Evidence map›Paper›PMID 42828259›Full record

ArticleFood chemistry: X2026

Modulation of Maillard reaction pathways and aroma profiles in peanut oil using enzymatically tailored peanut meal hydrolysates.

Ming Yang, Jing Wang, Haiming Shi, Yanlan Bi, Xuebing Xu

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Article in Food chemistry: X, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Ming YangCollege of Food Science and Technology, Henan University of Technology, Zhengzhou 450001, China.
Jing WangWilmar (Shanghai) Biotechnology Research and Development Center Co., Ltd., Pudong New District, Shanghai 200137, China.
Haiming ShiWilmar (Shanghai) Biotechnology Research and Development Center Co., Ltd., Pudong New District, Shanghai 200137, China.
Yanlan BiCollege of Food Science and Technology, Henan University of Technology, Zhengzhou 450001, China.
Xuebing XuCollege of Food Science and Technology, Henan University of Technology, Zhengzhou 450001, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study establishes a mechanistic framework for directing Maillard-driven aroma formation in peanut oil through targeted enzymatic precursor engineering, exploring the potential of precursor engineering for flavor modulation in peanut oil. Defatted peanut meal was subjected to selective hydrolysis using distinct glycosidases (cellulase, hemicellulase, pectinase, α-amylase, and amyloglucosidase) in combination with proteases to systematically reconstruct the precursor microenvironment (reducing sugars and free amino acids). The resulting hydrolysates were thermally reacted with cold-pressed peanut oil at 120 °C, and the evolution of volatile profiles and sensory attributes was evaluated using an integrated sensory-directed flavoromics approach. Two enzymatic strategies, pectinase-protease and α-amylase-protease, emerged as highly effective in reprogramming Maillard pathways. These treatments generated a substantial expansion of key precursors, particularly glucose (up to >60-fold increase) and branched-chain amino acids, which were associated with selective formation of pyrazines and furan derivatives associated with roasted, savory, and caramel notes. Concurrently, lipid-derived off-flavor compounds such as hexanal and 1-octen-3-ol were significantly suppressed, indicating a possible shift in reaction dominance from lipid oxidation to Maillard chemistry. Correlation and network analyses revealed the precursor-volatile-sensory linkages, suggesting that specific precursor compositions (e.g., glucose-leucine-lysine systems) are associated with distinct aroma profiles. Notably, pentose-rich systems were associated with furan pathway activation, whereas hexose-dominant systems were associated with pyrazine formation. These findings provide evidence that enzyme-tailored precursor engineering can influence Maillard reaction pathways in edible oils in a potentially tunable manner, offering a promising strategy for producing peanut oil with tailored flavor profiles and suggesting potential improvements in oxidative stability.

Indexed as

ChemometricsEnzymatic pretreatmentMaillard reactionPeanut oilRelative odor activity valueSensory analysisVolatile compounds

Identifiers

PMID42828259
PMCPMC13632089

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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.