dc.contributor.author | Onifade, J.O. |
dc.date.accessioned | 2022-12-01T07:43:39Z |
dc.date.available | 2022-12-01T07:43:39Z |
dc.date.issued | 2022-03 |
dc.identifier.citation | Onifade, J.O. (2022). Rapid detection of adulterated fermented maize (Ogi) with sorghum leaf sheath (Poroporo) using visible-near infrared spectroscopy. Ibadan: University of Ibadan (86 p.). |
dc.identifier.uri | https://hdl.handle.net/20.500.12478/7944 |
dc.description.abstract | Food adulteration is a very old and common problem, which is often seen in both the low-and middle-income countries and even in some developed countries. Maize-based porridge especially ogi is a high-value commodity and common indigenous complementary food that is a target for adulteration, leading to loss of quality and encroachment on the rights and interests of consumers. This study investigated the characterization of the microorganisms found in ogi fermented for 0 to 120 hours and the feasibility of using visible - near Infrared (VIS-NIR) spectroscopy combined with multivariate analysis for detection and quantification of ogi adulterated with sorghum leaf sheath extract at different concentrations. NIR spectra of the adulterated and pure ogi were measured between the regions 400 – 2498 nm. The multivariate methods included Principal component analysis (PCA), multiplicative scatter correction (MSC), Savitzky-Golay derivatization, and partial least square – discriminant analysis (PLS-DA). PCA gave visible cluster trends for authentic samples and adulterated ones. PLS-DA was used to detect the discrimination between the pure and adulterated ogi samples. The PLS-DA model with MSC and fist derivative Savitzky-Golay normalization with five smoothing points was able to cross validate adulteration better at 5% adulteration level successfully compared to other adulteration levels. Standard microbiological characterization of the isolates conducted and results revealed that Saccharomyces cerevisiae, Candida and Lactobacillus species were the main microorganisms found in the fermentation medium within 96 hours of fermentation. There was an increase in the population of the bacteria and yeasts (measured in CFU ml-1) as the fermentation progressed. The results suggested that the predominant microorganisms during the fermentation period was the LABs and that NIR spectroscopy associated with multivariate analysis has the great potential for a rapid and non-destructive detection of adulteration in maize gruel (ogi). |
dc.format.extent | 86 p. |
dc.language.iso | en |
dc.publisher | University of Ibadan |
dc.subject | Food Security |
dc.subject | Maize |
dc.subject | Food Systems |
dc.subject | Processing |
dc.title | Rapid detection of adulterated fermented maize (Ogi) with sorghum leaf sheath (Poroporo) using visible-near infrared spectroscopy |
dc.type | Thesis |
cg.contributor.affiliation | University of Ibadan |
cg.contributor.affiliation | International Institute of Tropical Agriculture |
cg.coverage.region | Africa |
cg.coverage.region | West Africa |
cg.coverage.country | Nigeria |
cg.coverage.hub | Headquarters and Western Africa Hub |
cg.identifier.bibtexciteid | ONIFADE:2022 |
cg.authorship.types | CGIAR and developing country institute |
cg.iitasubject | Food Security |
cg.iitasubject | Food Systems |
cg.iitasubject | Maize |
cg.iitasubject | Plant Production |
cg.iitasubject | Post-Harvesting Technology |
cg.iitasubject | Value Chains |
cg.notes | IITA supervisor: Dr. Falade, T. |
cg.publicationplace | Ibadan, Nigeria |
cg.accessibilitystatus | Limited Access |
cg.reviewstatus | Internal Review |
cg.usagerightslicense | Copyrighted; all rights reserved |
cg.targetaudience | Scientists |
cg.futureupdate.required | No |
cg.contributor.acknowledgements | First and foremost, my gratitude goes to God Almighty for His grace that was so sufficient, without it this work would not have been possible.
My special gratitude to my supervisors Dr. Kolawole Banwo and co-supervisor Dr. Titilayo Falade for providing invaluable scholarly comments, guidance and support that greatly shaped my research work, and for creating time to read this work at different stages despite their busy schedules. I also wish to thank all the members of Aflasafe and Pathology Laboratory of International Institute of Tropical Agriculture (IITA) for their invaluable input and insightful comments that were implemented to improve the document. I am also grateful to University of Ibadan for according me the opportunity to do my masters and giving me the support needed to complete the study.
Many thanks to all my colleagues especially Kayode-Oni Somi, Tomi, Tobi, Kingsley, for their love and support in various ways to produce this work.
I am greatly indebted to all members of my family, my parents my brothers and sister who were a source of inspiration. Kindly receive my appreciation. My gratitude greatly falls on my brother from another mother, Rev. Fr. Dominic Olagbaju, for supporting me in all aspects of life, inculcating the love for education in me, for his concern and for always being there for me.
Thank you. |