Table 2 PHB production under a two-stage (photoheterotrophy, then heterotrophy) culture.

From: Two-stage (photoautotrophy and heterotrophy) cultivation enables efficient production of bioplastic poly-3-hydroxybutyrate in auto-sedimenting cyanobacterium

Nutrient condition

Acetate supply % (w/v)

PHB content (% w/w DW)

PHB production (mg/L)

% w/w [PHB product/ACT supply]a

NORMAL

0.00

0.1 ± 0.0

1 ± 1

na

0.05

0.1 ± 0.0

2 ± 1

0.0 ± 0.0

0.10

0.6 ± 0.4

9 ± 5

0.7 ± 0.5

0.20

1.5 ± 0.9

22 ± 13

0.1 ± 0.6

0.40

1.8 ± 0.8

28 ± 15

0.7 ± 0.3

-N

0.00

1.4 ± 0.8*

19 ± 10*

na

0.05

0.4 ± 0.2*

6 ± 5

0.8 ± 0.9

0.10

2.2 ± 0.9*

30 ± 11*

2.8 ± 1.0*

0.20

8.6 ± 1.9*

121 ± 23*

6.0 ± 1.1*

0.40

19.5 ± 2.0*

267 ± 16*

6.6 ± 0.4*

-P

0.00

1.3 ± 0.1*

18 ± 4*

na

0.05

1.8 ± 1.0*

25 ± 17*

4.6 ± 3.3*

0.10

7.5 ± 1.5*

97 ± 11*

9.5 ± 1.1*

0.20

14.3 ± 2.5*

203 ± 30*

10.0 ± 1.5*

0.40

36.0 ± 2.8*

531 ± 75*

13.2 ± 1.8*

-N-P

0.00

4.9 ± 1.6*

65 ± 24*

na

0.05

8.3 ± 1.9*

108 ± 30*

21.2 ± 6.0*

0.10

21.4 ± 2.4*

295 ± 37*

29.3 ± 3.7*

0.20

30.7 ± 2.8*

431 ± 45*

21.5 ± 2.2*

0.40

28.5 ± 1.9*

395 ± 9*

9.8 ± 0.2*

  1. Cells were pre-grown under normal photoautotrophy for 16 d and transferred to the specified heterotrophic conditions using the 6-d time culture period yielding the highest PHB contents (Fig. 3). Data are the average ± 1 SD from three to five independent cultures. Asterisks indicate significantly higher levels (P < 0.01, two-tailed t-test) than those obtained from NORMAL nutrient condition and the same acetate supply. na, not applicable. a = [(PHB production, mg/L)]/(ACT supply in the culture medium, mg/L)] × 100, where PHB production is the difference in production at a second-stage heterotrophic culture and at the end of the first-stage photoautotrophic culture.
    Figure 3
    figure 3

    Conversion efficiency (CE) of acetate to PHB in the two-stage cultures of C. fritschii.

    Sixteen-d photoautotrophy-grown cells were transferred to the heterotrophic -N-P medium in the dark up to 10 d with an initial acetate (ACT) concentration of 0.05% or 0.1% (w/v). The residual available ACT level in the culture medium and CE of acetate to PHB was determined at the indicated time points. Data are the average ± 1 SD from six independent cultures.