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Lactic acid bacteria and yeast heterogeneity during aerobic and modified atmosphere packaging storage of natural black Conservolea olives in polyethylene pouches

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dc.contributor.author Doulgeraki, AI en
dc.contributor.author Hondrodimou, O en
dc.contributor.author Iliopoulos, V en
dc.contributor.author Panagou, EZ en
dc.date.accessioned 2014-06-06T06:51:53Z
dc.date.available 2014-06-06T06:51:53Z
dc.date.issued 2012 en
dc.identifier.issn 09567135 en
dc.identifier.uri http://dx.doi.org/10.1016/j.foodcont.2012.01.006 en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/5756
dc.subject Black olives en
dc.subject Lactic acid bacteria en
dc.subject Modified atmosphere packaging en
dc.subject PFGE en
dc.subject RFLP en
dc.subject Yeasts en
dc.subject.other Bacilli (class) en
dc.subject.other Bacteria (microorganisms) en
dc.subject.other Lactobacillus en
dc.subject.other Lactobacillus pentosus en
dc.subject.other Lactobacillus plantarum en
dc.subject.other Oleaceae en
dc.subject.other Pichia en
dc.subject.other Pichia membranifaciens en
dc.title Lactic acid bacteria and yeast heterogeneity during aerobic and modified atmosphere packaging storage of natural black Conservolea olives in polyethylene pouches en
heal.type journalArticle en
heal.identifier.primary 10.1016/j.foodcont.2012.01.006 en
heal.publicationDate 2012 en
heal.abstract The yeast and lactic acid bacteria (LAB) community structure and dynamics was assessed during storage of Conservolea natural black olives in different modified atmospheres. Black olives were packed without brine in polyethylene pouches under air and modified atmospheres (20%CO 2-80%N 2 and 40%CO 2-30%O 2-30%N 2) and stored at 4 °C for a period of ca. 4 months. Yeast and LAB species diversity was evaluated before packaging, at the early (4 days), middle (77 days) and final (128 days) stages of storage. Yeast identification was based on restriction fragment length polymorphism and sequence analyses of the 5.8S internal transcribed spacer and the D1/D2 ribosomal DNA (rDNA) regions of isolates. Multiplex PCR amplification with recA gene derived primers was performed for the bacilli isolates for the differentiation of Lactobacillus plantarum group, while the remaining isolates were subjected to species identification by sequencing the V1-V3 variable region of the 16S rRNA gene. LAB heterogeneity at strain level was performed with Pulsed Field Gel Electrophoresis (PFGE). Analysis revealed a LAB community that composed of 5 species and 41 strains. The highest heterogeneity regarding strain frequency was observed for Lactobacillus pentosus with 20 strains, followed by L. plantarum with 9 strains. For yeasts, Pichia membranifaciens dominated in all pouches regardless of gas composition with frequency higher than 80% throughout storage. The composition of the modified atmosphere 20%CO 2-80%N 2 remained stable during storage. However, the presence of O 2 in the aerobic and 40%CO 2-30%O 2-30%N 2 pouches favoured the respiratory activity of yeasts resulting in a change in the initial gas composition with O 2 depletion and CO 2 accumulation. © 2012 Elsevier Ltd. en
heal.journalName Food Control en
dc.identifier.issue 1 en
dc.identifier.volume 26 en
dc.identifier.doi 10.1016/j.foodcont.2012.01.006 en
dc.identifier.spage 49 en
dc.identifier.epage 57 en


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