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. 2017 Mar 13;17(6):695–709. doi: 10.1002/elsc.201600225

Table 1.

Experimental data of Yarrowia lipolytica ACA‐YC 5033 in nitrogen‐limited glucose‐based media with OMWs added in various amounts

Initial phenolic compounds (g/L) Fermentation time (h) X (g/L) L (g/L) Cit (g/L) Glccons (g/L) YX/Glc (g/g) YL/X (g/g) YCit/Glc (g/g)
0.00c Shake‐flasks Aseptic 120 5.5 ± 0.4a ) 0.40 ± 0.05 13.8 ± 1.0 23.7 ± 1.5 0.23 0.07 0.58
24 4.2 ± 0.3a 0.50 ± 0.05 0.0 5.4 ± 0.5 0.78 0.12 0.00
144 5.5 ± 0.3b 0.30 ± 0.05 18.9 ± 1.5 25.8 ± 1.5 0.21 0.05 0.73
2.00 ± 0.20 Shake‐flasks Aseptic 120 4.1 ± 0.3a ) 0.70 ± 0.10 13.5 ± 1.0 23.3 ± 1.5 0.18 0.16 0.58
96 4.0 ± 0.3a 0.80 ± 0.05 12.2 ± 1.0 15.8 ± 1.0 0.25 0.19 0.77
168 3.7 ± 0.3b 0.50 ± 0.05 18.2 ± 1.5 23.7 ± 1.5 0.15 0.15 0.77
2.90 ± 0.25 Shake‐flasks Aseptic 121 3.7 ± 0.3a ) 0.60 ± 0.05 17.2 ± 1.0 22.5 ± 1.5 0.16 0.16 0.76
96 3.6 ± 0.3a 1.00 ± 0.10 15.1 ± 1.0 18.7 ± 1.5 0.20 0.27 0.81
144 3.5 ± 0.3b 0.70 ± 0.05 19.0 ± 1.5 25.6 ± 2.0 0.14 0.20 0.74
Shake‐flasks Pasteurized 120 3.3 ± 0.2a) , a 0.90 ± 0.10 11.6 ± 1.0 17.0 ± 1.0 0.19 0.26 0.68
178 3.2 ± 0.2b 0.60 ± 0.05 15.5 ± 1.0 22.8 ± 1.5 0.14 0.19 0.68
Shake‐flasks Glc0≈80.0 g/L Aseptic 288 4.6 ± 0.3a ) 1.20 ± 0.10 43.3 ± 3.5 70.7 ± 5.0 0.07 0.26 0.61
240 4.3 ± 0.3a 1.40 ± 0.10 38.3 ± 3.5 57.3 ± 4.0 0.08 0.33 0.67
384 4.5 ± 0.3b 0.80 ± 0.10 51.9 ± 4.0 81.6 ± 5.0 0.06 0.18 0.64
Bioreactor Aseptic 188 4.7 ± 0.3a) , b 0.90 ± 0.10 15.2 ± 1.0 25.0 ± 2.0 0.19 0.19 0.61
138 4.3 ± 0.3a 1.10 ± 0.10 13.4 ± 1.0 21.7 ± 1.5 0.20 0.26 0.62
Bioreactor Pasteurized 192 4.8 ± 0.3a) , b 0.80 ± 0.05 13.9 ± 1.0 23.9 ± 1.5 0.20 0.17 0.58
144 4.4 ± 0.3a 1.00 ± 0.10 12.1 ± 1.0 19.7 ± 1.5 0.22 0.22 0.61
4.50 ± 0.35 Shake‐flasks Aseptic 243 2.1 ± 0.1a) , b 0.40 ± 0.05 4.0 ± 0.5 7.4 ± 0.5 0.29 0.18 0.55
48 1.7 ± 0.1a 0.80 ± 0.05 1.0 ± 0.5 4.3 ± 0.5 0.40 0.45 0.24
5.50 ± 0.40 216 3.0 ± 0.3a) , b 0.90 ± 0.10 2.2 ± 0.5 6.1 ± 0.5 0.50 0.30 0.36
48 2.6 ± 0.1a 1.20 ± 0.10 0.4 ± 0.5 3.6 ± 0.5 0.72 0.48 0.11

Representations of total biomass (X, g/L), total cellular lipid (L, g/L), total citric acid (Cit, g/L) and consumed substrate (Glccons, g/L) concentrations at different fermentation points of each trial.

when Xmax concentration was achieved;

a

when Lmax concentration was achieved;

b

when Citmax concentration was achieved;

c

Results regarding control experiment (no OMW addition) were obtained from Sarris et al. 22.

Fermentation time, conversion yield of biomass produced per glucose consumed (YX/Glc, g/g), total lipid in dry biomass (YL/X, g/g) and conversion yield of total citric acid produced per glucose consumed (YCit/Glc, g/g) are presented for all points of the trials. Culture conditions: growth on aseptic and pasteurized 250‐mL flasks at 180 ± 5 rpm, Glc0 = 35.0 ± 2.0 g/L, (NH4)2SO4 = 0.5 g/L, yeast extract = 0.5 g/L, initial pH = 6.0 ± 0.1, pH ranging between 5.0 and 6.0, DOT>20% v/v, incubation temperature T = 28°C; growth on aseptic and pasteurized batch bioreactor, 300 rpm, initial phenolic compounds concentration 2.90 ± 0.25 g/L, initial pH = 6.00 ± 0.02, incubation temperature T = 28°C and sparging of air at 1.0 vvm. Each point is the mean value of two independent measurements.