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Table 2 SSF experiments performed with 20% DW pretreated bagasse using the enzyme cocktail GC220 at different enzyme dosages to monomerize sugars, and B. coagulans DSM2314 for fermentation to lactic acid

From: Production of l(+)-lactic acid from acid pretreated sugarcane bagasse using Bacillus coagulans DSM2314 in a simultaneous saccharification and fermentation strategy

SSF

Biomass liquefied with

Enzyme added  %V/DW

Preculture

C La (g/l)

A La (g)

Qv,av (g/l/h)

Q v,max (g/l/h)

Y s/La (%)

Y Lc/La  %

Time (h)a

Batch

Liquid fraction

12.5

Reference

64.1

77.6

0.78

4.2

80

74

90

Batch

Liquid fraction

12.5

Furfural

74.6

91.7

0.92

4.2

94

87

90

Batch

Water

7.5–>10

Furfural

70.6

84.2

0.92

4.4

92

83

84

Batch

Water

15

Furfural

70.4

83.8

1.14

4.2

90

83

68

Two-stage 9.5 h

Water

15

Furfural

58.2

75.9

1.81

4.3

90

73

37

  1. Either liquid fraction acquired after acid pretreatment or MilliQ water is used to solubilize the solids. As inoculum, either a preculture to which furfural was added was used, or a reference preculture was used which did not contain furfural. Addition of 20% DW bagasse fibres was either done as batch at the start of fermentation, or in two stages of 10% DW. Lactic acid was determined via HPLC
  2. C LA concentration of lactic acid at the end of the SSF in g/l
  3. A La total lactic acid produced in g
  4. Q v,av average volumetric lactic acid productivity in g/l/h
  5. Q v,max maximum volumetric lactic acid productivity in g/l/h
  6. Y s/La estimated conversion efficiency of sugar monomers to lactic acid in W/W
  7. Y Lc/La lactic acid production yield on total lignocellulosic sugars in W/W
  8. aTotal fermentation time, from inoculation of SSF to reaching final lactic acid concentration