a Carotenoid Biosynthesis Gene Cluster Encoding a Novel Enzyme, 2,2′-β-Hydroxylase, from Brevundimonas sp. Strain SD212 and Combinatorial Biosynthesis of New or Rare Xanthophylls". Applied and Environmental Microbiology 71 (8): 4286–4296. doi:10.1128/aem.71.8.4286-4296.2005. ISSN 0099-2240. PMID 16085816. PMC 1183362. Bibcode: 2005ApEnM..71.4286N. http://dx.doi.org/10.1128/aem.71.8.4286-4296.2005.
- ↑ 12.0 12.1 Phadwal, Kanchan (January 2005). "Carotenoid biosynthetic pathway: molecular phylogenies and evolutionary behavior of crt genes in eubacteria". Gene 345 (1): 35–43. doi:10.1016/j.gene.2004.11.038. ISSN 0378-1119. PMID 15716108. http://dx.doi.org/10.1016/j.gene.2004.11.038.
- ↑ Tran, Duc; Haven, James; Qiu, Wei-Gang; Polle, Juergen E. W. (2008-12-09). "An update on carotenoid biosynthesis in algae: phylogenetic evidence for the existence of two classes of phytoene synthase". Planta 229 (3): 723–729. doi:10.1007/s00425-008-0866-2. ISSN 0032-0935. PMID 19066941. PMC 6008256. http://dx.doi.org/10.1007/s00425-008-0866-2.
 |  |
