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1.
J Food Sci ; 80(10): E2217-27, 2015 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-26352877

RESUMEN

In this study, comprehensive characterization and drying methods on properties of bacterial cellulose were analyzed. Bacterial cellulose was prepared by Gluconacetobacter hansenii CGMCC 3917, which was mutated by high hydrostatic pressure (HHP) treatment. Bacterial cellulose is mainly comprised of cellulose Iα with high crystallinity and purity. High-water holding and absorption capacity were examined by reticulated structure. Thermogravimetric analysis showed high thermal stability. High tensile strength and Young's modulus indicated its mechanical properties. The rheological analysis showed that bacterial cellulose had good consistency and viscosity. These results indicated that bacterial cellulose is a potential food additive and also could be used for a food packaging material. The high textural stability during freeze-thaw cycles makes bacterial cellulose an effective additive for frozen food products. In addition, the properties of bacterial cellulose can be affected by drying methods. Our results suggest that the bacterial cellulose produced from HHP-mutant strain has an effective characterization, which can be used for a wide range of applications in food industry.


Asunto(s)
Celulosa/química , Gluconacetobacter/química , Adsorción , Aditivos Alimentarios , Embalaje de Alimentos , Presión Hidrostática , Reología , Resistencia a la Tracción , Viscosidad , Agua/fisiología
2.
Bioresour Technol ; 151: 113-9, 2014 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-24212131

RESUMEN

In order to improve the use of waste beer yeast (WBY) for bacterial cellulose production by Gluconacetobacter hansenii CGMCC 3917, a two-step pre-treatment was designed. First WBY was treated by 4 methods: 0.1M NaOH treatment, high speed homogenizer, ultrasonication and microwave treatment followed by hydrolysis (121°C, 20 min) under mild acid condition (pH 2). The optimal pre-treatment conditions were evaluated by the reducing sugar yield after hydrolysis. 15% WBY treated by ultrasonication for 40 min had the highest reducing sugar yield (29.19%), followed by NaOH treatment (28.98%), high speed homogenizer (13.33%) and microwaves (13.01%). Treated WBY hydrolysates were directly supplied as only nutrient source for BC production. A sugar concentration of 3% WBY hydrolysates treated by ultrasonication gave the highest BC yield (7.02 g/L), almost 6 times as that from untreated WBY (1.21 g/L). Furthermore, the properties of the BC were as good as those obtained from the conventional chemical media.


Asunto(s)
Cerveza/microbiología , Celulosa/biosíntesis , Gluconacetobacter/metabolismo , Saccharomyces cerevisiae/metabolismo , Absorción , Celulosa/ultraestructura , Hidrólisis , Agua/química
3.
Appl Biochem Biotechnol ; 165(7-8): 1519-31, 2011 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-21947710

RESUMEN

Strain M(438), deposited as CGMCC3917 and isolated from inoculums of bacterial cellulose (BC) producing strain screened in homemade vinegar and then induced by high hydrostatic pressure treatment (HHP), has strong ability to produce BC more than three times as that of its initial strain. It is the highest yield BC-producing strain ever reported. In this paper, M(438) was identidied as Gluconacetobacter hansenii subsp. nov. on the basis of the results obtained by examining it phylogenetically, phenotypically, and physiologically-biochemically. Furthermore, the genetic diversity of strain M(438) and its initial strain was examined by amplified fragment length polymorphism. The results indicated that strain M(438) was a deletion mutant induced by HHP, and the only deleted sequence showed 99% identity with 24,917-24,723 bp in the genome sequence of Ga. hansenii ATCC23769, and the complement gene sequence was at 24,699-25,019 bp with local tag GXY_15142, which codes small multidrug resistance (SMR) protein. It can be inferred that SMR might be related to inhibiting BC production to a certain extent.


Asunto(s)
Celulosa/biosíntesis , Gluconacetobacter/química , Gluconacetobacter/metabolismo , Secuencia de Aminoácidos , Análisis del Polimorfismo de Longitud de Fragmentos Amplificados , Proteínas Bacterianas/química , Proteínas Bacterianas/genética , Proteínas Bacterianas/metabolismo , Gluconacetobacter/clasificación , Gluconacetobacter/genética , Presión Hidrostática , Datos de Secuencia Molecular , Filogenia , Alineación de Secuencia
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