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Table 2 Fractional abundance of unlabeled amino acid fragments (m0) during cultivation on labeled glucose with and without unlabeled proline

From: Metabolic network capacity of Escherichia coli for Krebs cycle-dependent proline hydroxylation

 

wt_pET

ΔputA_pET

wt_p4h1of

ΔputA_p4h1of

−Pro

+Pro

−Pro

+Pro

−Pro

+Pro

−Pro

+Pro

Glycolysis

 Ala [M-57]+

0.366

0.377

0.366

0.368

0.365

0.360

0.361

0.359

 Gly [M-57]+

0.622

0.624

0.621

0.622

0.621

0.621

0.619

0.620

 Val [M-57]+

0.175

0.183

0.176

0.175

0.174

0.169

0.169

0.165

 Leu [M-159]+

0.113

0.12

0.114

0.114

0.113

0.105

0.109

0.104

 Ser [M-57]+

0.319

0.322

0.321

0.321

0.313

0.311

0.313

0.310

 Phe [M-57]+

0.111

0.114

0.111

0.110

0.113

0.109

0.109

0.108

TCA

 Asp [M-57]+

0.195

0.336

0.194

0.194

0.191

0.233

0.187

0.179

 Thr [M-57]+

0.193

0.331

0.190

0.190

0.187

0.232

0.184

0.176

 Ile [M-159]+

0.140

0.225

0.140

0.140

0.137

0.157

0.135

0.128

 Glu [M-57]+

0.115

0.333

0.115

0.115

0.113

0.195

0.112

0.105

 Pro [M-159]+

0.184

0.818

0.181

0.819

0.176

0.819

0.175

0.820

  1. Cells were grown aerobically at 30°C in M9 medium with 5 g L−1 labeled glucose (80% 1-13C and 20% U-13C) in the presence (+Pro) and absence (−Pro) of 5 mM unlabeled proline. wt_pET, E. coli BL21(DE3)(pLysS)(pET-24a); ΔputA_pET, E. coli BL21ΔputA(DE3)(pLysS)(pET-24a); wt_p4h1of, E. coli BL21(DE3)(pLysS)(pET_p4h1of); ΔputA_p4h1of, E. coli BL21ΔputA(DE3)(pLysS)(pET_p4h1of).