Cells of Saccharomyces cerevisiae (ATCC 24858) were encapsulated in th
e calcium alginate membrane and cultured. Swelling of the capsule was
prevented by adding 0.2 g CaCl2 to 1 L growth medium. The dry cell con
centration based on the inner volume of the capsule reached 309 g/L, w
hich was much higher than could be obtained by cell entrapment. Ah the
cells remained inside the capsule during the cultivation. The flux of
CO2 through the capsule membrane increased approximately twice by add
ing a nonionic surfactant to the CaCl2 solution during the step of cap
sule formation.