Discovery of Geranylgeranyl Pyrophosphate Synthase (GGPPS) Paralogs from Haematococcus pluvialis Based on Iso-Seq Analysis and Their Function on Astaxanthin Biosynthesis

被引:15
|
作者
Huang, Danqiong [1 ,2 ]
Liu, Wenfu [1 ]
Li, Anguo [1 ]
Wang, Chaogang [1 ]
Hu, Zhangli [1 ]
机构
[1] Shenzhen Univ, Shenzhen Key Lab Marine Bioresource & Ecoenvironm, Shenzhen Engn Lab Marine Algal Biotechnol, Coll Life Sci & Oceanog,Guangdong Prov Key Lab Pl, Shenzhen 518060, Peoples R China
[2] Shenzhen Univ, Coll Optoelect Engn, Minist Educ & Guangdong Prov, Key Lab Optoelect Devices & Syst, Shenzhen 518060, Peoples R China
基金
中国国家自然科学基金;
关键词
GGPPS; Haematococcus pluvialis; astaxanthin; Iso-Seq; DIFFERENTIAL EXPRESSION; ISOPRENOID BIOSYNTHESIS; ESCHERICHIA-COLI; BETA-CAROTENE; DIPHOSPHATE; GENES; PATHWAY; IDENTIFICATION; MICROALGAE; MECHANISM;
D O I
10.3390/md17120696
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Haematococcus pluvialis is widely distributed in the world and well known as the richest natural source of astaxanthin that is a strong antioxidant with excellent commercial value. The pathway of astaxanthin biosynthesis in H. pluvialis has been documented as an enzymatic reaction. Several enzymes have been reported, but their isoforms or homologs have not been investigated genome-wide. To better understand the astaxanthin biosynthesis pathway in H. pluvialis, eight candidates of the geranylgeranyl pyrophosphate synthase gene (HpGGPPS) predicted from Iso-seq data were isolated in this study. The length of coding region of these candidates varied from 960 bp to 1272 bp, composing of 7-9 exons. The putative amino acids of all candidates composed the signature domain of GGPPS gene. However, the motifs in the domain region are varied, indicating different bio-functions. Phylogenetic analysis revealed eight candidates can be clustered into three groups. Only two candidates in Group1 encode the synthase participating in the astaxanthin formation. The yield of astaxanthin from these two candidates, 7.1 mg/g (DW) and 6.5 mg/g (DW) respectively, is significant higher than that from CrtE (2.4 mg/g DW), a GGPPS gene from Pantoea ananatis. This study provides a potential productive pathway for astaxanthin synthesis.
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页数:14
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