Cloning and Functional Expression of Ζ-Carotene Desaturase, A Novel Carotenoid Biosynthesis Gene From Ficus Carica

González Villa T, Araya

Abstract

 Carotene desaturation, an essential step in the carotenoid biosynthesis pathway, is catalyzed by two enzymes, phytoene desaturase (PDS) and ζ-carotene desaturase (zeta carotene desaturase, ZDS). Here we describe cloning and E. coli expression of zdsfc, a novel Ficus carica ζ-carotene desaturase catalyzing dehydrogenation of ζ-carotene into neurosporene and finally lycopene. The ζ-carotene desaturase (ZDS) gene was amplified from the fig tree  by rapid amplification of cDNA ends (RACE) and spanned a 1746 bp open reading frame (ORF), encoding a protein of 582 amino acid residues with a predicted molecular weight of 64kD. The N-terminal region of this polypeptide contained a putative transit sequence for plastid targeting. By phylogenetic and sequence analyses, zdsfc showed high homology with previously described ζ-carotene desaturases from higher plant species [1-4]. Additionally, sequence analysis revealed a high degree of conservation among plant ZDSs. The deduced ZDS protein, designated zdsfc, also contains an N-terminus dinucleotide-binding, followed by a conserved region identified in other carotene desaturase sequences. These data, taken together, confirm our cloned zdsfc as an integral part of the ZDS family of proteins.

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