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<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/"><rdf:Description rdf:about="https://dk.um.si/IzpisGradiva.php?id=66997"><dc:title>16S rRNA in situ hybridization followed by flow cytometry for rapid identification of acetic acid bacteria involved in submerged industrial vinegar production</dc:title><dc:creator>Trček,	Janja	(Avtor)
	</dc:creator><dc:creator>Lipoglavšek,	Luka	(Avtor)
	</dc:creator><dc:creator>Avguštin,	Gorazd	(Avtor)
	</dc:creator><dc:subject>microbiology</dc:subject><dc:subject>acetic acid bacteria</dc:subject><dc:subject>flow cytometry</dc:subject><dc:description>Acetic acid bacteria are involved in many biotechnological processes such as vitamin C, gluconic acid, miglitol or acetic acid production, and others. For a technologist trying to control the industrial process, the ability to follow the microbiological development of the process is thus of importance. During the past few years hybridization in a combination with flow cytometry has oft en been used for this purpose. Since vinegar is a liquid, it is an ideal matrix for flow cytometry analysis. In this work we have constructed a specific probe for highly acetic acid-resistant species of the acetic acid bacteria and a protocol for in situ hybridization, which in combination with flow cytometry enables direct monitoring of bacteria producing vinegar with &gt;10 % of acetic acid. The approach was successfully applied for monitoring microbiota during industrial vinegar production.</dc:description><dc:publisher>University of Zagreb Faculty of Food Technology and Biotechnology </dc:publisher><dc:date>2016</dc:date><dc:date>2017-07-24 11:58:08</dc:date><dc:type>Znanstveno delo</dc:type><dc:identifier>66997</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>
