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al., 1990; Irnpooisup et ai., 1989a) and <strong>bioreactor</strong> operation modes (Hardjito et al., 1993;<br />

Ogden and Davis, 1991; Ryti and Lee, 1988). Cumntly no effective methods an<br />

available for cornerciai scale culture <strong>of</strong> recombinant ceh in the absence <strong>of</strong> selection<br />

pressure (Kumar and Schuged. 1990). Investigations <strong>of</strong> the possible merits <strong>of</strong><br />

immobilization for these recombinant cclls are tutder way. Numemus benefits with<br />

immobilization have been fowid. Ceii irnmobilization provides a promising alternative for<br />

successful commercial exploitation <strong>of</strong> the enpineered organisms.<br />

1.3. Investigations <strong>of</strong> Imrnobillzed Recombinant Yeast Systeas<br />

irnmobilization <strong>of</strong> enzymes and cells <strong>by</strong> various methods has been widely used to inaease<br />

biological productivity in <strong>bioreactor</strong>s ( Moo-Young, 1988; Overgaard et 1, 1989).<br />

Immobiüzed ceils have r number <strong>of</strong> advantages over k cek High cellular<br />

concentration leading to enhanced metabolic activitits and productivity. separation <strong>of</strong> ceb<br />

hm media facilitaring downsaeam treatment, suitability for repeated use for longer<br />

periods enhancing process efficiency, and a stabilizing effect prolonging biocatalytic<br />

activity are advantages <strong>of</strong> Ynrnobüized systems. Becatue <strong>of</strong> these advantages, a number <strong>of</strong><br />

reports about imrnobilized recombinant cellî have appeared in the liteninire. Enhanced<br />

genetic stability, high cell concentration and expression <strong>of</strong> recombinant <strong>protein</strong>s have been<br />

demonsaated in various recombinant cell systuns in the absence <strong>of</strong> sekction pressun<br />

( Kumar and Schugerl, 1990 ). These reports are stunmarized in Table 13.

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