Skip to main content
Log in

Glucosylation of the saffron apocarotenoid crocetin by a glucosyltransferase isolated from Crocus sativus stigmas

  • Original Article
  • Published:
Planta Aims and scope Submit manuscript

Abstract

Saffron, the dry stigma of Crocus sativus L., is considered to be the world’s most expensive spice. Three major apocarotenoids—crocin, crocetin and picrocrocin—are responsible for the colour and bitter taste of saffron. The final step in the biosynthesis of the 20-carbon esterified carotenoid crocin is the transformation of the insoluble crocetin into a soluble and stable storage form by glucosylation. These glucosylation reactions are catalysed by glucosyltransferases (GTases) that play a crucial role in natural-product biosynthesis. Using degenerate primers designed to match the plant secondary product GTase (PSPG) box we cloned two cDNAs, UGTCs2 and UGTCs3, from C. sativus stigmas that encode putative polypeptides of 460 and 475 amino acids, respectively. These genes were expressed differentially in saffron tissues. UGTCs2 was mainly expressed in fully developed stigmas, whereas UGTCs3 was mainly expressed in stamens. The UGTCs2 transcript was not detected in the stigma tissue of a Crocus species that does not synthesize crocin, while UGTCs3 and other structural genes for carotenoid biosynthesis were expressed in the stigma of all tested Crocus species. To identify the biochemical function of UGTCs2, the isolated cDNA was expressed in Escherichia coli cells. The recombinant protein UGTCs2 had glucosylation activity against crocetin, crocetin β-d-glucosyl ester and crocetin β-d-gentibiosyl ester. These results might suggest that the isolated clone UGTCs2 codes for a saffron crocetin GTase.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1a, b
Fig. 2a, b
Fig. 3a–d
Fig. 4
Fig. 5a–c
Fig. 6a, b

Similar content being viewed by others

Abbreviations

ABA :

Abscisic acid

BCH :

β-Carotene hydroxylase

IAA :

Indole acetic acid

GA 3 :

Gibberellic acid

GTase :

Glucosyltransferase

JA :

Jasmonic acid

PSY :

Phytoene synthase

RACE :

Rapid amplification of cDNA ends

SA :

Salicylic acid

UGT :

UDP-glucosyl transferase

References

  • Abdullaev FI (2002) Cancer chemopreventive and tumoricidal properties of saffron (Crocus sativus). Exp Biol Med 227:20–25

    CAS  Google Scholar 

  • Alonso GL, Salinas MR, Garijo J (1998) Method to determine the authenticity of aroma of saffron (Crocus sativus L). J Food Prot 61:1525–1528

    CAS  PubMed  Google Scholar 

  • Bowles DJ (1998) A novel tomato gene that rapidly responds to wound- and pathogen-related signals. Plant J 14:137–142

    Article  CAS  Google Scholar 

  • Boss PK, Davies C, Robinson SP (1996) Expression of anthocyanin biosynthesis pathway genes in red and white grapes. Plant Mol Biol 32:565–569

    CAS  PubMed  Google Scholar 

  • Bouvier F, Suire C, Mutterer J, Camara B (2003) Oxidative remodeling of chromoplast carotenoids: identification of the carotenoid dioxygenase CsCCD and CsZCD genes involved in Crocus secondary metabolite biogenesis. Plant Cell 15:47–62

    Article  CAS  PubMed  Google Scholar 

  • Church GM, Gilbert W (1984) Genomic sequencing. Proc Natl Acad Sci USA 81:1991–1995

    CAS  PubMed  Google Scholar 

  • Cormier F, Dufresne C, Dorion S (1995) Enhanced crocetin glucosylation by means of maltosyl-β-cyclodextrin encapsulation. Biotechnol Tech 9:553–556

    CAS  Google Scholar 

  • Côté F, Cormier F, Dufresne C, Willemot C (2000) Properties of a glucosyltransferase involved in crocin synthesis. Plant Sci 153:55–63

    Article  Google Scholar 

  • Dixon SC, Martin RC, Mok MC, Shaw G, Mok DWS (1989) Zeatin glycosylation enzymes in Phaseolus. Isolation of O-glucosyltransferase from P. lunatus and comparison to O-xylosyltransferase from P. vulgaris. Plant Physiol 90:1316–1321

    CAS  Google Scholar 

  • Doyle JJ, Doyle LH (1990) Isolation of plant DNA from fresh tissue. Focus 12:13–15

    Google Scholar 

  • Dufresne C, Cormier F, Dorion S (1997) In vitro formation of crocetin glucosyl esters by Crocus sativus callus extract. Planta Med 63:150–153

    CAS  PubMed  Google Scholar 

  • Dufresne C, Cormier F, Dorion S, Niggli UA, Pfister S, Pfander H (1999) Glycosylation of encapsulated crocetin by a Crocus sativus L. cell culture. Enzyme Microbial Technol 24:453–462

    Article  CAS  Google Scholar 

  • Eugster CH, Hurlimann H, Leuenberger HJ (1969) Crocetindyaldehyd und crocetinhaldaldehyb als blutenfarbstoffe von Jacquinia angustifolia. Helv Chim Acta 52:89–90

    Google Scholar 

  • Ford CM, Boss P, Hoj PB (1998) Cloning and characterization of Vitis vitifera UDP-glucose:flavonoid 3-O-glucosyltransferase, a homologue of enzyme encoded by the maize Bronze-1 locus that may primarily serve to glucosylate anthocyanidins in vivo. J Biol Chem 273:9224–9233

    Article  CAS  PubMed  Google Scholar 

  • Gopalakrishna R, Kumar G, Prasad BT, Mathew MK, Kumar M (2001) A stress-responsive gene from groundnut, Gdi-15, is homologous to flavonol 3-O-glucosyltransferase involved in anthocyanin biosynthesis. Biochem Biophys Res Commun 284:574–579

    Article  CAS  PubMed  Google Scholar 

  • Himeno H, Sano K (1987) Synthesis of crocin, picrocrocin and safranal by saffron stigma-like structures proliferated in vitro. Agric Biol Chem 51:2395–2400

    CAS  Google Scholar 

  • Horvath D, Chua NH (1996) Identification of an immediate-early salicylic acid-inducible tobacco gene and characterization of induction by other compounds. Plant Mol Biol 31:1061–1072

    CAS  PubMed  Google Scholar 

  • Hosseinzadeh H, Younesi HM (2002) Antinociceptive and anti-inflammatory effects of Crocus sativus L. stigma and petal extracts in mice. BMC Pharmacol 2:7–14

    Article  PubMed  Google Scholar 

  • Hughes J, Hughes MA (1994) Multiple secondary plant product UDP-glucose glucosyltransferase genes expressed in cassava (Manihot esculenta Crantz) cotyledons. DNA Seq 5:41–49

    CAS  PubMed  Google Scholar 

  • Imanishi S, Hashizume K, Kojima H, Ichihara A, Nakamura K (1998) An mRNA of tobacco cell, which is rapidly inducible by methyl jasmonate in the presence of cycloheximide, codes for a putative glycosyltransferase. Plant Cell Physiol 39:202–211

    CAS  PubMed  Google Scholar 

  • Jones PR, Møller BL, Høj PB (1999) The UDP-glucose:p-hydroxy-mandelonitrile-O-glucosyltransferase that catalyses the last step in synthesis of the cyanogenic glucoside dhurrin in Sorghum bicolor. J Biol Chem 274:35483–35491

    Article  CAS  PubMed  Google Scholar 

  • Laemmli UK (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227:680–685

    PubMed  Google Scholar 

  • Lee H-I, Raskin I (1999) Purification, cloning, and expression of a pathogen inducible UDP-glucose: salicylic acid glucosyltransferase from tobacco. J Biol Chem 274:36637–36642

    Article  CAS  PubMed  Google Scholar 

  • Li Y, Baldauf S, Lim E-K, Bowles D (2001) Phylogenetic analysis of the UDP-glycosyltransferase multigene family of Arabidopsis thaliana. J Biol Chem 276:4338–4343

    Article  CAS  PubMed  Google Scholar 

  • Liao YH, Houghton PJ, Hoult JR (1999) Novel and known constituents from Buddleja species and their activity against leukocyte eicosanoid generation. J Nat Prod 62:1241–1245

    Article  CAS  PubMed  Google Scholar 

  • Lim EK, Li Y, Parr A, Jackson R, Ashford DA, Bowles DJ (2001) Identification of glucosyltransferase genes involved in sinapate metabolism and lignin synthesis in Arabidopsis. J Biol Chem 276:4344–4349

    Article  CAS  PubMed  Google Scholar 

  • Lim E-K, Doucet CJ, Li Y, Elias L, Worrall D, Spencer SP, Ross J, Bowles DJ (2002) The activity of Arabidopsis glycosyltransferases toward salicylic acid, 4-hydroxybenzoic acid, and other benzoates. J Biol Biochem 277:586–592

    CAS  Google Scholar 

  • Lim E-K, Baldauf S, Li Y, Elias L, Worrall D, Spencer SP, Jackson, RG, Taguchi G, Ross J, Bowles DJ (2003) Evolution of substrate recognition across a multigene family of glycosyltransferases in Arabidopsis. Glycobiology 13:139–145

    Article  CAS  PubMed  Google Scholar 

  • Miller KD, Guyon V, Evans JN, Shuttleworth WA, Taylor LP (1999) Purification, cloning, and heterologous expression of a catalytically efficient flavonol 3-O-galactosyltransferase expressed in the male gametophyte of Petunia hybrida. J Biol Chem 274:34011–34019

    Article  CAS  PubMed  Google Scholar 

  • Pfander H (1976) carotenoid glycosides. Pure Appl Chem 47:121–128

    CAS  Google Scholar 

  • Pfander H, Wittwer F (1975) Carotinoid-glykoside. Unterguchungen zur carotinoids zusammensetzung im safran. Helv Chim Acta 58:1608–1620

    CAS  PubMed  Google Scholar 

  • Pfander H, Wittwer F (1979) Carotinoid-Glycosylester (3. Mitteilung). Die Synthese von Crocetin-di-(beta-d-glucosyl)-ester. Eine neue Methode zur selektiven Veresterung von ungeschützter beta-d-Glucose. Helv Chim Acta 62:1944–1951

    CAS  Google Scholar 

  • Pfander H, Schurtenberger H (1982) Biosynthesis of C20-carotenoids in Crocus sativus. Phytochemistry 21:1039–1042

    Article  CAS  Google Scholar 

  • Pfister S, Meyer P, Steck A, Pfander H (1996) Isolation and structure elucidation of carotenoid glycoslyesters on gardenia fruits (Gardenia jasminoides) and saffron (Crocus sativus) J Agric Food Chem 44:2612–2615

    Google Scholar 

  • Rea PA (1999) MRP subfamily ABC transporters from plant and yeast. J Exp Bot 50:895–913

    CAS  Google Scholar 

  • Ross J, Li Y, Lim E, Bowles DJ (2001) Higher plant glycosyltransferases. Genome Biol 2:3004.1–3004.6

    Article  Google Scholar 

  • Rychener M, Bigler P, Pfander H (1984) Isolation and structure elucidation of neapolitanose (O-β-d-glucopyranosyl-(1→2)-O-[β-d-glucopyranosyl-(1→6)[-d-glucose), a new trisaccharide from the stigmas of garden crocuses (Crocus neapolitanus var.) Helv Chim Acta 67:386–556

  • Song C (1991) Chemical constituents of saffron (Crocus sativus) II. The flavonol compounds of petals. Chem Abstr 114:214–242

    Google Scholar 

  • Straubinger M, Jezussek M, Waibel R, Winterhalter P (1997) Novel glycosidic constituents of saffron. J Agric Food Chem 45:1678–1681

    CAS  Google Scholar 

  • Szerszen JB, Szczyglowski K, Bandurski RS (1994) Iaglu, a gene from Zea mays involved in conjugation of growth hormone indole-3-acetic acid. Science 265:1699–1701

    CAS  PubMed  Google Scholar 

  • Tandon JS, Katti SB, Ruedi P, Eugster CH (1979) Crocetin-dialdehyde from Coleus forskohlii Briq., labiatae. Helv Chim Acta 274:2706–2707

    Google Scholar 

  • Tarantilis PA, Polissiou, M (1997) Isolation and identification of the aroma constituents of saffron (Crocus sativa). J Agric Food Chem 45:459–462

    Article  CAS  Google Scholar 

  • Tarantilis PA, Tsoupras G, Polissiou M (1995) Determination of saffron (Crocus sativus L.) components in crude plant extract using high-performance liquid chromatography-UV-visible photodiode-array detection-mass spectrometry. J Chromatogr 699:107–118

    Article  CAS  PubMed  Google Scholar 

  • Thompson JD, Higgins DG, Gibson TJ (1994) CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res 22:4573–4680

    Google Scholar 

  • Vogt T, Jones P (2000) Glycosyltransferases in plant natural product synthesis: characterization of a supergene family. Trends Plant Sci 5:380–386

    Article  CAS  PubMed  Google Scholar 

  • Vogt T, Taylor LP (1995) Flavonol 3-O-glycosyltransferases associated with petunia pollen produce gametophyte-specific flavonol diglycosides. Plant Physiol 108:903–911

    Article  CAS  PubMed  Google Scholar 

  • Verma SK, Bordia A (1998) Antioxidant property of saffron in man. Indian J Med Sci 52:205–207

    CAS  PubMed  Google Scholar 

  • Wierman R, Vieth K (1983) Outer pollen wall, an important accumulation site for flavonoids. Protoplasma 118:230–233

    Google Scholar 

  • Winterhalter P, Rouseff RS, eds (2001) Carotenoid-derived aroma compounds: an introduction. In: Carotenoid-derived aroma compounds. American Chemical Society, Washington, DC, pp 1–17

  • Winterhalter P, Skouroumounis GK (1997) Glycoconjugated aroma compounds: occurrence, role and biotechnological transformation. Adv Biochem Eng Biotechnol 55:73–105

    CAS  PubMed  Google Scholar 

  • Yamazaki M, Gong Z, Fukichi-Mizutani, M, Fukui Y, Tanaka Y, Kusumi T, Saito K (1999) Molecular cloning and biochemical characterization of a novel anthocyanin 5-O-glucosyltransferase by mRNA differential display for plant forms regarding anthocyanin. J Biol Chem 274:7405–7411

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

We gratefully acknowledge the contribution of R. Castillo in the collection and preparation of some RNA samples. We thank Drs. A. Gómez and D. Lunt (Hull University, UK) for critical reading of the manuscript and corrections; the Biochemistry Department of Valencia University (Spain) for radiation laboratory facilities; and Drs. N. Kayali (Universidad Complutense de Madrid, Spain) and O. Jauregui (Barcelona University, Spain) for the mass spectra facilities and analysis. This research was supported by Consejería de Ciencia y Tecnología de la JCCM grant No. PAI-02-026 and MCyT grant BIO2003-05259.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Lourdes Gómez-Gómez.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Moraga, A.R., Nohales, P.F., Pérez, J.A.F. et al. Glucosylation of the saffron apocarotenoid crocetin by a glucosyltransferase isolated from Crocus sativus stigmas. Planta 219, 955–966 (2004). https://doi.org/10.1007/s00425-004-1299-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00425-004-1299-1

Keywords

Navigation