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Wheat germ oil (WGO) is rich in highly concentrated nutrients, especially vitamin E and polyunsaturated fatty acids. In this study, changes in oxidative stability, bioactive components, volatile compounds, and antioxidant capacity of WGO extracted from wheat germ roasted at 180 °C for 0–20 min were investigated. In general, antioxidant capacity and oxidative stability of WGO increased with roasting. Compared to oil from unroasted wheat germ, oil from wheat germ roasted for 20 min demonstrated the highest total phenolics, but a slight reduction in total tocopherols and β-carotenoids content. Fatty acid profiles were not affected, whereas hydroxymethylfrufural (HMF) content increased significantly, suggested the extent of Maillard reaction increased significantly with roasting. Among volatiles, esters such as n-butyl acrylate and acids such as hexanoic acid prevailed in WGO from unroasted wheat germ. However, after roasting, the levels of these compounds decreased or disappeared and furfurans, pyranes, pyrazines, and pyrroles with high odor activity became the most abundant.

With an interest to enhance the aroma of palm kernel oil (PKO), Pentopan mono BG (xylanase) was applied to alter the carbohydrates in palm kernels (PK) so as to modulate the formation of volatiles during kernel roasting. The result showed that a 1.3-fold increment of total soluble sugars was found in PK after Pentopan treatment, which promoted the generation of O-heterocyclic volatile compounds during kernel roasting. Overall, an increment of 1.5-, 1.4- and 1.3-fold of O-heterocyclic compounds were found in PKO derived from treated PK after light, medium and dark roasting, of which the elevation in furfural and 2-furanmethanol contents was the most obvious. Principal component analysis (PCA) clearly discriminated treated PKO with various kernel roasting degrees from that of control PKO on the basis of all aroma-active compounds; the aroma in PKO from treated, roasted PK was highly correlated with 2-[(methyldithio)methyl]-furan, 5-methyl-2-furancarboxaldehyde, 2-furanmethanol, 2,5-dimethylpyrazine and ethyl pyrazine. Sensory evaluation showed that PKO derived from medium roasted PK imparted more caramelic, nutty and smoky odor notes relative to the untreated PKO. This study suggests Pentopan pretreatment of PK followed by roasting may be a novel way to modulate PKO aroma and potentially widen its application.

Solid-state fermentation with Yarrowia lipolytica was applied to palm kernels (PK) with the aim to modulate the aroma of palm kernel oil (PKO) obtained after kernel roasting. The results showed that, the metabolic activities of Y. lipolityca brought about significant changes to the volatile profile of obtained PKO either by providing thermal reaction reactants or by directly contributing aroma compounds. After fermentation, a decreased content in glucose (60%) while an elevated amount (7-fold) in free amino acids was found in PK, which further impacted the formation of volatile compounds by influencing the Maillard reaction and Strecker degradation during roasting. More Strecker aldehydes and N-heterocyclic compounds were formed in PKO derived from fermented PK especially after intensified roasting. In addition, the catabolism of Y. lipolytica imparted some distinct volatile compounds such as 2-phenylethanol to the obtained PKO. However, the lipase excreted by Y. lipolytica hydrolysed PK lipids and released 5-fold more free fatty acids in fermented PKO, relative to the blank and control PKO, which likely contributed to the off-flavor. On the basis of all volatile categories, principal component analysis (PCA) clearly separated the fermented PKO from the blank and control PKO, with light roasted, fermented PKO being correlated with acids, alcohols and aliphatic aldehydes; medium and dark roasted, fermented PKO tending to be dominated by pyrroles, pyrazines and furanones, which is in correspondence with sensory changes of PKO. This study demonstrated that combining fermentation with roasting could provide a novel way to modulate the volatile composition and aroma of PKO.

Palm kernel oil (PKO) is obtained from the seeds of oil palm (Elaeis guineensis Jackqu). In this study, volatiles and aroma-active compounds of PKO were studied by head-space solid-phase microextraction/gas chromatography/mass spectrometry/flame ionisation detector (HS-SPME/GC/MS/FID) and solvent-assisted flavour evaporation -gas chromatography/olfactometry/mass spectrometry (SAFE-GC/O/MS), respectively. An optimised HS-SPME sampling method was obtained for extraction at 60 °C for 40 min. With this method, the volatiles of PKO from palm kernels subjected to different roasting times (up to 30 min) at 180 °C were analysed. Totally 73 volatiles were found, including 19 O-heterocyclic compounds (16 furans and 3 pyrans), 15 N-heterocyclic compounds (10 pyrazines and 5 others), 15 carbonyl compounds (5 aldehydes and 10 ketones), 11 acids, 4 alcohols, 3 esters, 3 sulphur and 3 volatile phenols. With the extension of roasting times, peak areas of O-heterocyclic compounds, N-heterocyclic compounds, aldehydes and cyclic ketones increased significantly whereas those of acids, alcohols and esters generally decreased. Results of GC/O/MS showed that 2-nonanone, octanoic acid and methyl octanoate were the most aroma-active compounds in unroasted PKO, while in roasted PKO, the most active volatiles were ethyl pyrazine, 2-nonanone, 2-hydroxy-3-methyl-2-cyclopenten-1-one, maltol, 2,6-dimethylpyrazine, 2,5-dimethylpyrazine, 2,3-dimethylpyrazine, benzoic acid ethyl ester, octanoic acid, 5-methyl-2-furancarboxaldehyde and isomaltol.

Wheat germ is a good source for wheat germ oil, and it is a by-product with highly concentrated nutrients from the wheat flour-milling industries. In the present study, raw wheat germ was firstly heat-treated at 180 °C for 20 min in a fluidized bed dryer, and further roasted at 180 °C for different periods of time. Roasting influence on total phenolic content (TPC), antioxidant activities, and phenolic compositions of wheat germ were evaluated. The roasting process significantly increased the TPC and antioxidant activities including free radical scavenging against DPPH and ABTS radicals, FRAP, and ORAC. In particular, the wheat germ roasted at 180 °C for 20 min showed higher antioxidant activity than those roasted at 180 °C for 5 and 10 min. Three major phenolic acids, namely, ferulic, chlorogenic, and caffeic acid, and four main flavonoids, namely, schaftoside and its isomers or adduct of sinapic acid were identified by HPLC. In general, the content of individual phenolic compounds decreased with prolongation of the roasting time except for ferulic acid. The results suggest that the antioxidant activities of wheat germ can be enhanced by roasting, and the enhancement effect might be partially attributed to the formation of Maillard reaction products (MRP).

With an interest to enhance the aroma of palm kernel oil (PKO), Viscozyme L, an enzyme complex containing a wide range of carbohydrases, was applied to alter the carbohydrates in palm kernels (PK) to modulate the formation of volatiles upon kernel roasting. After Viscozyme treatment, the content of simple sugars and free amino acids in PK increased by 4.4-fold and 4.5-fold, respectively. After kernel roasting and oil extraction, significantly more 2,5-dimethylfuran, 2-[(methylthio)methyl]-furan, 1-(2-furanyl)-ethanone, 1-(2-furyl)-2-propanone, 5-methyl-2-furancarboxaldehyde and 2-acetyl-5-methylfuran but less 2-furanmethanol and 2-furanmethanol acetate were found in treated PKO; the correlation between their formation and simple sugar profile was estimated by using partial least square regression (PLS1). Obvious differences in pyrroles and Strecker aldehydes were also found between the control and treated PKOs. Principal component analysis (PCA) clearly discriminated the treated PKOs from that of control PKOs on the basis of all volatile compounds. Such changes in volatiles translated into distinct sensory attributes, whereby treated PKO was more caramelic and burnt after aqueous extraction and more nutty, roasty, caramelic and smoky after solvent extraction.