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Table 1 Results of dual-phase fermentations of the recombinant strains in sealed bottles after 48 h

From: Metabolic engineering of Escherichia coli for l-malate production anaerobically

Straina

Consumed glucose (g/L)

Fermentation product titer (g/L)

Malate yieldb (g/g)

Pyruvate

Succinate

Malate

BA040

8.50 ± 0.24

0.97 ± 0.02

1.23 ± 0.02

1.73 ± 0.04

0.20 ± 0.01

BA041

10.50 ± 0.42

1.85 ± 0.08

2.46 ± 0.05

3.53 ± 0.25

0.34 ± 0.01

BA042

14.50 ± 0.20

2.52 ± 0.15

1.87 ± 0.08

4.39 ± 0.12

0.30 ± 0.01

BA050

9.50 ± 0.50

1.81 ± 0.21

1.58 ± 0.01

3.22 ± 0.36

0.34 ± 0.01

BA051

11.50 ± 0.50

1.69 ± 0.50

1.46 ± 0.02

5.30 ± 0.50

0.46 ± 0.50

BA052

10.00 ± 0.45

0.58 ± 0.01

1.85 ± 0.05

4.39 ± 0.21

0.44 ± 0.01

BA061

15.00 ± 0.42

2.87 ± 0.22

1.79 ± 0.02

9.39 ± 0.42

0.63 ± 0.01

BA062

15.00 ± 0.55

2.89 ± 0.14

1.45 ± 0.01

9.19 ± 0.55

0.61 ± 0.01

BA063

18.00 ± 0.46

2.67 ± 0.15

1.25 ± 0.02

13.14 ± 0.35

0.73 ± 0.01

  1. Fermentations were carried out in a 100 mL sealed bottle with 30 ml LB medium with 30 g/L glucose and 16 g/L magnesium carbonate hydroxide (37 °C, 170 rpm). Anaerobiosis was achieved during growth with added bicarbonate to ensure an atmosphere of CO2
  2. aAll the strains were tested with a two-stagedual-phase process (aerobic cell growth and anaerobic L-malate production), average fermentation characteristics from triplicate sealed bottle fermentations are shown
  3. b Yield was calculated as grams of L-malate produced per gram of glucose consumed