AI Article Synopsis

  • The study explored how 11 types of oxygen-containing sulfur flavor molecules affect the stability of β-carotene when exposed to UVA light in an ethanol solution.
  • It was found that disulfides had a stronger impact on the breakdown of β-carotene compared to mono sulfides, with specific disulfides demonstrating first-order kinetics in degradation.
  • The resulting oxidation products of β-carotene were identified, and it was concluded that both the number of sulfur atoms and the presence of furan groups in these compounds significantly influence the photooxidation process.

Article Abstract

The influence of 11 kinds of oxygen-containing sulfur flavor molecules was examined on β-carotene stability under UVA irradiation in ethanol system. Both the effects of sulfides on dynamic degradation of β-carotene and the relation between structure and effect were investigated. The oxidation products of β-carotene accelerated by sulfides under UVA irradiation were also identified. The results indicated that the disulfides had more obvious accelerative effects on the photodegradation of β-carotene than mono sulfides. The degradation of β-carotene after methyl (2-methyl-3-furyl) disulfide (MMFDS), methyl furfuryl disulfide (MFDS) and bis(2-methyl-3-furyl) disulfide (BMFDS) exposure followed first-order kinetics. Furan-containing sulfides such as MMFDS and BMFDS showed more pronounced accelerative effects than their corresponding isomers. The oxidation products were identified as 13--β-carotene, 9,13-di--β-carotene and all--5,6-epoxy-β-carotene. These results suggest that both the sulfur atom numbers and the furan group in oxygen-containing sulfides play a critical role in the photooxidation of β-carotene.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6358934PMC
http://dx.doi.org/10.3390/molecules24020318DOI Listing

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