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Table 1 Strains, plasmids, and primers used in this study

From: Metabolic engineering of Serratia marcescens MG1 for enhanced production of (3R)-acetoin

Strains, plasmids and primers

Description

Source

E.coli S17-1(λ pir)

recA thi pro hsdR M + RP4::2-Tc::Mu::Km Tn7 lysogenized with λ pir phage

Laboratory stock

S. marcescens MG1

Wild type, TcrApr

Laboratory stock

MG12

S. marcescens MG1 ΔslaC

This study

MG13

S. marcescens MG1 ΔgldA

This study

MG14

S. marcescens MG1 ΔslaCΔgldA

This study

MG15

S. marcescens MG1 ΔslagldA/pACPC-slaR

This study

MG16

S. marcescens MG1 ΔslagldA/pACPAB-slaR

This study

MG17

S. marcescens MG1 ΔslagldA/pACPR-slaR

This study

pUTKm1

Apr Kmr oriR6 K oriTRP4

(Lorenzo et al. 1990)

pUT-slaC

pUTKm1 containing a 1798 bp deletion of slaC

This study

pUT-gldA

pUTKm1 containing a 1804 bp deletion of gldA

This study

pACYC184

CmR

(Sun et al. 2015)

pACPC-slaR

pACYC184 containing slaR under the promotor of slaC

This study

pACPA-slaR

pACYC184 containing slaR under the promotor of slaA

This study

pACPR-slaR

pACYC184 containing slaR under the promotor of slaR

This study

slaC-F1

GTggtaccCATGCGGCAAGGAGCGCCATC

This study

slaC-F2

GGCCTGTGCGTTAACGCGAGACCTCCTCCATGTGAAC

This study

slaC-R1

GTTCACATGGAGGAGGTCTCGCGTTAACGCACAGGCC

This study

slaC-R2

GTgagtactCAGCCGCATCAGCCGCTAC

This study

gldA-F1

TTCggtaccGGTTGCGTTCAATGATGATG

This study

gldA-F2

CTCCCTACAAGGATCCGGTTTACCCTTGGGGCGCGGTGTGC

This study

gldA-R1

GCACACCGCGCCCCAAGGGTAAACCGGATCCTTGTAGGGAG

This study

gldA-R2

GCTagatctCTGCATGCTGGTCTGCTTGG

This study

P C-1

GTtctagaTCGCGGCCGCCTGCGGGC

This study

P C-2

GTaagcttGAGACCTCCTCCATGTG

This study

P A-1

GCtctagaAAAACGTAATATACGTTT

This study

P A-1

GCaagcttCTGACTGAGGAGGTGGTC

This study

P R-1

GCtctagaCTGACTGAGGAGGTGGTCGC

This study

P R-2

GCaagcttTTTTGCATTATATGCAAA

This study

slaR-1

GCaagcttATGAATGACGCACGCTATG

This study

slaR-2

GCggatccAATAGGGGTCGACCCGCCAA

This study