Palatinose production by free and Ca-alginate gel immobilized cells of Erwinia sp.

2007 ◽  
Vol 36 (3) ◽  
pp. 202-208 ◽  
Author(s):  
Haroldo Yukio Kawaguti ◽  
Hélia Harumi Sato
2011 ◽  
Vol 233-235 ◽  
pp. 1171-1176
Author(s):  
Ming Fang Luo ◽  
Hui Zhou Liu

Gram-negative bacterium, Pseudomonas delafieldii R-8 (CGMCC 0570) is capable of desulfurizing dibenzothiophene (DBT) and 4,6-dimethyldibenzothiophene (4,6-DMDBT) to produce corresponding monohydroxydimethylbiphenyl. The immobilization of the resting cells of this strain in Ca-alginate gel effectively improved the stability of the cells and the desulfurization ability per amount of cells. 1 mmol/L of DBT and 4,6-DMDBT could be completely degraded in about 1 d. About 39 percent of the activity for 4,6-DMDBT was recovered after immobilization. The desulfurization activity was increased with the decrease of the diameter of the beads. The Ca-alginate immobilized cells could be used repeatedly for over 190 h with the addition of calcium ions to strengthen them. A thin layer of hydrophobic polyurea was coated on the surface of Ca-alginate gel using a simple method. The desulfurization activity was enhanced after the coating.


2000 ◽  
Vol 55 (3-4) ◽  
pp. 213-217 ◽  
Author(s):  
Walter de Carvalho ◽  
Silvio Silvério da Silva ◽  
Michele Vitolo ◽  
Ismael Maciel de Mancilha

Abstract In this study we used the yeast Candida guilliermondii FTI 20037 immobilized by entrapment 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 values of xylitol final concentration (11.05 g/1), yield factor (0.47 gig) and volumetric productivity (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.


1987 ◽  
Vol 42 (4) ◽  
pp. 408-413 ◽  
Author(s):  
H. Eikmeier ◽  
H. J. Rehm

Abstract The citric acid excretion of Ca-alginate-immobilized cells of Aspergillus niger in batch culture decreased with a half-time of approximately 19 days. Reactivation of the biocatalysts by regeneration in growth medium was possible, but it was followed by a submerged sporulation of the fungus, and medium was highly contaminated with free cells. Citric acid production could better be prolonged by semicontinuous cultivation with medium exchange every 7 or 14 days, respectively. After 32 days the remaining activity in semicontinuous culture was 1.4-fold higher than in comparable batch experiments. Similar improvements were obtained with a continuous process at a dilution rate of 0.125 v/v · d, whereby medium efflux completely free of detaching mycelia.


1981 ◽  
Vol 3 (11) ◽  
pp. 613-618 ◽  
Author(s):  
Argyrios Margaritis ◽  
Pramod K. Bajpai ◽  
J. Blair Wallace

Author(s):  
Prachi Patil ◽  
Rajesh Sharma ◽  
Tushar Banerjee ◽  
Shridhar Patil

Objective: Permeability of hydrophobic steroid substrates across cell membrane is a critical factor during microbial bioconversion. To increase substrate intake, the feasibility of some organic solvents and emulsifiers as substrate carrier on the bioconversion of 6-methylene androstenedione to exemestane was assessed.Methods: Androstenedione, a commonly available steroid precursor, was chemically converted 6-methylene androstenedione. The time course of exemestane accumulation was estimated after addition of 6-methylene androstenedione dissolved in some organic solvents or dispersed with emulsifiers by growing and immobilized cells of Arthrobacter simplex NCIM 2449 in shake flask cultures.  Results: The use of substrate carriers for addition of 6-methylene androstenedione enhanced the bioconversion several folds. With growing bacterium in triplicate flasks, a peak mol % bioconversion recorded was- ethanol (67.25, 72 h); soybean oil + tween 80 (50.37, 48 h); acetone (38.84, 48 h); soybean oil (38.36, 48 h); lecithin (32.73, 48 h), methanol (32.71, 48 h) and tween 80 (10.37, 48 h). As compared to the growing cells, the bioconversion with Ca-alginate immobilized cells was delayed and peak mol % bioconversion was recorded as ethanol (60.78, 120 h); soybean oil + tween 80 (42.98, 120 h);  methanol (40.50,  72 h);  soybean oil (38.36, 48 h);  acetone (31.18, 72h ) and lecithin (33.67, 120 h); tween 80 (13.87, 120 h).Conclusion: The use of substrate carriers for addition of 6-methylene androstenedione increased the permeability of substrate and may be used to increase the yield of exemestane and reduce incubation time.


Chemosphere ◽  
2009 ◽  
Vol 75 (1) ◽  
pp. 121-128 ◽  
Author(s):  
Charlène Chorao ◽  
Franck Charmantray ◽  
Pascale Besse-Hoggan ◽  
Martine Sancelme ◽  
Angela Cincilei ◽  
...  

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