Evidence map›Paper›PMID 39828416›Full record

ArticleJournal of food science2025

Role of protein and lipid oxidation in hardening of high-protein bars during storage.

Rachel B Dietrich, Lily Lincoln, Shima Momen, Benjamin B Minkoff, Michael R Sussman, Audrey L Girard

Abstract read
In one paragraph

Article in Journal of food science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Rachel B DietrichDepartment of Food Science, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Lily LincolnDepartment of Food Science, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Shima MomenDepartment of Food Science, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Benjamin B MinkoffCenter for Genomic Science Innovation, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Michael R SussmanCenter for Genomic Science Innovation, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Audrey L GirardDepartment of Food Science, University of Wisconsin-Madison, Madison, Wisconsin, USA.

Funding

ACQUISITION OF MASS SPECTROMETER FOR CORE FACILITYS10RR013790 · NCRR · UNIVERSITY OF WISCONSIN MADISON · PI RAINES, RONALD T · 1999 to 1999
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NCRR NIH HHS S10 RR013790Susan and Chris Salm Foundation S10RR13790Wisconsin Alumni Research Foundation BIR-9512577
6 · The paper itself

Abstract

Protein bar hardening negatively impacts shelf life, quality, and consumer acceptance. Although oxidation is known to negatively affect the flavor and texture of foods, the specific roles of lipid and protein oxidation in bar hardening have not been thoroughly investigated. Furthermore, most research has concentrated on dairy proteins, with a notable lack of studies addressing the hardening of plant-based protein bars. We investigated the role of protein and lipid oxidation, Maillard reactions, moisture loss, protein aggregation, and microstructural changes in the hardening of pea, whey, and rice protein bars over a storage period of 6 weeks (hardness increased 7.2×, 5.4×, and 4.4×, respectively). Changes in tryptophan fluorescence, free sulfhydryl content (e.g., loss of 57% for pea and 44% for whey), and carbonyl content demonstrated that pea and whey bars underwent protein oxidation. Lipid oxidation also occurred, demonstrated by increased peroxide and thiobarbituric acid-reactive substance values. Rice bars, however, did not undergo oxidation. Mass spectrometry indicated greater Maillard-reaction-related protein glycations formed in pea and whey bars (6.9% and 7.7%, respectively) than in rice bars (2.1%). SDS-PAGE revealed that pea and whey, but not rice, proteins aggregated during storage. Overall, this study found that moisture loss, protein and lipid oxidation, Maillard reactions, and protein aggregation correlated with bar hardening. Chemical changes may cause protein aggregation, resulting in hardening. Likely because of rice proteins' innate insolubility and disulfide linkages, rice protein bars were less susceptible to chemical changes and aggregation and hardened more slowly than whey and pea protein bars. PRACTICAL APPLICATION: This study shows that lipid and protein oxidation are correlated with protein bar hardening in both pea and whey protein bars. Additionally, this work suggests that rice protein bars may harden more slowly than pea and whey bars. These findings suggest that potential strategies to prevent bar hardening and extend shelf life include (1) adding antioxidants to prevent oxidation and (2) using rice proteins to partially or fully substitute other protein isolates.

Indexed as

Food StorageLipidsMaillard ReactionOryzaOxidation-ReductionPea ProteinsPisum sativumWhey ProteinsLipidsPea ProteinsWhey Proteinsbar hardeninglipid oxidationplant proteinprotein oxidation

Identifiers

PMID39828416
PMCPMC11743340

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.