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Table 1 Plasmids and strains used in this study

From: Artificial de novo biosynthesis of hydroxystyrene derivatives in a tyrosine overproducing Escherichia coli strain

Plasmid or strain

Relevant characteristics

Source

Plasmid

 pET-22b(+)

f1 ori, T7 promoter, AmpR

Novagen

 pET-28a(+)

f1 ori, T7 promoter, KanR

Novagen

 pET-opTAL

pET-28a(+) carrying codon-optimized tyrosine ammonia lyase gene (tal)

Kang et al. [20]

 pET-Sam5

pET-28a(+) carrying 4-coumarate 3-hydroxylase gene (sam5)

Choi et al. [17]

 pET-COM

pET-28a(+) carrying caffeic acid methyltransferase gene (com)

Choi et al. [17]

 pET-opT5

pET-28a(+) carrying tal and sam5 gene

Kang et al. [20]

 pET-opT5M

pET-28a(+) carrying tal, sam5, and com gene

Kang et al. [20]

 pET28-tyrA*

pET-28a(+) carrying feedback-inhibition resistant chorismate mutase/prephenate dehydrogenase gene (tyrAfbr)

Kang et al. [20]

 pET22-aroG*

pET-22b(+) carrying feedback-inhibition resistant DAHP synthase gene (aroGfbr)

Kang et al. [20]

 pET-AG

pET-28a(+) carrying tyrAfbr and aroGfbr gene

This study

 pET22-baPAD

pET-22b(+) carrying codon-optimized phenolic acid decarboxylase gene (pad)

This study

 pET-opTD

pET-28a(+) carrying tal and pad gene

This study

 pET-opT5D

pET-28a(+) carrying tal, sam5 and pad gene

This study

 pET-opT5MD

pET-28a(+) carrying tal, sam5, com and pad gene

This study

Strain

 E. coli DH5α

Cloning host

Invitrogen

 E. coli C41(DE3)

Derivative strain of E. coli BL21(DE3)

Miroux and Walker [31]

 ΔtyrR

tryR gene in-frame deletion mutant of E. coli C41(DE3)

Kang et al. [20]

 ΔCOS1

E. coli C41(DE3); ΔtyrR::tyrA fbr, aroG fbr; tyrosine overproducing strain

This study