Fusion constructs as protein overexpression vectors proved to be critical in the heterologous expression of terpene synthases in cyanobacteria. The concept was recently applied to the heterologous overexpression of the beta-phellandrene synthase (beta-PHLS) from plants, fused to the highly expressed endogenous cpcB gene encoding the beta-subunit of phycocyanin. Overexpressed CpcB*PHLS fusion proteins enhanced the heterologous yield of C10H16 beta-phellandrene hydrocarbons production in Synechocystis. This work extended the concept of fusion constructs as protein overexpression vectors by showing that highly expressed heterologous genes could also serve as leader sequences for protein overexpression in cyanobacteria. Examined are the kanamycin nptI and chloramphenicol cmR resistance cassettes, both of which are overexpressed in Synechocystis. Evidence showed a dual purpose of the nptl gene, as a leader sequence fused to a heterologous geranyl-diphosphate synthase (GPPS), promoting its expression, while at the same time serving as a selectable marker for the screening of transformants. The work further showed that enhanced GPPS expression increased the yield of beta-phellandrene in Synechocystis transformants harboring the beta-PHLS gene. Moreover, the research evaluated the expression efficacy of a DNA fragment comprising 87 nucleotides from the S' end of the cmR gene in fusion with the GPPS gene. This short fusion construct substantially increased the intracellular geranyl-diphosphate synthase level, suggesting that "short-stretch" cmR leader sequences can be used to drive a higher expression level of heterologous biosynthetic genes, while avoiding undesirable internal recombinations, as these sequences are shorter than the threshold of 200 bp, commonly assumed to be the threshold of high efficiency recombinations.

Heterologous Leader Sequences in Fusion Constructs Enhance Expression of Geranyl Diphosphate Synthase and Yield of β-Phellandrene Production in Cyanobacteria ( Synechocystis)

Betterle N;
2018-01-01

Abstract

Fusion constructs as protein overexpression vectors proved to be critical in the heterologous expression of terpene synthases in cyanobacteria. The concept was recently applied to the heterologous overexpression of the beta-phellandrene synthase (beta-PHLS) from plants, fused to the highly expressed endogenous cpcB gene encoding the beta-subunit of phycocyanin. Overexpressed CpcB*PHLS fusion proteins enhanced the heterologous yield of C10H16 beta-phellandrene hydrocarbons production in Synechocystis. This work extended the concept of fusion constructs as protein overexpression vectors by showing that highly expressed heterologous genes could also serve as leader sequences for protein overexpression in cyanobacteria. Examined are the kanamycin nptI and chloramphenicol cmR resistance cassettes, both of which are overexpressed in Synechocystis. Evidence showed a dual purpose of the nptl gene, as a leader sequence fused to a heterologous geranyl-diphosphate synthase (GPPS), promoting its expression, while at the same time serving as a selectable marker for the screening of transformants. The work further showed that enhanced GPPS expression increased the yield of beta-phellandrene in Synechocystis transformants harboring the beta-PHLS gene. Moreover, the research evaluated the expression efficacy of a DNA fragment comprising 87 nucleotides from the S' end of the cmR gene in fusion with the GPPS gene. This short fusion construct substantially increased the intracellular geranyl-diphosphate synthase level, suggesting that "short-stretch" cmR leader sequences can be used to drive a higher expression level of heterologous biosynthetic genes, while avoiding undesirable internal recombinations, as these sequences are shorter than the threshold of 200 bp, commonly assumed to be the threshold of high efficiency recombinations.
2018
cyanobacteria
fusion protein
metabolic engineering
photosynthesis
terpene synthesis
β-phellandrene
Alkyl and Aryl Transferases
Bacterial Proteins
Biomass
Cyclohexane Monoterpenes
Cyclohexenes
DNA, Bacterial
Erythritol
Monoterpenes
Nucleotides
Operon
Photosynthesis
Plasmids
Recombination, Genetic
Substrate Specificity
Synechocystis
Transformation, Genetic
Transgenes
Protein Sorting Signals
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11562/1059552
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