Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2020221 | Protein Expression and Purification | 2016 | 6 Pages |
Abstract
Selected model strains of phototrophic cyanobacteria have been genetically engineered for heterologous expression of numerous enzymes. In the present study, we initially explored the heterologous expression of enzymes involved in trans-resveratrol production, namely, the production of tyrosine ammonia-lyase, coumaroyl CoA-ligase, and stilbene synthase, in the unicellular cyanobacterium Synechocystis PCC 6803. Under the promoters Ptrc1Ocore and Ptrc1O, the respective genes were transcribed and translated into the corresponding soluble proteins at concentrations of 16-34 μg Lâ1. The expression levels of these enzymes did not affect the growth rate of the cyanobacterial cells. Interestingly, coumaroyl CoA-ligase expression slightly increased the chlorophyll a content of the cells. Overall, our results suggest that the complete pathway of trans-resveratrol production can be engineered in Synechocystis PCC 6803.
Keywords
PBS containing Tween 20RNAPChl aPBSRT-PCRPBSTPALSTS4CLC4HSynechocystis PCC 6803trans-ResveratrolRNA polymeraseTALCinnamic acid 4-hydroxylaseSDS-PAGESodium dodecyl sulfate polyacrylamide gel electrophoresisHeterologous expressionTyrosine ammonia-lyaseCyanobacteriaStilbene synthasephenylalanine ammonia-lyasePhosphate-buffered salinereverse transcription polymerase chain reactionChlorophyll a
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Authors
Supaluk Tantong, Aran Incharoensakdi, Supaart Sirikantaramas, Peter Lindblad,