Publication:
Use of Β-Cyclodextrin and Activated Carbon for Quantification of Salmonella Enterica Ser. Enteritidis from Ground Beef by Conventional Pcr

dc.contributor.advisorRobert E Levin
dc.contributor.authorOpet, Nathan J
dc.contributor.departmentUniversity of Massachusetts Amherst
dc.contributor.departmentFood Science
dc.date2023-09-23T08:14:18.000
dc.date.accessioned2024-04-26T20:37:34Z
dc.date.available2013-08-19T00:00:00Z
dc.date.issued2013-01-01
dc.date.submittedSeptember
dc.description.abstractFoods contaminated with pathogens are common sources of illness. Currently the most common and sensitive rapid detection methods involve the PCR. However, food matrices are complex and limit the sensitivity and thus detection limits. The use of coated activated carbon can effectively facilitate the removal of PCR inhibitors while not binding targeted bacterial cells from food samples. With activated carbon coated with the optimal amount of milk proteins a cell recovery at pH 7.0 of 95.7 ± 2.0% was obtained, compared to control uncoated activated carbon, which yielded a cell recovery of only 1.1 ± 0.8%. In addition, the milk protein coated activated carbon (MP-CAC) was able to absorb similar amounts of soluble compounds as uncoated activated carbon with the exception of bovine hemoglobin. This is evidence that the use of milk proteins to coat activated carbon should therefore serve as a suitable replacement for bentonite in the coating of activated carbon, which has previously been used for the removal of PCR inhibitors from food. The high amount of PCR inhibitors present in ground beef is a major factor that affects molecular based techniques such as the PCR for the detection of Salmonella enterica. In this study, a novel detection system was developed for eliminating PCR inhibitors and increasing the recovery of S. enterica in ground beef samples with the use of β-cyclodextrin and MP-CAC without enrichment of samples. invA, present in all Salmonella, was used as target the gene in the conventional PCR protocol. With ground beef containing 7.0, 15, and 27 % fat, treatment of stomached samples with 5.0, 10, and 15 % β-cyclodextrin respectively followed by treatment with MP-CAC, resulted in detection of 3 CFU/g which is equivalent to 75 CFU in 25 g samples. The total assay time was 4.5 hr. The methodology described in this study for the detection of S. enterica in ground beef without enrichment is rapid, sensitive, and has the potential to be applied to a number of food matrices to detect low numbers of food-borne bacterial pathogens before product is shipped to prevent costly recalls.
dc.description.degreeMaster of Science (M.S.)
dc.identifier.doihttps://doi.org/10.7275/4461341
dc.identifier.urihttps://hdl.handle.net/20.500.14394/44585
dc.relation.urlhttps://scholarworks.umass.edu/cgi/viewcontent.cgi?article=2253&context=theses&unstamped=1
dc.source.statuspublished
dc.subjectActivated carbon
dc.subjectβ-cyclodextrin
dc.subjectground beef
dc.subjectPCR
dc.subjectSalmonella
dc.subjectFood Science
dc.subjectMicrobiology
dc.titleUse of Β-Cyclodextrin and Activated Carbon for Quantification of Salmonella Enterica Ser. Enteritidis from Ground Beef by Conventional Pcr
dc.typecampus
dc.typearticle
dc.typethesis
digcom.contributor.authorisAuthorOfPublication|email:nopet@foodsci.umass.edu|institution:University of Massachusetts Amherst|Opet, Nathan J
digcom.date.embargo2013-08-19T00:00:00-07:00
digcom.identifiertheses/1145
digcom.identifier.contextkey4461341
digcom.identifier.submissionpaththeses/1145
dspace.entity.typePublication
Files
Original bundle
Now showing 1 - 2 of 2
No Thumbnail Available
Name:
Nathan_Opet_Thesis_2013.doc
Size:
2.04 MB
Format:
Microsoft Word
No Thumbnail Available
Name:
Nathan_Opet_Thesis_2013.pdf
Size:
2.03 MB
Format:
Adobe Portable Document Format
Collections