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Cellulose production and cellulose synthase gene detection in acetic acid bacteria

The ability of acetic acid bacteria (AAB) to produce cellulose has gained much industrial interest due to the physical and chemical characteristics of bacterial cellulose. The production of cellulose occurs in the presence of oxygen and in a glucose-containing medium, but it can also occur during vi...

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Published in:Applied microbiology and biotechnology 2015-02, Vol.99 (3), p.1349-1361
Main Authors: Valera, Maria José, Torija, Maria Jesús, Mas, Albert, Mateo, Estibaliz
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description The ability of acetic acid bacteria (AAB) to produce cellulose has gained much industrial interest due to the physical and chemical characteristics of bacterial cellulose. The production of cellulose occurs in the presence of oxygen and in a glucose-containing medium, but it can also occur during vinegar elaboration by the traditional method. The vinegar biofilm produced by AAB on the air-liquid interface is primarily composed of cellulose and maintains the cells in close contact with oxygen. In this study, we screened for the ability of AAB to produce cellulose using different carbon sources in the presence or absence of ethanol. The presence of cellulose in biofilms was confirmed using the fluorochrome Calcofluor by microscopy. Moreover, the process of biofilm formation was monitored under epifluorescence microscopy using the Live/Dead BacLight Kit. A total of 77 AAB strains belonging to 35 species of Acetobacter, Komagataeibacter, Gluconacetobacter, and Gluconobacter were analysed, and 30 strains were able to produce a cellulose biofilm in at least one condition. This cellulose production was correlated with the PCR amplification of the bcsA gene that encodes cellulose synthase. A total of eight degenerated primers were designed, resulting in one primer pair that was able to detect the presence of this gene in 27 AAB strains, 26 of which formed cellulose.
doi_str_mv 10.1007/s00253-014-6198-1
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The production of cellulose occurs in the presence of oxygen and in a glucose-containing medium, but it can also occur during vinegar elaboration by the traditional method. The vinegar biofilm produced by AAB on the air-liquid interface is primarily composed of cellulose and maintains the cells in close contact with oxygen. In this study, we screened for the ability of AAB to produce cellulose using different carbon sources in the presence or absence of ethanol. The presence of cellulose in biofilms was confirmed using the fluorochrome Calcofluor by microscopy. Moreover, the process of biofilm formation was monitored under epifluorescence microscopy using the Live/Dead BacLight Kit. A total of 77 AAB strains belonging to 35 species of Acetobacter, Komagataeibacter, Gluconacetobacter, and Gluconobacter were analysed, and 30 strains were able to produce a cellulose biofilm in at least one condition. 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The production of cellulose occurs in the presence of oxygen and in a glucose-containing medium, but it can also occur during vinegar elaboration by the traditional method. The vinegar biofilm produced by AAB on the air-liquid interface is primarily composed of cellulose and maintains the cells in close contact with oxygen. In this study, we screened for the ability of AAB to produce cellulose using different carbon sources in the presence or absence of ethanol. The presence of cellulose in biofilms was confirmed using the fluorochrome Calcofluor by microscopy. Moreover, the process of biofilm formation was monitored under epifluorescence microscopy using the Live/Dead BacLight Kit. A total of 77 AAB strains belonging to 35 species of Acetobacter, Komagataeibacter, Gluconacetobacter, and Gluconobacter were analysed, and 30 strains were able to produce a cellulose biofilm in at least one condition. 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This cellulose production was correlated with the PCR amplification of the bcsA gene that encodes cellulose synthase. A total of eight degenerated primers were designed, resulting in one primer pair that was able to detect the presence of this gene in 27 AAB strains, 26 of which formed cellulose.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>25381910</pmid><doi>10.1007/s00253-014-6198-1</doi><tpages>13</tpages></addata></record>
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subjects Acetic acid
Acetic Acid - metabolism
acetic acid bacteria
Acetobacter
Amino Acid Sequence
Applied Genetics and Molecular Biotechnology
Bacteria
Bacteria - enzymology
Bacteria - genetics
Bacteria - isolation & purification
Bacteria - metabolism
Bacterial Proteins - chemistry
Bacterial Proteins - genetics
Bacterial Proteins - metabolism
biofilm
Biofilms
Biomedical and Life Sciences
Biosynthesis
Biotechnology
Blueberry Plants - microbiology
Carbon
Carbon sources
Cellulose
Cellulose - biosynthesis
cellulose synthase
Ethanol
fluorescence microscopy
Gene expression
Genes
Genetic aspects
Gluconacetobacter
Gluconobacter
Glucose
Glucosyltransferases - chemistry
Glucosyltransferases - genetics
Glucosyltransferases - metabolism
Identification and classification
ISO standards
Laboratories
Life Sciences
Microbial Genetics and Genomics
Microbiology
Microscopy
Molecular Sequence Data
oxygen
Phylogeny
polymerase chain reaction
Proteobacteria
Sequence Alignment
Studies
Vinegar
vinegars
Vitis - microbiology
title Cellulose production and cellulose synthase gene detection in acetic acid bacteria
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