Skip to main content

Table 1 Mutations that occurred in the evolved PB13 strain during the ALE process

From: Deletion of the 2-acyl-glycerophosphoethanolamine cycle improve glucose metabolism in Escherichia coli strains employed for overproduction of aromatic compounds

Gene

Basic description

Mutations

  

JM101

PB13

Nucleot.

Pos/Chan

(A) JM101 vs PB13 Non-synonymous point mutations (WG)

 

Hypothetical/putative/unknown function genes

    

 wzyE

Predicted Wzy protein involved in ECA polysaccharide chain elongation

GCG

GtG

221

74 A-V

 ydiM

Predicted transporter of the major facilitator superfamily (MFS) of transporters

TTC

cTC

982

328 F-L

 ydaF

Predicted protein

ACT

AaT

116

39 T-N

 

Metabolism and transport

    

 bglA

One of several 6-phospho-β-glucosidases in E. coli

CCG

CtG

839

280 P-L

 deoB

Phosphodeoxyribomutase; catabolic enzyme of the pyrimidine deoxyribonucleosides degradation pathway

GAC

GgC

848

283 D-G

 dhaM

Dihydroxyacetone kinase subunit M, homologous to certain PTS components

TGg

TGa

1038

346 W-stop

 glpT

Major uptake transporter for glycerol-3-phosphate, belongs to the major Facilitator Superfamily (MFS)

CCG

CtG

416

139 P-L

 ispG

IspG, catalyzes the sixth step in the methylerythritol phosphate pathway

GTC

GcC

749

250 V-A

 mepA

Penicillin-insensitive d-alanyl-d-alanine (DD) endopeptidase

CGT

CaT

197

66 R-H

 msbA

ATP-binding lipopolysacchride transport complex

ACG

gCG

367

123 T-A

 xapB

Xanthosine MFS transporter

ACC

gCC

1051

351 T-A

 ydcT

YdcT is an ATP-binding component of a predicted spermidine/putrescine ABC transporter

CCG

CtG

113

38 P-L

 

Cellular constituents

    

 fliN

FliN, is one of three components of the flagellar motor’s “switch complex”

GAT

GgT

371

124 D-G

 

Regulatory genes

    

 polA

DNA Polymerase I (Pol I)

GCG

GtG

2084

695 A-V

(B) JM101 vs PB13 Deletions (WG)

 

 ptsP

Member of a second PTS chain involved in nitrogen metabolism

Pres

Abs

 rppH

RNA pyrophosphohydrolase that initiates mRNA degradation by hydrolysis of the 5′-triphosphate end

Pres

Abs

 ygdT

Hypothetical protein

Pres

Abs

 mutH

dGATC endonuclease in the MutHLS complex, the methyl-directed mismatch repair pathway

Pres

Abs

 ygdQ

Putative transport protein

Pres

Abs

 ygdR

Predicted protein

Pres

Abs

 tas

Putative NAD(P)-linked reductase that acts in starvation-associated mutations

Pres

Abs

 lplT

Lysophospholipid transporter (LplT)

Pres

Abs

 aas

2-acylglycerophosphoethanolamine acyltransferase/acyl-ACP synthetase

Pres

Abs

 omrA

Small RNA that is involved in regulating the protein composition of the outer membrane

Pres

Abs

 omrB

Small RNA that is involved in regulating the protein composition of the outer membrane

Pres

Abs

 galR

DNA-binding transcription factor; represses transcription of the operons involved in transport and catabolism of D-galactose

Pres

Abs

  1. A: presents the 13 non-synonymous point mutations in structural genes that changed the code for a different amino acid when compared to the parental PB11 and JM101 strains genomes. In addition 8 synonymous point mutations in different genes were also detected (Additional file 1: Table S1). The non-synonymous point mutations dhaM and glpT shared by PB12 [4] and PB13 strains are in italic letters. B: presents lost genes in the chromosomal region deleted. Basic descriptions of these genes were taken from http://www.ecocyc.org. WG Winter Genomics Inc.