TABLE 4.
Strain | Mediumb | ΔOD620 | μmax (OD620 unit h−1)c | Glucose consumption (mmol/liter) | Lactic acid production (mmol/liter) | Acetic acid production (μmol/liter) | Ethanol production (mmol/liter) | Electron balance (%)d | Carbon balance (%)e | NAD+/NADH ratio | Theoretical ATP/glucose yield |
---|---|---|---|---|---|---|---|---|---|---|---|
W. cibaria P9 | Control | 0.244 ± 0.020C | 0.027 ± 0.006CD | 25 ± 2C | 25 ± 1A | 921 ± 205F | 30 ± 2A | 111 ± 8AB | 105 ± 8A | 37 ± 2E | 1.03 ± 0.04F |
Caffeic acid | 0.279 ± 0.022C | 0.036 ± 0.003BC | 25 ± 1C | 26 ± 2A | 1,948 ± 225C | 24 ± 1C | 94 ± 7BCD | 102 ± 3A | 38 ± 3E | 1.15 ± 0.03DE | |
p-Coumaric acid | 0.315 ± 0.018AB | 0.049 ± 0.004A | 24 ± 2C | 23 ± 3A | 1,908 ± 106C | 22 ± 2C | 91 ± 3D | 95 ± 13A | 46 ± 3C | 1.06 ± 0.07EF | |
Ferulic acid | 0.259 ± 0.022C | 0.031 ± 0.006BCD | 25 ± 3C | 25 ± 2A | 1,122 ± 261EF | 25 ± 2B | 98 ± 5BCD | 101 ± 12A | 30 ± 5E | 1.05 ± 0.09EF | |
W. cibaria/W. confusa POM12 | Control | 0.281 ± 0.023C | 0.030 ± 0.005BCD | 25 ± 3C | 27 ± 1A | 1,522 ± 207DE | 29 ± 2AB | 112 ± 7AB | 108 ± 13A | 15 ± 10F | 1.13 ± 0.04DE |
Caffeic acid | 0.302 ± 0.021ABC | 0.039 ± 0.005B | 23 ± 1C | 25 ± 2A | 2,369 ± 234B | 23 ± 2C | 96 ± 4CD | 105 ± 10A | 36 ± 3E | 1.20 ± 0.04CD | |
p-Coumaric acid | 0.271 ± 0.016C | 0.031 ± 0.002CD | 20 ± 1B | 22 ± 1B | 2,189 ± 123BC | 22 ± 1C | 101 ± 3AB | 108 ± 9A | 39 ± 3DE | 1.22 ± 0.03C | |
Ferulic acid | 0.286 ± 0.022ABC | 0.029 ± 0.003D | 25 ± 2C | 28 ± 1A | 2,194 ± 132BC | 23 ± 2C | 85 ± 8D | 104 ± 11A | 45 ± 4CD | 1.21 ± 0.04CD | |
L. curvatus PE5 | Control | 0.333 ± 0.020A | 0.028 ± 0.003D | 20 ± 3BC | 22 ± 2AB | 2,385 ± 234B | 28 ± 2AB | 124 ± 18A | 115 ± 16A | 48 ± 4C | 1.21 ± 0.08BCD |
Caffeic acid | 0.337 ± 0.021A | 0.030 ± 0.004BCD | 17 ± 2B | 20 ± 3AB | 3,136 ± 263A | 24 ± 1C | 121 ± 25ABC | 118 ± 19A | 50 ± 4C | 1.37 ± 0.08B | |
p-Coumaric acid | 0.346 ± 0.019A | 0.033 ± 0.002BCD | 12 ± 1A | 18 ± 2C | 3,332 ± 201A | 21 ± 3C | 141 ± 37A | 132 ± 31A | 74 ± 5B | 1.83 ± 0.12A | |
Ferulic acid | 0.331 ± 0.025A | 0.032 ± 0.002BCD | 18 ± 3B | 20 ± 2B | 2,585 ± 261B | 23 ± 2C | 104 ± 19ABCD | 111 ± 18A | 65 ± 4B | 1.27 ± 0.07BC | |
L. rossiae 2MR8 | Control | 0.154 ± 0.031D | 0.012 ± 0.002E | 10 ± 2A | 12 ± 1D | 1,277 ± 237DEF | 13 ± 1D | 124 ± 21AB | 118 ± 19A | 13 ± 2F | 1.32 ± 0.08BC |
Ferulic acid | 0.251 ± 0.026C | 0.032 ± 0.002BCD | 13 ± 1A | 14 ± 2D | 2,050 ± 224BC | 12 ± 2D | 83 ± 17CD | 106 ± 8A | 175 ± 9A | 1.24 ± 0.09BCD |
Values were obtained after fermentation for 24 h at 30°C with lactic acid bacterial strains. Means within the column with different superscript letters are significantly different (P < 0.05). ΔOD620, increase in cell density; μmax, maximum growth rate.
CDM was prepared as described by McFeeters and Chen (20) and supplemented with caffeic, p-coumaric, or ferulic acid at a concentration of 2 mM. CDM not supplemented with hydroxycinnamic acids was used as a control. The data are the means of three independent experiments ± standard deviations (n = 3).
Growth data were modeled according to the Gompertz equation, as modified by Zwietering et al. (21).
Electron balances were calculated by considering the stoichiometry of the electron donors and electron acceptors involved in glucose metabolism.
Carbon balances were calculated by assuming the production of 1 mmol CO2 per mmol glucose.