Volatile Formation Research Articles

Cellulose pyrolysis via liquid metal catalysis

Liquid metals are largely unexplored as catalytic media for biomass conversion. Unlike conventional solid-state catalysts which are prone to deactivation, liquid metals, i.e., low-melting metals operated above their melting point, can show resilience against coking, high thermal conductivity, and enhanced liquid-solid contact between catalyst and biomass feedstocks. This promise motivated the present investigation of liquid metals as catalysts for cellulose pyrolysis. Bismuth, tin, and indium were selected as liquid metal candidates, and their impact on cellulose devolatilization kinetics is studied via thermogravimetric analysis. The results indicate that all three metals show catalytic activity, with bismuth catalyzing volatiles formation, while indium and tin enhance char formation. Quantitative analysis of liquid product reveals that bismuth is selective to dehydration and functional rearrangement reactions, leading to anhydro sugars and functionalized furans formation. In contrast, indium and tin are selective towards dehydration, fragmentation reactions, and Diels Alder chemistry, leading to formation of C2-C4 fragments and aromatic compounds, as further confirmed via infrared spectroscopic analysis of the obtained chars. Finally, the Sn and Bi liquid metals’ stability against deactivation via coking is examined against conventional solid-state zeolite catalyst through multiple cellulose pyrolysis runs in the thermogravimetric analyzer (TGA) with the same batch of catalyst. While ZSM-5 zeolite catalyst's activity and selectivity declined and approached non-catalytic sand results (both the TGA curve and the liquid product distribution) within the first few runs, both Sn and Bi fairly maintained their robustness against coking for the conducted durability runs. Overall, the results show significant promise for this new class of catalysts for biomass pyrolysis.

Structure, mechanical, and tribological properties of Ag2CrO4 high-temperature oxide coatings

In this research, a series of Ag2CrO4 high-temperature self-lubricating oxide coatings were prepared by reactive radio frequency magnetron sputtering under different argon-oxygen flow ratio (Ar:O2 ratio) conditions. Effects of the gas flow ratio on phase composition, coating morphology, high temperature treatment in air atmosphere, mechanical and tribological properties are studied. A low Ar:O2 flow ratio is beneficial for the formation of Ag2CrO4 phase. At high temperature treatment, formation of surface Ag particle and volatility and decomposition of the Ag2CrO4 phase are observed, and the volatility and decomposition of the coating are slight at temperatures below 500 °C. When the Ar:O2 ratio is 1:1, the coating shows exceptional comprehensive performance, it is dense with a smooth surface, excellent toughness and bond strength, and the lowest wear rate and coefficient of friction, which is 0.14 mm3/10−3N∙m and 0.35 respectively. The coating can function as a lubricant in temperature environments of 500 ℃ and below, demonstrating practical application value.

Influence of the malting conditions on the modification and variation in the physicochemical properties and volatile composition of barley (Hordeum vulgare L.), rye (Secale cereale L.), and quinoa (Chenopodium quinoa Willd.) malts

The traditional malted cereal used primarily for beverages is barley (Hordeum vulgare L.), while rye (Secale cereale L.) is mainly used in baked goods. In contrast, quinoa (Chenopodium quinoa Willd.) is a gluten-free pseudocereal, rich in starch and high-quality proteins, that can be used similarly to cereals. Their physicochemical properties and volatile compositions (e.g., aroma compounds) directly influence the finished food products. The sharp bitterness of unprocessed rye and the earthy aroma of native quinoa can interfere with the development and acceptance of food products. Malting is known to improve the processing and sensory properties of barley. A face-centered, central composite design was used to investigate the individual and interactive effects of three malting parameters (i.e., steep moisture (SM), germination temperature (T), and germination time (t)) on malt quality indicators (e.g., extract) and volatile formation (e.g., 3-methylbutanal) in rye and quinoa, and were compared to barley. The malt modification predictive models were then used to determine standard malting regimes for brewing quality malts. The malting parameters for the steeping and germination stages were: 43 %, 15 °C, and 6 d for barley; 45 %, 12 °C, and 8 d for rye; and 46 %, 16 °C, 6 d for quinoa. Malt modification and volatile formation were primarily associated with the interactive effect of germination temperature and time. Conversely, steep moisture had limited impact on malt modification but strongly regulated the formation of 34 known (pseudo)cereal volatile compounds. Principal component analysis (PCA) of the volatile data identified (pseudo)cereal specific volatile patterns. Aldehydes were characteristic in the cereal malts, particularly barley, whereas phenyl compounds and pyrazines were abundant in rye and quinoa malts, respectively. Controlling (pseudo)cereal modification and volatile development through the malting process could help deliver targeted sensory properties and improve the acceptance of malt-based food products.

Targeted metabolomics reveals the contribution of degradation and oxidation of lipids and proteins mediated by pH to the formation of characteristic volatiles in preserved egg yolk during pickling

Targeted metabolomics and flavouromics combined with relative odor activity value were performed to explore the effect of degradation and oxidation of matrix mediated by pH on the formation of characteristic volatiles in preserved egg yolk (PEY) during pickling. It was found that the oxidation of proteins and lipids in PEY induced by pH sequentially occurred in early and later periods, and degradation both mainly occurred in early stage. Moreover, 1-octen-3-one, heptanal, trimethylamine, etc., compounds and 5-HETrE, proline, etc., components were confirmed as up-regulated characteristic volatiles and differential metabolites in PEY during pickling. The formation of octanal-M/D and benzeneacetaldehyde-M was attributed to β-oxidation of hydroxyeicosapentaenoic acid and L-isoleucine catalyzed by strong alkali at early period based on correlation network between them, respectively. Meanwhile, the generation of 1-octen-3-one-M/D mainly depended on L-serine and could be promoted by phosphatidylcholines oxidation. At later stage, the formation of heptanal-M/D was primarily attributed to phosphatidylethanolamines oxidation induced by alkali, and the enrichment of heptanal-M/D and nonanal were both enhanced by oxidized lipids. Lastly, trimethylamine was derived from L-lysine under alkaline conditions and promoted by protein oxidation during the whole process. This manuscript provided insight into the differential contribution of oxidation and degradation from matrix regulated by exogenous factors on the formation pathway for characteristic volatiles in foods.

Revealing the microbial diversity and volatile flavor formation in finger citron kombucha by metagenomic and GC-MS analysis

Kombucha is a kind of health drink formed by the metabolism of Symbiotic Culture of Bacteria and Yeast (SCOBY) composed of yeast, acetic acid bacteria and lactic acid bacteria, which is popular among researchers and fond of consumers because of its antioxidant and hypoglycemic effects. In this study, the finger citron kombucha with different fermentation time (2, 4, 6, 8 day) were analyzed by headspace solid phase micro-extraction gas chromatography-mass spectrometry (HS-SPME-GC-MS) and metagenomic sequencing. The results showed that a total of 76 volatiles were identified, including 15 key volatiles, such as linalool, geraniol, α-terpinene, and limonene, which had a great influence on the flavor of kombucha. Metagenomic analysis showed that unclassified-g-Gluconobacter, Komagataeibacter saccharivorans, Gluconobacter-sp.-R71656 and other microorganisms were the dominant species in finger citron kombucha. Through the correlation heat map analysis of volatiles and microbial composition, it was found that Gluconobacter had a positive effect on the formation of most volatiles of kombucha. In addition, Novacetimonas hansenii, Brettanomyces bruxellensis and Wickerhamiella sorbophila were also closely related to the flavor formation of kombucha. This study provided a theoretical basis for finding the key aroma-producing microorganisms in the fermentation process of finger citron kombucha and the subsequent construction of SCOBY.

The impacts of cold plasma on the taste and odor formation of dried silver carp products

This study investigated non-thermal pretreatment (cold plasma, CP) on the flavor (taste and odor) profiles of dried fish products. CP treatment of 5 min contributed to accumulation of umami nucleotides adenosine 5′-monophosphate (AMP) from 30.96 to 40.82 μg/g and inosine 5′-monophosphate (IMP) from 2009.29 to 2132.23 μg/g, and significant reduction of bitter hypoxanthine ribonucleoside (HxR) and hypoxanthine (Hx), respectively (P < 0.05) in the dried fish products. A noticeable enhancement in sweet glycine (from 429.41 to 490.03 mg/100 g) and umami glutamic acid (from 55.68 to 67.76 mg/100 g) accompanied with the CP treatment (P < 0.05) based on taste activity value (TAV > 1). And the characteristic odor volatiles (nonanal, hexanal and 1-octen-3-ol) were strengthened 2.13-, 2.16- and 2.17- folds, respectively (P < 0.05). The results of equivalent umami concentration and Gibbs free energy calculation, combining with the correlation analysis, indicate that nucleotides and free amino acids synergically enhanced the taste improvement of dried fish products. Moderate lipids oxidation favored the formation of characteristic volatiles. The CP pretreatment offered new strategies for enhancing flavor of dried fish products.

Lipid and volatile profiles of Finnish oat batches of pure cultivars: Effect of storage on the volatile formation

Recent data showing the compositional variation and storage behavior among different oat batches for the purpose of food remains limited. Lipids of twenty oat flour samples of pure cultivars grown in Finland during 2019 were extracted and fractionated into neutral and polar-rich lipids. Flour was stored for nine months, and profiles of volatiles and tocols were analyzed to reveal oxidative stability. The lipid content was 5.9–8.9 g per 100 g of flour [DW] and consisted of 78.7 ± 2.5 % neutral and 21.3 ± 2.5 % polar lipids. Palmitic (16 %), oleic (36 %), and linoleic (39 %) acids were the most abundant fatty acids. Neutral lipids had more oleic and less linoleic and palmitic acids than polar lipids. The fresh samples correlated with tocols, pentanal, 2-pentylfuran, 2-heptanone, nonanal, 2-butanone, and heptanal, while stored samples were associated with 3-octen-2-one, 2-octenal, hexanal, and octanal. Lipid composition and oxidative stability are essential factors for selecting oat batches for food applications.

Optimizing directed energy deposition of polymers through melt pool temperature control: impact on physical properties of polyamide 12 parts

The method of Directed Energy Deposition of polymers (DED-LB/P) was extended to allow control over the melt pool temperature using a pyrometer. DED-LB/P was used to build test specimen of polyamide 12 (PA12), orthogonal and parallel to the long side. Samples prepared under temperature control show superior mechanical properties over those generated without. The temperature of the melt pool allows to tune the quality of the built part. A too low temperature leads to a porous part on account of insufficient powder fusion, and a too high temperature leads to holes by formation of volatiles. The mechanical properties can be related to the porosity, the molecular mass of PA12 did not change substantially, the distribution width however increased with temperature. The best processing conditions were at 220 °C leading to a build part with a porosity of 0.6%, a Youngs modulus of 550 MPa and a fracture-strain of 15% with an ultimate strength of almost 28 MPa.

Analysis of root volatiles and functional characterization of a root-specific germacrene A synthase in Artemisia pallens.

The study demonstrated that Artemisia pallens roots can be a source of terpene-rich essential oil and root-specific ApTPS1 forms germacrene A contributing to major root volatiles. Davana (Artemisia pallens Bess) is a valuable aromatic herb within the Asteraceae family, highly prized for its essential oil (EO) produced in the aerial parts. However, the root volatile composition, and thegenes responsible for root volatiles have remained unexplored until now. Here, we show that A. pallens roots possess distinct oil bodies and yields ~ 0.05% of EO, which is primarily composed of sesquiterpenes β-elemene, neryl isovalerate, β-selinene, and α-selinene, and trace amounts of monoterpenes β-myrcene, D-limonene. This shows that, besides aerial parts, roots of davana can also be a source of unique EO. Moreover, we functionally characterized a terpene synthase (ApTPS1) that exhibited high in silico expression in the root transcriptome. The recombinant ApTPS1 showed the formation of β-elemene and germacrene A with E,E-farnesyl diphosphate (FPP) as a substrate. Detailed analysis of assay products revealed that β-elemene was the thermal rearrangement product of germacrene A. The functional expression of ApTPS1 in Saccharomyces cerevisiae confirmed the in vivo germacrene A synthase activity of ApTPS1. At the transcript level, ApTPS1 displayed predominant expression in roots, with significantly lower level of expression in other tissues. This expression pattern of ApTPS1 positively correlated with the tissue-specific accumulation level of germacrene A. Overall, these findings provide fundamental insights into the EO profile of davana roots, and the contribution of ApTPS1 in the formation of a major root volatile.

Integrated transcriptomics and metabolomics analysis provides insights into aromatic volatiles formation in Cinnamomum cassia bark at different harvesting times.

Cinnamomum cassia Presl, classified in the Lauraceae family, is widely used as a spice, but also in medicine, cosmetics, and food. Aroma is an important factor affecting the medicinal and flavoring properties of C. cassia, and is mainly determined by volatile organic compounds (VOCs); however, little is known about the composition of aromatic VOCs in C. cassia and their potential molecular regulatory mechanisms. Here, integrated transcriptomic and volatile metabolomic analyses were employed to provide insights into the formation regularity of aromatic VOCs in C. cassia bark at five different harvesting times. The bark thickness and volatile oil content were significantly increased along with the development of the bark. A total of 724 differentially accumulated volatiles (DAVs) were identified in the bark samples, most of which were terpenoids. Venn analysis of the top 100 VOCs in each period showed that twenty-eight aromatic VOCs were significantly accumulated in different harvesting times. The most abundant VOC, cinnamaldehyde, peaked at 120 months after planting (MAP) and dominated the aroma qualities. Five terpenoids, α-copaene, β-bourbonene, α-cubebene, α-funebrene, and δ-cadinene, that peaked at 240 MAP could also be important in creating C. cassia's characteristic aroma. A list of 43,412 differentially expressed genes (DEGs) involved in the biosynthetic pathways of aromatic VOCs were identified, including phenylpropanoids, mevalonic acid (MVA) and methylerythritol phosphate (MEP). A gene-metabolite regulatory network for terpenoid and phenylpropanoid metabolism was constructed to show the key candidate structural genes and transcription factors involved in the biosynthesis of terpenoids and phenylpropanoids. The results of our research revealed the composition and changes of aromatic VOCs in C. cassia bark at different harvesting stages, differentiated the characteristic aroma components of cinnamon, and illuminated the molecular mechanism of aroma formation. These foundational results will provide technical guidance for the quality breeding of C. cassia.

Research on the Influence of Microeconomic Factors on Stock Market Fluctuation

Market volatility has always been a focus of attention for investors and practitioners, as it is crucial for investment decision-making and risk management. Microeconomic factors, such as company financial conditions, macroeconomic factors, industry characteristics, and government policies, are considered to play a crucial role in the formation of stock market volatility. The contribution of this article lies in the in-depth exploration of the impact mechanism of microeconomic factors on stock market volatility, providing investors with more information on how to evaluate risks and formulate investment strategies. In addition, the research findings of this article can also guide financial practitioners to improve risk management tools and strategies to better adapt to market volatility. Governments and regulatory agencies can also develop more precise financial market policies based on research results to maintain market stability and fairness. In summary, this article emphasizes the importance of microeconomic factors in stock market volatility and provides in-depth insights on this key issue. This has important guiding significance for investment decision-making, risk management, and policy formulation in the financial field.

Characterization of the formation of key flavor volatiles in kiwifruit (Actinidia deliciosa) during storage by integrating

Characterization of the formation of key flavor volatiles in kiwifruit (Actinidia deliciosa) during storage by integrating

Multi-omics revealed the formation mechanism of characteristic volatiles in Tibetan yak cheese induced by different altitudes

The variation in volatiles, bacteria and metabolites of Tibetan yak cheese (TYC) from different altitudes were characterized with multi-omics to reveal the formation mechanism of characteristic volatile compounds (C-VOCs) in TYC induced by altitudes. 22C-VOCs (odor activity value, OAV > 1) were identified in TYCs, and hexanal, dodecanol, 2,3-butanediol, butyl isobutyate, etc., C-VOCs were confirmed induced by altitude. Lactobacillus, Kocuria, etc., bacteria and benzyl thiocyanate, trehalose, sarcosine, etc., metabolites were screened as the variable bacteria and metabolites for TYCs regulated by altitude, respectively. Pediococcus and carbonhydrates maybe the main contributors for the formation of C-VOCs in TYCs induced by altitudes. The formation of dodecanol, 2,3-butanediol and hexanal maybe derived from sarcosine and EPA, and the generation of butyl isobutyrates maybe originated from 1,6-DP-fructose and threonic acid facilitating by Pediococcus. This research will help us gain insight into the contribution of altitude to the formation of volatiles in TYCs.

Cellulose pyrolysis kinetic model: Detailed description of volatile species

Lignocellulosic biomass is typically composed by a major fraction of cellulose. Its decomposition influences on large extent the biomass rate of pyrolysis and product distribution, affecting process behaviour in thermochemical conversion processes. Containing approximately 90 % of volatile matter, volatile products from cellulose pyrolysis are very important in the characteristics of flames and ignition properties. Recent developments in analytical methods allowed a detailed identification of these volatile products, giving valuable information to process development and better understanding of kinetics. Predictions of a previous kinetic model are compared with these new findings, revealing large space for improvements. In this work, we propose a multi-step kinetic model of cellulose pyrolysis, incorporating the most recent experimental findings into the detailed product description. The model consists of four main reactions for the decomposition of cellulose, with formation of gases, volatiles, char and metaplastic species. The release of metaplastic species is described by a set of six reactions. The formation and release of 13 oxygenated hydrocarbons is predicted by the model, including anhydrosugars, furans, aldehydes, alcohols, ketones and carboxylic acids. The model also describes the formation of levoglucosan in metaplastic state before its release, explaining high heating rate mass loss behaviour. The model is compared with a large variety of experiments from literature, and validated for mass loss rates and product distribution, achieving overall good agreement despite experimental uncertainties and the large simplifications characteristic of the model formulation. Besides effectively quantifying the yields of gaseous, condensable and solid products, the model accurately captures the distribution of volatiles in terms of functional groups and C-chain length.

A comparative study to investigate the individual contribution of metabolic and physical interaction on volatiles formation in the mixed fermentation of Torulaspora delbrueckii and Saccharomyces cerevisiae

It is well-known that the co-inoculation of Saccharomyces cerevisiae and non-Saccharomyces strains can modulate and improve the aromatic quality of wine through their multi-level interactions. However, the individual contribution of metabolic interaction (MI) and physical interaction (PI) on wine volatiles remains poorly understood. In this work, we utilized a double-compartment bioreactor to examine the aromatic effect of MI and PI by comparing the volatiles production in Torulaspora delbrueckii and Saccharomyces cerevisiae single fermentations to their mixed fermentations with or without physical separation. Results showed that the PI between T. delbrueckii and S. cerevisiae increased the production of most aroma compounds, especially for acetate esters and volatile fatty acids. In comparison, the MI only promoted a few volatile compounds, including ethyl decanoate, isoamyl acetate, and isobutanol. Noticeably, the MI significantly decreased the levels of ethyl dodecanoate, 2-phenylethyl alcohol, and decanoic acid, which exhibited opposite profiles in PI. Our results indicated that the PI was mainly responsible for the improved volatiles in T. delbrueckii/S. cerevisiae mixed fermentation, while the MI can be targeted to modulate the specific aroma compounds. A thorough understanding of the PI and MI aromatic effect will empower winemakers to accurately and directionally control the volatile profile of the wine, promoting the application of multi-starters to produce diverse styles of wines.

Combining with volatilomic profiling and chemometrics to explore the volatile characteristics in five different dried Zanthoxylum bungeanum maxim

Owing to the short picking period of the fresh Zanthoxylum bungeanum, the postharvest drying has become an essential operation before the storage and transportation of Z. bungeanum. To explore the effects of drying methods on volatile characteristics, the volatilomic profiling of five different dried Z. bungeanum was investigated by E-nose, HS-SPME-GC/MS, GC-IMS in combination with chemometrics. The results indicated that W1W, W2W and W5S sensors within E-nose analysis showed the strongest responses in both fresh and dried Z. bungeanum. According to the identification of volatile organic compounds (VOCs), terpenes, esters and alcohols played the major roles in the volatile formation of the fresh and dried Z. bungeanum. The samples derived from hot air drying showed the relatively similar features with the fresh sample based on the relative abundances of these major VOCs. According to the results of multiple factor analysis (MFA), GC-IMS showed the strongest ability in distinguishing the fresh and different dried samples. Compared with the high levels of terpenes in fresh group, the significant increasement of terpene alcohols and terpene esters from the degradation and transformation of bound terpenoids was the main characteristics of all dried Z. bungeanum. Using the GC-IMS datasets, a weighted correlation network analysis (WCNA) model was constructed to clarify the VOC characteristics in all detetected samples. Thereinto, 6 significantly correlated modules were identified in fresh and five different dried samples. Additionally, a total of 23 hub VOCs can be recognized as the potential biomarkers for better distinguishing the fresh and five different dried Z. bungeanum.

Integrative analysis of non-targeted metabolome and transcriptome reveals the mechanism of volatile formation in pepper fruit.

Introduction: Aroma is a key inherent quality attributes of pepper fruit, yet the underlying mechanisms of aroma compound biosynthesis remain unclear. Methods: In this study, the volatile profile of the QH (cultivated Capsicum chinense) and WH (cultivated Capsicum annuum) pepper varieties were putatively identified during fruit development using gas chromatography-mass spectrometry (GC-MS). Results and discussion: The results identified 203 volatiles in pepper, and most of the esters, terpenes, aldehydes and alcohols were significantly down-regulated with fruit ripening. The comparison of volatile components between varieties revealed that aldehydes and alcohols were highly expressed in the WH fruit, while esters and terpenes with fruity or floral aroma were generally highly accumulated in the QH fruit, providing QH with a fruity odor. Transcriptome analysis demonstrated the close relationship between the synthesis of volatiles and the fatty acid and terpene metabolic pathways, and the high expression of the ADH, AAT and TPS genes was key in determining the accumulation of volatiles in pepper fruit. Furthermore, integrative metabolome and transcriptome analysis revealed that 208 differentially expressed genes were highly correlated with 114 volatiles, and the transcription factors of bHLH, MYB, ARF and IAA were identified as fundamental for the regulation of volatile synthesis in pepper fruit. Our results extend the understanding of the synthesis and accumulation of volatiles in pepper fruit.

Unraveling the terpene synthase family and characterization of BsTPS2 contributing to (S)-( +)-linalool biosynthesis in Boswellia.

Boswellia tree bark exudes oleo-gum resin in response to wounding, which is rich in terpene volatiles. But, the molecular and biochemical basis of wound-induced formation of resin volatiles remains poorly understood. Here, we combined RNA-sequencing (RNA-seq) and metabolite analysis to unravel the terpene synthase (TPS) family contributing to wound-induced biosynthesis of resin volatiles in B. serrata, an economically-important Boswellia species. The analysis of large-scale RNA-seq data of bark and leaf samples representing more than 600 million sequencing reads led to the identification of 32 TPSs, which were classified based on phylogenetic relationship into various TPSs families found in angiosperm species such as TPS-a, b, c, e/f, and g. Moreover, RNA-seq analysis of bark samples collected at 0-24h post-wounding shortlisted 14 BsTPSs that showed wound-induced transcriptional upregulation in bark, suggesting their important role in wound-induced biosynthesis of resin volatiles. Biochemical characterization of a bark preferentially-expressed and wound-inducible TPS (BsTPS2) in vitro and in planta assays revealed its involvement in resin terpene biosynthesis. Bacterially-expressed recombinant BsTPS2 catalyzed the conversion of GPP and FPP into (S)-( +)-linalool and (E)-(-)-nerolidol, respectively, in vitro assays. However, BsTPS2 expression in Nicotiana benthamiana found that BsTPS2 is a plastidial linalool synthase. In contrast, cytosolic expression of BsTPS2 did not form any product. Overall, the present work unraveled a suite of TPSs that potentially contributed to the biosynthesis of resin volatiles in Boswellia and biochemically characterized BsTPS2, which is involved in wound-induced biosynthesis of (S)-( +)-linalool, a monoterpene resin volatile with a known role in plant defense.

Hemoglobin and free iron influence the aroma of cooked beef by influencing the formation and release of volatiles

Cooked beef flavour is influenced by formation and release of odour-active volatiles. We hypothesised the aroma of cooked beef is affected by the concentration of heme proteins and free iron. To test our hypothesis, we spiked ground beef semitendinosus with different concentrations of hemoglobin or free iron. The patties were then grilled, and their volatile profiles were measured using gas chromatography – mass spectrometry and their sensory attributes were measured by a trained sensory panel. We found that spiking hemoglobin at 2 mg/g could suppress the release of linear aldehydes while increasing the formation of some Maillard-derived volatiles, which could potentially reduce the livery odour. The addition of free iron at 13.48 µg/g increased the livery and oxidised fat odour of cooked beef by increasing the formation of typical lipid-derived volatiles, such as 1-octen-3-ol, hexanal, and several akylfurans.

Study on the formation pathways of characteristic volatiles in preserved egg yolk caused by lipid species during pickling.

The formation of volatiles in high-fat foods is strongly influenced by the composition and structure of lipids. The relationship between key variable lipid species and characteristic volatiles were performed by lipidomics and flavoromics to resolve the pathways of volatiles in preserved egg yolk (PEY) during pickling. The results showed that the formation of nonanal and benzaldehyde at early stage possibly derived from oleic acid sited at Sn-1 in TG(18:1_18:2_20:4), Sn-2 in PE(22:6_18:1), and linoleic acid bonded at Sn-2 in TG(18:1_18:2_20:4), respectively. 1-octen-3-ol may be formed from linoleic acid located at Sn-2 in TG(18:1_18:2_20:4) and arachidonic acid sited at Sn-3 in TG(18:1_18:2_20:4). Indole was formed through TGs(16:0_16:1_20:1;16:1_18:1_22:1;23:0_18:1_18:1) at the later stage, and acetophenone through TGs(14:0_20:0_20:4;14:0_15:0_18:1; 16:0_16:0_22:6), PCs(24:0_18:1;O-18:1_18:2), PEs(P-18:1_20:4;P-18:1_22:6) and SPH(d18:0) during whole process of pickling. Our study provides a deep and precise insight for the formation pathways of characteristic volatiles in PEY through lipids degradation during pickling at the molecular level.