Establishment of ddPCR detection technology system for three contaminants in fermented milk

Detalhes bibliográficos
Autor(a) principal: ZHOU,Wei
Data de Publicação: 2022
Outros Autores: LI,Yong-Bo, ZHANG,Ya-Lun, LI,Xian, SHI,Guo-hua, YANG,Xiao-long
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Food Science and Technology (Campinas)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-20612022000101120
Resumo: Abstract Three typical contaminant bacteria, namely, Gluconobacter, Acetobacter, and Lactobacillus, were selected from fermented milk. The strong specific genes were screened as target sequences, and the droplet digital polymerase chain reaction (ddPCR) amplification system and reaction conditions were optimized. We established a ddPCR detection method for the three kinds of bacteria in fermented milk and then verified the specificity and sensitivity of the method. Absolute quantitative results were also analyzed. Results showed that ddPCR detection method for the three contaminants was specific and sensitive, and that the lowest detectable concentrations of Gluconobacter, Bacteroides, and Lactobacillus plantarum were 8.8 × 100 CFU/mL, 8.9 × 101 CFU/mL, and 9.6 × 101 CFU/mL, respectively. The relationship between the quantitative analysis results and ddPCR test results was good, proving the feasibility of ddPCR for absolute quantitative detection. This manuscript reports on establishment of a ddPCR detection system for three bacterial contaminants in fermented milk. The ddPCR detection system has efficient detection of targeted bacterial contaminants in fermented milks that can be valuable to the dairy industry in terms of preventing economic loss due to microbial spoilage and associated quality defects.
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spelling Establishment of ddPCR detection technology system for three contaminants in fermented milkdroplet digital polymerase chain reactionGluconobacterAcetobacterLactobacillusAbstract Three typical contaminant bacteria, namely, Gluconobacter, Acetobacter, and Lactobacillus, were selected from fermented milk. The strong specific genes were screened as target sequences, and the droplet digital polymerase chain reaction (ddPCR) amplification system and reaction conditions were optimized. We established a ddPCR detection method for the three kinds of bacteria in fermented milk and then verified the specificity and sensitivity of the method. Absolute quantitative results were also analyzed. Results showed that ddPCR detection method for the three contaminants was specific and sensitive, and that the lowest detectable concentrations of Gluconobacter, Bacteroides, and Lactobacillus plantarum were 8.8 × 100 CFU/mL, 8.9 × 101 CFU/mL, and 9.6 × 101 CFU/mL, respectively. The relationship between the quantitative analysis results and ddPCR test results was good, proving the feasibility of ddPCR for absolute quantitative detection. This manuscript reports on establishment of a ddPCR detection system for three bacterial contaminants in fermented milk. The ddPCR detection system has efficient detection of targeted bacterial contaminants in fermented milks that can be valuable to the dairy industry in terms of preventing economic loss due to microbial spoilage and associated quality defects.Sociedade Brasileira de Ciência e Tecnologia de Alimentos2022-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-20612022000101120Food Science and Technology v.42 2022reponame:Food Science and Technology (Campinas)instname:Sociedade Brasileira de Ciência e Tecnologia de Alimentos (SBCTA)instacron:SBCTA10.1590/fst.115721info:eu-repo/semantics/openAccessZHOU,WeiLI,Yong-BoZHANG,Ya-LunLI,XianSHI,Guo-huaYANG,Xiao-longeng2022-05-03T00:00:00Zoai:scielo:S0101-20612022000101120Revistahttp://www.scielo.br/ctaONGhttps://old.scielo.br/oai/scielo-oai.php||revista@sbcta.org.br1678-457X0101-2061opendoar:2022-05-03T00:00Food Science and Technology (Campinas) - Sociedade Brasileira de Ciência e Tecnologia de Alimentos (SBCTA)false
dc.title.none.fl_str_mv Establishment of ddPCR detection technology system for three contaminants in fermented milk
title Establishment of ddPCR detection technology system for three contaminants in fermented milk
spellingShingle Establishment of ddPCR detection technology system for three contaminants in fermented milk
ZHOU,Wei
droplet digital polymerase chain reaction
Gluconobacter
Acetobacter
Lactobacillus
title_short Establishment of ddPCR detection technology system for three contaminants in fermented milk
title_full Establishment of ddPCR detection technology system for three contaminants in fermented milk
title_fullStr Establishment of ddPCR detection technology system for three contaminants in fermented milk
title_full_unstemmed Establishment of ddPCR detection technology system for three contaminants in fermented milk
title_sort Establishment of ddPCR detection technology system for three contaminants in fermented milk
author ZHOU,Wei
author_facet ZHOU,Wei
LI,Yong-Bo
ZHANG,Ya-Lun
LI,Xian
SHI,Guo-hua
YANG,Xiao-long
author_role author
author2 LI,Yong-Bo
ZHANG,Ya-Lun
LI,Xian
SHI,Guo-hua
YANG,Xiao-long
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv ZHOU,Wei
LI,Yong-Bo
ZHANG,Ya-Lun
LI,Xian
SHI,Guo-hua
YANG,Xiao-long
dc.subject.por.fl_str_mv droplet digital polymerase chain reaction
Gluconobacter
Acetobacter
Lactobacillus
topic droplet digital polymerase chain reaction
Gluconobacter
Acetobacter
Lactobacillus
description Abstract Three typical contaminant bacteria, namely, Gluconobacter, Acetobacter, and Lactobacillus, were selected from fermented milk. The strong specific genes were screened as target sequences, and the droplet digital polymerase chain reaction (ddPCR) amplification system and reaction conditions were optimized. We established a ddPCR detection method for the three kinds of bacteria in fermented milk and then verified the specificity and sensitivity of the method. Absolute quantitative results were also analyzed. Results showed that ddPCR detection method for the three contaminants was specific and sensitive, and that the lowest detectable concentrations of Gluconobacter, Bacteroides, and Lactobacillus plantarum were 8.8 × 100 CFU/mL, 8.9 × 101 CFU/mL, and 9.6 × 101 CFU/mL, respectively. The relationship between the quantitative analysis results and ddPCR test results was good, proving the feasibility of ddPCR for absolute quantitative detection. This manuscript reports on establishment of a ddPCR detection system for three bacterial contaminants in fermented milk. The ddPCR detection system has efficient detection of targeted bacterial contaminants in fermented milks that can be valuable to the dairy industry in terms of preventing economic loss due to microbial spoilage and associated quality defects.
publishDate 2022
dc.date.none.fl_str_mv 2022-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-20612022000101120
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-20612022000101120
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/fst.115721
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Ciência e Tecnologia de Alimentos
publisher.none.fl_str_mv Sociedade Brasileira de Ciência e Tecnologia de Alimentos
dc.source.none.fl_str_mv Food Science and Technology v.42 2022
reponame:Food Science and Technology (Campinas)
instname:Sociedade Brasileira de Ciência e Tecnologia de Alimentos (SBCTA)
instacron:SBCTA
instname_str Sociedade Brasileira de Ciência e Tecnologia de Alimentos (SBCTA)
instacron_str SBCTA
institution SBCTA
reponame_str Food Science and Technology (Campinas)
collection Food Science and Technology (Campinas)
repository.name.fl_str_mv Food Science and Technology (Campinas) - Sociedade Brasileira de Ciência e Tecnologia de Alimentos (SBCTA)
repository.mail.fl_str_mv ||revista@sbcta.org.br
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