Diversity and succession of microbial communities and chemical analysis in dried Lutianus erythropterus during storage

dc.contributor.authorDeng, Yijia
dc.contributor.authorWang, Rundong
dc.contributor.authorWang, Yaling
dc.contributor.authorSun, Lijun
dc.contributor.authorTao, Sen
dc.contributor.authorLi, Xuepeng
dc.contributor.authorGooneratne, R
dc.contributor.authorZhao, Jian
dc.coverage.spatialNetherlands
dc.date.accessioned2020-07-02T02:43:55Z
dc.date.available2019-11-01
dc.date.issued2020-02-02
dc.date.submitted2019-10-31
dc.description.abstractThe population, diversity and succession of microbial communities and chemical characteristics of dried crimson snapper (Lutianus erythropterus) during storage for 50 days were investigated. The population of bacteria, yeasts and filamentous fungi in the samples were enumerated by culture methods using appropriate agar media. The amplicons of the 16S rRNA of bacteria and the ITS region of fungi were sequenced and compared with gene libraries to obtain the identity and abundance of microorganisms in the community. Free amino acids and several other chemical characteristics were determined by HPLC and corresponding chemical reaction methods. Before storage, the average counts of bacteria, yeasts and filamentous fungi in the dried fish were 3.2, 2.5 and 2.2 log CFU/g, which increased to 4.6, 3.6 and 3.9 log CFU/g, respectively after storage. Major succession in the bacterial > fungal communities occurred during storage as evidenced by a significant decline in the number and diversity of microbial communities. Predominant bacterial genera were Phytobacteria, Vibrio, Acinetobacter and Macrococcus in the freshly dried fish, which were replaced by Bacillaceae, Halomonas, Lentibacillus, Alkalibacillus after storage. The fungal community of the freshly dried fish consisted of Penicillum > Yamadazyma, Malassezia, Candida and Eurotiales with Penicillum being the most dominant. Penicillium camemberti was the most abundant fungal species in the dried fish before storage with most dominant after storage and accounted for >96% of the abundance. The succession in the microbial community was accompanied by major changes in chemical characteristics with a significant decrease in fat, and an increase in total free amino acids and total volatile basic nitrogen (TVB-N).
dc.format.extent10 pages
dc.format.mediumPrint-Electronic
dc.identifierS0168-1605(19)30347-2
dc.identifierhttps://www.ncbi.nlm.nih.gov/pubmed/31707172
dc.identifier.doi10.1016/j.ijfoodmicro.2019.108416
dc.identifier.eissn1879-3460
dc.identifier.issn0168-1605
dc.identifier.other31707172 (pubmed)
dc.identifier.urihttps://hdl.handle.net/10182/12135
dc.languageen
dc.language.isoen
dc.publisherElsevier
dc.relationThe original publication is available from Elsevier - https://doi.org/10.1016/j.ijfoodmicro.2019.108416 - http://dx.doi.org/10.1016/j.ijfoodmicro.2019.108416
dc.relation.isPartOfInternational Journal of Food Microbiology
dc.relation.urihttps://doi.org/10.1016/j.ijfoodmicro.2019.108416
dc.rights© 2019 Elsevier B.V.
dc.subjectLutianus erythropterus
dc.subjectdried fish
dc.subjecthigh-throughput sequencing
dc.subjectmicrobial community
dc.subjectchemical changes
dc.subject.meshAnimals
dc.subject.meshFishes
dc.subject.meshBacteria
dc.subject.meshFungi
dc.subject.meshNitrogen
dc.subject.meshFats
dc.subject.meshAmino Acids
dc.subject.meshDNA, Ribosomal
dc.subject.meshFood Microbiology
dc.subject.meshFish Products
dc.subject.meshFood, Preserved
dc.subject.meshMicrobiota
dc.subject.meshAmino Acids
dc.subject.meshAnimals
dc.subject.meshBacteria
dc.subject.meshDNA, Ribosomal
dc.subject.meshFats
dc.subject.meshFish Products
dc.subject.meshFishes
dc.subject.meshFood Microbiology
dc.subject.meshFood, Preserved
dc.subject.meshFungi
dc.subject.meshMicrobiota
dc.subject.meshNitrogen
dc.titleDiversity and succession of microbial communities and chemical analysis in dried Lutianus erythropterus during storage
dc.typeJournal Article
lu.contributor.unitLincoln University
lu.contributor.unitFaculty of Agriculture and Life Sciences
lu.contributor.unitDepartment of Wine, Food and Molecular Biosciences
lu.identifier.orcid0000-0002-5406-2894
pubs.notesArticle ID 108416
pubs.publication-statusPublished
pubs.publisher-urlhttp://dx.doi.org/10.1016/j.ijfoodmicro.2019.108416
pubs.volume314
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