Screening of a-amylase/trypsin inhibitor activity in wheat, spelt and einkorn by high-performance thin-layer chromatography

dc.contributor.authorMüller, Isabel
dc.contributor.authorSchmid, Bianca
dc.contributor.authorBosa, Loredana
dc.contributor.authorMorlock, Gertrud Elisabeth
dc.date.accessioned2025-11-18T11:00:04Z
dc.date.available2025-11-18T11:00:04Z
dc.date.issued2024
dc.description.abstractα-Amylase/trypsin inhibitor proteins (ATI) are discussed as possible triggers for non-celiac gluten sensitivity. The potential of high-performance thin-layer chromatography (HPTLC) was studied for the first time to analyse the inhibitory properties of ATIs from flour of wheat, spelt, and einkorn. Inhibition by each flour of the digestive enzymes trypsin or α-amylase was determined by the reduction of released metabolisation products in comparison to non-digested flour, and positive (acarbose) and negative (water) controls. Firstly, amylolysis was carried out in miniaturized form on the HPTLC surface (HPTLC-nanoGIT) after in-vial pre-incubation of the amylase with the inhibitors from flour. α-Amylase inhibition was evident via the reduction of released saccharides, as analysed by normal phase HPTLC. A strong influence of the flour matrix on the assay results (individual saccharides) was evident, caused by an increased amylolysis of further polysaccharides present, making HPTLC analysis more reliable than currently used spectrophotometric sum value assays. The detection and visualization of such matrix influence helps to understand the problems associated with spectrophotometric assays. Only maltotriose was identified as a reliable marker of the amylolysis. The highest α-amylase inhibition and thus the lowest saccharide response was detected for maltotriose in refined spelt, whereas the lowest α-amylase inhibition and thus the highest saccharide response was detected for maltotriose in refined wheat. A comparison of refined and whole grain flours showed no clear trend in the responses. Secondly, trypsin inhibition and proteolysis were performed in-vial, and any inhibition was evident via the reduction of released peptides, analysed by reversed-phase HPTLC. Based on the product pattern of the proteolysis, einkorn and whole wheat showed the highest trypsin inhibition, whereas refined wheat and refined spelt showed the lowest inhibition. Advantageously, HPTLC analysis provided important information on changes in individual saccharides or peptides, which was more reliable and sustainable than spectrophotometric in-vial assays (only sum value) or liquid column chromatography analysis (targeting only the ATI proteins).en
dc.description.sponsorshipDeutsche Forschungsgemeinschaft (DFG); ROR-ID:018mejw64
dc.identifier.urihttps://jlupub.ub.uni-giessen.de/handle/jlupub/21058
dc.identifier.urihttps://doi.org/10.22029/jlupub-20407
dc.language.isoen
dc.rightsNamensnennung 3.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/
dc.subject.ddcddc:640
dc.subject.ddcddc:360
dc.titleScreening of a-amylase/trypsin inhibitor activity in wheat, spelt and einkorn by high-performance thin-layer chromatography
dc.typearticle
local.affiliationFB 09 - Agrarwissenschaften, Ökotrophologie und Umweltmanagement
local.projectINST 162/536-1 FUGG and INST 162/471-1 FUGG
local.source.epage3006
local.source.journaltitleAnalytical methods
local.source.spage2997
local.source.urihttps://doi.org/10.1039/d4ay00402g
local.source.volume16

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