Use of Immobilized Candida Cells on Xylitol Production from Sugarcane Bagasse
Walter de Carvalho3, Silvio Silvério da Silva3*, Michele Vitolob,
Ismael Maciel de Mancilha 3
a Department of Biotechnology, Faculty of Chemical Engineering of Lorena,
Lorena, SP, 12600-000, Brazil. Fax: (+55) 1 25533165.
E-mail: silvio@debiq.faenquil.br
b Faculty of Pharmaceutical Sciences, University of Säo Paulo, Säo Paulo,
SP, 05489-900, Brazil
* Author for correspondence and reprint requests
Z. Naturforsch. 55c, 213-217 (2000); received September 10/December 6, 1999
Immobilization, Candida guilliermondii , Xylitol, Sugarcane Bagasse
In this study we used the yeast Candida guilliermondii FTI 20037 immobilized by entrap
ment in Ca-alginate beads (2.5-3 mm diameter) for xylitol production from concentrated
sugarcane bagasse hemicellulosic hydrolysate in a repeated batch system. The fermentation
runs were carried out in 125- and 250-ml Erlenmeyer flasks placed in an orbital shaker at
30 °C and 200 rpm during 72 h, keeping constant the proportion between work volume and
flask total volume. According to the results, cell viability was substantially high (98%) in all
fermentative cycles. The values of parameters xylitol yield and volumetric productivity
increased significantly with the reutilization of the immobilized biocatalysts. The highest val
ues of xylitol final concentration (11.05 g/1), yield factor (0.47 gig) and volumetric producti
vity (0.22 g/lh) were obtained in 250-ml Erlenmeyer flasks containing 80 ml of medium plus
20 mi of immobilized biocatalysts. The support used in this study (Ca-alginate) presented
stability in the experimental conditions used. The results show that the use of immobilized
cells is a promising approach for increasing the xylitol production rates.
Introduction
Xylitol is a polyalcohol with a sweetening power
comparable to that of sucrose (Bär, 1986). This
poliol, used in provision industries in the Scandi
navian countries (Hahn-Hägerdal et al ., 1994), has
stood out in the last years for its anticariogenic
properties (Pepper and Olinger, 1988) and for its
clinical applications as a sugar substitute in cases
of diabetes, obesity, deficiency in glucose 6 P dehy
drogenase enzyme and problems in the metabo
lism of lipids (Ylikahri, 1979).
From the discovery of the ability of certain
yeasts to ferment xylose as a source of carbon and
energy (Schneider et al., 1981; Slininger et al.,
1982), the interest of scientists in xylitol pro
duction by biotechnological means has increased
worldwide, since this process has several advan
tages over the conventional chemical process
(Ojamo et al., 1988). In fact, several researchers
have pursuing the development of an economical
and feasible technique for xylitol bioproduction
from lignocellulosic materials.
The bioconversion of xylose into xylitol can be
made by the use of mold, bacteria, yeasts or puri
fied enzymes (Winkelhausen and Kuzmanova,
1998). The yeast Candida guilliermondii FTI
20037, selected in our laboratories (Barbosa et al.,
1988), has proven suitable for this bioprocess,
mainly when lignocellulosic materials like eucalyp
tus chips (Felipe et al., 1996a), rice straw (Roberto
et al., 1996) and sugarcane bagasse (Silva et al.,
1997) are used as sources of xylose.
Lignocellulosic biomass is a potential renewable
source of carbohydrates that can be used as sub
strates in biotechnological processes. Before bio
logical utilization, the biomass needs to be hy
drolysed in order to remove the sugars from the
polymeric fraction. Acid hydrolysis of the hemicel
lulosic fraction produces mainly pentose sugars,
xylose being the major component (Parajö et al.,
1996). Sugarcane bagasse is an appropriate raw
material for xylitol production, since its hemicellu
losic fraction contains 80% of xylose (Kuhad and
Singh, 1993). Besides, from the ecological point of
view, the adoption of technologies employing this
material would prevent serious storage problems
and environmental pollution caused by the sur-
phus of bagasse (Burgi, 1988). On the other hand,
hemicellulosic hydrolysates obtained through acid
hydrolysis contains several inhibitory substances,
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