Proanthocyanidin Block Arrays (PACBAR) for Comprehensive Capture and Delineation of Proanthocyanidin Structures

被引:13
作者
Jing, Shuxi [1 ,2 ]
Zeller, Wayne E. [3 ]
Ferreira, Daneel [4 ,5 ]
Zhou, Bin [6 ]
Nam, Joo-Won [7 ]
Bedran-Russo, Ana [8 ]
Chen, Shao-Nong [1 ,2 ]
Pauli, Guido F. [1 ,2 ]
机构
[1] Univ Illinois, Coll Pharm, Pharmacognosy Inst, Chicago, IL 60612 USA
[2] Univ Illinois, Coll Pharm, Dept Pharmaceut Sci, Chicago, IL 60612 USA
[3] ARS, US Dairy Forage Res Ctr, USDA, Madison, WI USA
[4] Univ Mississippi, Natl Ctr Nat Prod Res, University, MS 38677 USA
[5] Univ Mississippi, Dept Biomol Sci, Div Pharmacognosy, Sch Pharm, University, MS 38677 USA
[6] Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R China
[7] Yeungnam Univ, Coll Pharm, Gyongsan 38541, Gyeongsangbuk D, South Korea
[8] Marquette Univ, Sch Dent, Dept Gen Dent Sci, Milwaukee, WI 53233 USA
基金
美国国家卫生研究院;
关键词
proanthocyanidins; polyphenols; nomenclature; structure-activity relationships; OLIGOMERIC PROANTHOCYANIDINS; CONDENSED TANNINS; PROCYANIDINS; INHIBITOR; PHENOLS;
D O I
10.1021/acs.jafc.0c05392
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Proanthocyanidins (PACs) are near-ubiquitous and chemically complex metabolites, prototypical of higher plants. Their roles in food/feed/nutrition and ethnomedicine are widely recognized but poorly understood. With the analysis of evidence that underlies this challenge, this perspective identifies shortcomings in capturing and delineating PAC structures as key factors. While several groups have forwarded new representations, a consensus method that captures PAC structures concisely and offers high integrity for electronic storage is required to reduce confusion in this expansive field. The PAC block arrays (PACBAR) system fills this gap by providing precise and human- and machine-readable structural descriptors that capture PAC metabolomic structural diversity. PACBAR enables communication of PAC structures for the development of precise structure-activity relationships and will assist in advancing PAC research to the next level.
引用
收藏
页码:13541 / 13549
页数:9
相关论文
共 40 条
[31]   Highly polymerized procyanidins in brown soybean seed coat with a high radical-scavenging activity [J].
Takahata, Y ;
Ohnishi-Kameyama, M ;
Furuta, S ;
Takahashi, M ;
Suda, I .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2001, 49 (12) :5843-5847
[32]   Phenolic group on A-ring is key for dracoflavan B as a selective noncompetitive inhibitor of α-amylase [J].
Toh, Zhi Siang ;
Wang, Hongyu ;
Yip, Yew Mun ;
Lu, Yuyun ;
Lim, Benedict Jeffrey Ang ;
Zhang, Daiwei ;
Huang, Dejian .
BIOORGANIC & MEDICINAL CHEMISTRY, 2015, 23 (24) :7641-7649
[33]   Analysis of commercial proanthocyanidins. Part 1: The chemical composition of quebracho (Schinopsis lorentzii and Schinopsis balansae) heartwood extract [J].
Venter, Pieter B. ;
Sisa, Mirek ;
van der Merwe, Marthinus J. ;
Bonnet, Susan L. ;
van der Westhuizen, Jan H. .
PHYTOCHEMISTRY, 2012, 73 :95-105
[34]   Mimicking the Hierarchical Functions of Dentin Collagen Cross-Links with Plant Derived Phenols and Phenolic Acids [J].
Vidal, Cristina M. P. ;
Leme, Ariene A. ;
Aguiar, Thaiane R. ;
Phansalkar, Rasika ;
Nam, Joo-Won ;
Bisson, Jonathan ;
McAlpine, James B. ;
Chen, Shao-Nong ;
Pauli, Guido F. ;
Bedran-Russo, Ana .
LANGMUIR, 2014, 30 (49) :14887-14893
[35]   Role of anthocyanidin reductase, encoded by BANYULS in plant flavonoid biosynthesis [J].
Xie, DY ;
Sharma, SB ;
Paiva, NL ;
Ferreira, D ;
Dixon, RA .
SCIENCE, 2003, 299 (5605) :396-399
[36]   Unified approach to catechin hetero-oligomers: first total synthesis of trimer EZ-EG-CA isolated from Ziziphus jujuba [J].
Yano, Takahisa ;
Ohmori, Ken ;
Takahashi, Haruko ;
Kusumi, Takenori ;
Suzuki, Keisuke .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2012, 10 (38) :7685-7688
[37]   Activity, Purification, and Analysis of Condensed Tannins: Current State of Affairs and Future Endeavors [J].
Zeller, Wayne E. .
CROP SCIENCE, 2019, 59 (03) :886-904
[38]   The US Dairy Forage Research Center (USDFRC) Condensed Tannin NMR Database [J].
Zeller, Wayne E. ;
Schatz, Paul F. .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2017, 65 (25) :5104-5106
[39]   Rare A-Type, Spiro-Type, and Highly Oligomeric Proanthocyanidins from Pinus massoniana [J].
Zhou, Bin ;
Alania, Yvette ;
Reis, Mariana C. ;
McAlpine, James B. ;
Bedran-Russo, Ana K. ;
Pauli, Guido F. ;
Chen, Shao-Nong .
ORGANIC LETTERS, 2020, 22 (14) :5304-5308
[40]   Tri- and Tetrameric Proanthocyanidins with Dentin Bioactivities from Pinus massoniana [J].
Zhou, Bin ;
Alania, Yvette ;
Reis, Mariana ;
Phansalkar, Rasika S. ;
Nam, Joo-Won ;
McAlpine, James B. ;
Chen, Shao-Nong ;
Bedran-Russo, Ana K. ;
Pauli, Guido F. .
JOURNAL OF ORGANIC CHEMISTRY, 2020, 85 (13) :8462-8479