4.7 Article

Characterization and Functional Identification of a Gene Encoding Geranylgeranyl Diphosphate Synthase from Dunaliella bardawil

期刊

JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
卷 63, 期 35, 页码 7805-7812

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jafc.5b02732

关键词

Dunaliella bardawil; geranylgeranyl diphosphate synthase (geranylgeranyl pyrophosphate synthase); functional expression; carotenoids

资金

  1. National Natural Foundation of China [31171631, 31571773]
  2. Key Natural Science Foundation of Guangdong Province, China [2014A030311020]
  3. Guangdong Province Science and Technology Plan, China [2011B031200005, 2013B010404009]
  4. Guangdong Provincial Bureau of Ocean and Fishery Science and Technology, China [A201301C04]

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Geranylgeranyl diphosphate synthase (GGPS) catalyzes the biosynthesis of geranylgeranyl diphosphate, a key precursor for carotenoid biosynthesis. In this study, a full-length cDNA encoding GGPS from Dunaliella bardawil (DbGGPS) was isolated by rapid amplification of cDNA ends (RACE) for the first time. The full-length cDNA of DbGGPS was 1814 bp, containing a 1074 bp ORF encoding 357 amino acids with a calculated mass of 38.88 kDa. Analysis of DbGGPS genomic DNA revealed that it contained 10 exons and 9 introns. It was predicted that DbGGPS possessed a 48 amino acid transit peptide at its N terminus. Bioinformatic analysis revealed that DbGGPS was a member of a group of polyprenyltransferases with five conserved domains and two highly conserved aspartate-rich motifs. Using heterologous expression, carotenoid complementation assay, and gene deletion analysis, it was shown that the coding region of DbGGPS encodes a functional GGPS. This provides new gene sources for carotenoid genetic engineering.

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