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Biofuels in Perspective

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(a)<br />

Cultivation Separation Purification Immobilization Methanolysis<br />

(b)<br />

Cultivation<br />

&<br />

Immobilization<br />

with BSPs<br />

extraction<br />

adsorption<br />

chromatography<br />

crystallization<br />

cross-l<strong>in</strong>k<strong>in</strong>g<br />

covalent bond<strong>in</strong>g<br />

entrapment<br />

Separation Methanolysis<br />

Figure 8.5 Comparison of lipase production processes for methanolysis us<strong>in</strong>g (a) extracellular and (b)<br />

<strong>in</strong>tracellular lipases. (From Ref. 19, with permission of The Society for Biotechnology, Japan.)<br />

(b)<br />

1 mm<br />

(a)<br />

Figure 8.6 Micrographs show<strong>in</strong>g (a) empty, (b) surface and (c) cross-section of 6-mm cubic biomass<br />

support particle (voidage >97 %; pore size: 50 pores per l<strong>in</strong>ear <strong>in</strong>ch). Medium: polypeptone 70 g/l; NaNO3<br />

1.0 g/l; KH2PO4 1.0 g/l; MgSO4 · 7H2O 0.5 g/l; olive oil 30g/l. Culture conditions: medium volume, 100<br />

ml; temperature, 35 ◦ C; cultivation time, 80–90 h; shak<strong>in</strong>g, 150 oscillations/m<strong>in</strong>.<br />

(c)

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