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1.
Braz. j. microbiol ; 48(1): 180-185, Jan.-Mar. 2017. tab, graf
Article in English | LILACS | ID: biblio-839351

ABSTRACT

Abstract Pullulan is a natural exopolysaccharide with many useful characteristics. However, pullulan is more costly than other exopolysaccharides, which limits its effective application. The purpose of this study was to adopt a novel mixed-sugar strategy for maximizing pullulan production, mainly using potato starch hydrolysate as a low-cost substrate for liquid-state fermentation by Aureobasidium pullulans. Based on fermentation kinetics evaluation of pullulan production by A. pullulans 201253, the pullulan production rate of A. pullulans with mixtures of potato starch hydrolysate and sucrose (potato starch hydrolysate:sucrose = 80:20) was 0.212 h−1, which was significantly higher than those of potato starch hydrolysate alone (0.146 h−1) and mixtures of potato starch hydrolysate, glucose, and fructose (potato starch hydrolysate:glucose:fructose = 80:10:10, 0.166 h−1) with 100 g L−1 total carbon source. The results suggest that mixtures of potato starch hydrolysate and sucrose could promote pullulan synthesis and possibly that a small amount of sucrose stimulated the enzyme responsible for pullulan synthesis and promoted effective potato starch hydrolysate conversion effectively. Thus, mixed sugars in potato starch hydrolysate and sucrose fermentation might be a promising alternative for the economical production of pullulan.


Subject(s)
Ascomycota/metabolism , Starch/metabolism , Sucrose/metabolism , Solanum tuberosum/chemistry , Fermentation , Glucans/biosynthesis , Starch/chemistry , Carbon/metabolism , Kinetics , Biomass , Bioreactors , Batch Cell Culture Techniques
2.
Indian J Biochem Biophys ; 2011 June; 48(3): 170-174
Article in English | IMSEAR | ID: sea-135316

ABSTRACT

A 1312 bp 5' flanking region of Salicornia europaea choline monooxygenase (SeCMO) gene was isolated using the anchored PCR. To investigate the mechanism of regulation for this stress-induced gene, the SeCMO promoter--glucuronidase (GUS) chimeric gene constructs containing five deletions F1, F2, F3, F4 and F5 were introduced into tobacco (Nicotiana tabacum L.) by Agrobacterium-mediated transformation. The functional properties of each promoter fragment were examined by assaying GUS activity in the leaves of transgenic tobacco treated with abiotic stresses (NaCl, PEG6000 and low temperature). The GUS activity in transgenic tobacco with F2 (-1056 to +8) construct showed highest increase under all the three abiotic stresses. Thus, the study provided a potential promoter induced by the salt, dehydration and cold for the plant genetic manipulation.


Subject(s)
Base Sequence , Chenopodiaceae/genetics , Chenopodiaceae/metabolism , Cold Temperature , Glucuronidase/biosynthesis , Glucuronidase/genetics , Molecular Sequence Data , Oxygenases/genetics , Plant Proteins/genetics , Plant Proteins/metabolism , Plants, Genetically Modified/enzymology , Plants, Genetically Modified/genetics , Polyethylene Glycols , Promoter Regions, Genetic/genetics , Sodium Chloride , Tobacco/enzymology , Tobacco/genetics
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