Formation kinetics of Maillard reaction intermediates from glycine–ribose system and improving Amadori rearrangement product through controlled thermal reaction and vacuum dehydration. (1st May 2020)
- Record Type:
- Journal Article
- Title:
- Formation kinetics of Maillard reaction intermediates from glycine–ribose system and improving Amadori rearrangement product through controlled thermal reaction and vacuum dehydration. (1st May 2020)
- Main Title:
- Formation kinetics of Maillard reaction intermediates from glycine–ribose system and improving Amadori rearrangement product through controlled thermal reaction and vacuum dehydration
- Authors:
- Zhan, Huan
Tang, Wei
Cui, Heping
Hayat, Khizar
Hussain, Shahzad
Tahir, Muhammad Usman
Zhang, Songlin
Zhang, Xiaoming
Ho, Chi-Tang - Abstract:
- Highlights: Amadori compound formation is the dominant reaction in vacuum dehydration. Controlled thermal reaction and vacuum dehydration improve Amadori compound yield. Reaction temperature and time are key factors to control byproduct content. Abstract: Amadori rearrangement product (ARP) is an ideal flavor precursor. The formation kinetics of ARP from glycine–ribose system, 3-deoxyribosone (3-DR) and 1-deoxyribosone (1-DR) were evaluated, and then controlled thermal reaction (CTR) coupled with vacuum dehydration was proposed to improve the ARP yield. As key factors controlling the formation of byproducts, CTR temperature and time were optimized as 100 °C, 60 min based on the formation kinetics of the ARP and deoxyribosones. Vacuum dehydration was further used to increase the ARP yield from 0.77% to 64.50%, which was improved by 82.8 times, while 3-DR and 1-DR yield increased only by 1.5 and 3.7 times, respectively. The formation of ARP was the dominant reaction during vacuum dehydration. Under optimal conditions, CTR coupled with vacuum dehydration was an effective method to control byproducts formation and improve the ARP yield simultaneously. This method may offer a potential application in flavor enhancement of light-color food.
- Is Part Of:
- Food chemistry. Volume 311(2020)
- Journal:
- Food chemistry
- Issue:
- Volume 311(2020)
- Issue Display:
- Volume 311, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 311
- Issue:
- 2020
- Issue Sort Value:
- 2020-0311-2020-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-05-01
- Subjects:
- d-Ribose (PubChem CID: 10975657) -- l-Glycine (PubChem CID: 750) -- N-(1-Deoxy-α-d-ribulos-1-yl)-glycine (PubChem CID: no items) -- 1-Deoxyribosone (PubChem CID: no items) -- 3-Deoxyribosone (PubChem CID: no items) -- Glyoxal (PubChem CID: 7860) -- Methylglyoxal (PubChem CID: 880) -- Diacetyl (PubChem CID: 650)
Formation kinetics -- Amadori rearrangement product -- 3-Deoxyribosone -- 1-Deoxyribosone -- Controlled thermal reaction -- Synergistic vacuum dehydration
Food -- Analysis -- Periodicals
Food -- Composition -- Periodicals
664 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03088146 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.foodchem.2019.125877 ↗
- Languages:
- English
- ISSNs:
- 0308-8146
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3977.284000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 12518.xml