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Table 1 Sequences of primers used for this study

From: Metabolic engineering of Rhodopseudomonas palustris for the obligate reduction of n-butyrate to n-butanol

Primer

Length

Sequence (5′ → 3′)

Purpose

pBBR1MCS-2 vector

 XhoI GFPmut2 F1

60

GGCGGCCTCGAGAGGAGGATCTATTCATGAGTAAAGGAGAAGAACTTTTCACTGGAGTTG

Cloning GFPmut2

 XbaI GFPmut2 R1

51

GCCGCCTCTAGACTATTTGTATAGTTCATCCATGCCATGTGTAATCCCAGC

 

 BamHI RBS AdhE2824 F1

68

GCCGCGGATCCAGGAGGATCTATTCATGAAAGTTACAAATCAAAAAGAACTAAAACAAAAGCTAAATG

Cloning adhE2 824

 SacI 6X His AdhE2824 R1

62

CACCCGGAGCTCTAAGTGGTGATGGTGATGATGAAATGATTTTATATAGATATCCTTAAGTT

 

 SacI AdhE2824 R1

43

CACCCGGAGCTCTAAAATGATTTTATATAGATATCCTTAAGTT

 

 XhoI RBS AdhEBisB18 F1

57

GACGACCTCGAGAGGAGGATCTATTCGTGACCTTATCTACCCCGTCCGACCTCGACA

Cloning adhE BisB18

 XbaI 6X His AdhEBisB18 R1

60

CACCCGTCTAGACTAGTGGTGATGGTGATGATGTTCCGCGGCGTTCGCCGTCGCCACCGA

 

 XbaI AdhEBisB18 R1

52

CAGTCACCCGTCTAGACTATTCCGCGGCGTTCGCCGTCGCCACCGACAATGT

 

pMG105P vector

 XbaI GFPmut2 F1

60

GGCGGCTCTAGAAGGAGGATCTATTCATGAGTAAAGGAGAAGAACTTTTCACTGGAGTTG

Cloning GFPmut2

 SalI GFPmut2 R1

53

GGCGGCCGGTCGACCTATTTGTATAGTTCATCCATGCCATGTGTAATCCCAGC

 
  1. Restriction sites are underlined