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Effects of Laccase and Transglutaminase on the Physicochemical and Functional Properties of Hybrid Lupin and Whey Protein Powder

aut.relation.endpage2090
aut.relation.issue13
aut.relation.journalFoods
aut.relation.startpage2090
aut.relation.volume13
dc.contributor.authorSantoso, Teguh
dc.contributor.authorHo, Thao M
dc.contributor.authorVinothsankar, Geerththana
dc.contributor.authorJouppila, Kirsi
dc.contributor.authorChen, Tony
dc.contributor.authorOwens, Adrian
dc.contributor.authorLazarjani, Masoumeh Pourseyed
dc.contributor.authorFarouk, Mustafa M
dc.contributor.authorColgrave, Michelle L
dc.contributor.authorOtter, Don
dc.contributor.authorKam, Rothman
dc.contributor.authorLe, Thao T
dc.date.accessioned2024-07-08T04:20:46Z
dc.date.available2024-07-08T04:20:46Z
dc.date.issued2024-07-01
dc.description.abstractPlant-based protein is considered a sustainable protein source and has increased in demand recently. However, products containing plant-based proteins require further modification to achieve the desired functionalities akin to those present in animal protein products. This study aimed to investigate the effects of enzymes as cross-linking reagents on the physicochemical and functional properties of hybrid plant- and animal-based proteins in which lupin and whey proteins were chosen as representatives, respectively. They were hybridised through enzymatic cross-linking using two laccases (laccase R, derived from Rhus vernicifera and laccase T, derived from Trametes versicolor) and transglutaminase (TG). The cross-linking experiments were conducted by mixing aqueous solutions of lupin flour and whey protein concentrate powder in a ratio of 1:1 of protein content under the conditions of pH 7, 40 °C for 20 h and in the presence of laccase T, laccase R, or TG. The cross-linked mixtures were freeze-dried, and the powders obtained were assessed for their cross-linking pattern, colour, charge distribution (ζ-potential), particle size, thermal stability, morphology, solubility, foaming and emulsifying properties, and total amino acid content. The findings showed that cross-linking with laccase R significantly improved the protein solubility, emulsion stability and foaming ability of the mixture, whereas these functionalities were lower in the TG-treated mixture due to extensive cross-linking. Furthermore, the mixture treated with laccase T turned brownish in colour and showed a decrease in total amino acid content which could be due to the enzyme’s oxidative cross-linking mechanism. Also, the occurrence of cross-linking in the lupin and whey mixture was indicated by changes in other investigated parameters such as particle size, ζ-potential, etc., as compared to the control samples. The obtained results suggested that enzymatic cross-linking, depending on the type of enzyme used, could impact the physicochemical and functional properties of hybrid plant- and animal-based proteins, potentially influencing their applications in food.
dc.identifier.citationFoods, ISSN: 2304-8158 (Online), MDPI AG, 13(13), 2090-2090. doi: 10.3390/foods13132090
dc.identifier.doi10.3390/foods13132090
dc.identifier.issn2304-8158
dc.identifier.urihttp://hdl.handle.net/10292/17756
dc.languageen
dc.publisherMDPI AG
dc.relation.urihttps://www.mdpi.com/2304-8158/13/13/2090
dc.rights© 2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
dc.rights.accessrightsOpenAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject0908 Food Sciences
dc.subject3006 Food sciences
dc.subject3106 Industrial biotechnology
dc.titleEffects of Laccase and Transglutaminase on the Physicochemical and Functional Properties of Hybrid Lupin and Whey Protein Powder
dc.typeJournal Article
pubs.elements-id559916

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