Geranyl diphosphate synthase from Abies grandis: cDNA isolation, functional expression, and characterization

2002 ◽  
Vol 405 (1) ◽  
pp. 130-136 ◽  
Author(s):  
Charles Burke ◽  
Rodney Croteau
2004 ◽  
Vol 27 (12) ◽  
pp. 1979-1985 ◽  
Author(s):  
Madoka Hosoi ◽  
Michiho Ito ◽  
Toru Yagura ◽  
Robert Phillip Adams ◽  
Gisho Honda

2021 ◽  
Vol 20 (1) ◽  
Author(s):  
Xiaomin Wu ◽  
Guang Ma ◽  
Chuanyang Liu ◽  
Xin-yuan Qiu ◽  
Lu Min ◽  
...  

Abstract Background Pinene is a monoterpene, that is used in the manufacture of fragrances, insecticide, fine chemicals, and renewable fuels. Production of pinene by metabolic-engineered microorganisms is a sustainable method. Purple non-sulfur photosynthetic bacteria belong to photosynthetic chassis that are widely used to synthesize natural chemicals. To date, researches on the synthesis of pinene by purple non-sulfur photosynthetic bacteria has not been reported, leaving the potential of purple non-sulfur photosynthetic bacteria synthesizing pinene unexplored. Results Rhodobacter sphaeroides strain was applied as a model and engineered to express the fusion protein of heterologous geranyl diphosphate synthase (GPPS) and pinene synthase (PS), hence achieving pinene production. The reaction condition of pinene production was optimized and 97.51 μg/L of pinene was yielded. Then, genes of 1-deoxy-d-xylulose 5-phosphate synthase, 1-deoxy-d-xylulose 5-phosphate reductoisomerase and isopentenyl diphosphate isomerase were overexpressed, and the ribosome binding site of GPPS-PS mRNA was optimized, improving pinene titer to 539.84 μg/L. Conclusions In this paper, through heterologous expression of GPPS-PS, pinene was successfully produced in R. sphaeroides, and pinene production was greatly improved by optimizing the expression of key enzymes. This is the first report on pinene produce by purple non-sulfur photosynthetic bacteria, which expands the availability of photosynthetic chassis for pinene production.


2008 ◽  
Vol 55 (5) ◽  
pp. 719-733 ◽  
Author(s):  
Yu-Yun Hsiao ◽  
Mei-Fen Jeng ◽  
Wen-Chieh Tsai ◽  
Yu-Chen Chuang ◽  
Chia-Ying Li ◽  
...  

2007 ◽  
Vol 52 (4) ◽  
pp. 752-762 ◽  
Author(s):  
Chris C. N. Van Schie ◽  
Kai Ament ◽  
Axel Schmidt ◽  
Theo Lange ◽  
Michel A. Haring ◽  
...  

2020 ◽  
Vol 182 (4) ◽  
pp. 1933-1945 ◽  
Author(s):  
Hayato Ueoka ◽  
Kanako Sasaki ◽  
Tatsuya Miyawaki ◽  
Takuji Ichino ◽  
Kanade Tatsumi ◽  
...  

Plants ◽  
2020 ◽  
Vol 9 (5) ◽  
pp. 666
Author(s):  
Hafiz Muhammad Kamran ◽  
Syed Bilal Hussain ◽  
Shang Junzhong ◽  
Lin Xiang ◽  
Long-Qing Chen

Geranyl diphosphate synthase (GPPS) is a plastid localized enzyme that catalyzes the biosynthesis of Geranyl diphosphate (GPP), which is a universal precursor of monoterpenes. Wintersweet (Chimonanthus praecox L.), a famous deciduous flowering shrub with a strong floral scent character, could have GPPS-like homologs that are involved in monoterpenes biosynthesis, but it remains unclear. In the present study, five full-length GPPS and geranylgeranyl diphosphate synthases (GGPPS) genes were identified in the wintersweet transcriptome database. The isolated cDNAs showed high protein sequence similarity with the other plants GPPS and GGPPS. The phylogenetic analysis further classified these cDNAs into four distinct clades, representing heterodimeric GPPS small subunits (SSU1 and SSU2), homodimeric GPPS, and GGPPS. Analysis of temporal expression revealed that all genes have the highest transcript level at the full-open flower stage. From tissue-specific expression analysis, CpGPPS.SSU1 and CpGGPPS1 were predominantly expressed in petal and flower, whereas CpGPPS.SSU2, GPPS, and GGPPS2 showed a constitutive expression. Additionally, the subcellular localization assay identified the chloroplast localization of SSUs and GGPPSs proteins, and the yeast two-hybrid assay showed that both CpGPPS.SSU1 and CpGPPS.SSU2 can interact with the GGPPS proteins. Taken together, these preliminary results suggest that the heterodimeric GPPS can regulate floral scent biosynthesis in wintersweet flower.


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