Literature DB >> 17319686

Enzymatic dehydrogenative polymerization of urushiols in fresh exudates from the lacquer tree, Rhus vernicifera DC.

Sayoko Harigaya1, Takayuki Honda, Lu Rong, Tetsuo Miyakoshi, Chen-Loung Chen.   

Abstract

Fresh exudates from the lacquer tree, Rhus vernicifera DC, were extracted with acetone and the solution was chromatographed to isolate monomer, dimer, trimer, and oligomer fractions of urushiols. Constituents of the monomeric and dimeric fractions were then identified by two-dimensional (2D) 1H-13C heteronuclear multiple quantum coherence (HMQC) and heteronuclear multiple bond coherence (HMBC) NMR spectroscopic techniques. The results showed that the monomeric fraction contained 3-[8'Z,11'E,13'Z-pentadecatrienyl]catechol (1), 3-[8'Z,11'Z,14'-pentadecatrienyl]catechol (2), and 3-pentadecanyl]catechol (3), which was verified by HPLC analysis. The dimeric fraction contained 8'-(3' ',4' '-dihydroxy-5' '-alkenyl)phenyl-3-[9'E,11'E,13'Z-pentadecatrienyl]catechol (4), 14'-(3' ',4' '-dihydroxy-5' '-alkenyl)phenyl-3-[8'Z,10'E,12'E-pentadecatrienyl]catechol (5), 2-hydroxyl-3- or -6-alkenylphenyl ethyl ether (6), 14'-(3' ',4' '-dihydroxy-2' '-alkenyl)phenyl-3-[8'Z,10'E,12'E-pentadeca-trienyl]catechol (7), 15'-(2' '-hydroxy-3' '- or -6' '-alkenyl)phenyloxy-3-[8'Z,11'Z,13'E)-pentadecatrienyl]catechol (8), 14'-(2' ',3' '-dihydroxy-4' '-alkenyl)phenyl-3-[8'Z,10'E,12'E-pentadecantrienyl]catechol (9), 1,1',2,2'-tetrahydroxy-6,6'-dialkenyl-4,3'-biphenyl (10), 1,1',2,2'-tetrahydroxy-6,6'-dialkenyl-4,4'-biphenyl (11), 1,1',2,2'-tetrahydroxy-6,6'-dialkenyl-5,4'-biphenyl (12), and 1,2,1'-trihydroxy-6,6'-dialkenyldibenzofuran (13) as constituents. In addition, dimeric ethers and peroxides, such as compounds 14 and 15, were produced by autoxidation of monomeric urushiols in atmospheric air. The possible reaction mechanisms for the dehydrogenative polymerization of urushiols by Rhus laccase present in the fresh raw exudates under the atmospheric oxygen are discussed on the basis of structures identified. This is of primary importance because the use of the urushi exudates as coating materials does not involve organic solvents and is an environmentally friendly process.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17319686     DOI: 10.1021/jf063161g

Source DB:  PubMed          Journal:  J Agric Food Chem        ISSN: 0021-8561            Impact factor:   5.279


  4 in total

1.  Polymerized urushiol of the commercially available rhus product in Korea.

Authors:  Seung Hyun Cheong; You Won Choi; Byung Sun Min; Hae Young Choi
Journal:  Ann Dermatol       Date:  2010-02-28       Impact factor: 1.444

2.  The chromosome-level genome for Toxicodendron vernicifluum provides crucial insights into Anacardiaceae evolution and urushiol biosynthesis.

Authors:  Guoqing Bai; Chen Chen; Chenxi Zhao; Tao Zhou; Dan Li; Tianhua Zhou; Weimin Li; Yuan Lu; Xiaofeng Cong; Yun Jia; Sifeng Li
Journal:  iScience       Date:  2022-06-02

3.  In vitro antibacterial and morphological effects of the urushiol component of the sap of the Korean lacquer tree (Rhus vernicifera Stokes) on Helicobacter pylori.

Authors:  Ki Tae Suk; Hyun Soo Kim; Moon Young Kim; Jae Woo Kim; Young Uh; In Ho Jang; Soo Ki Kim; Eung Ho Choi; Myong Jo Kim; Jung Soo Joo; Soon Koo Baik
Journal:  J Korean Med Sci       Date:  2010-02-17       Impact factor: 2.153

4.  Improved Measurements of the Physical Properties of Oriental Lacquers Using Atomic Force Microscopy and a Nanoindenter.

Authors:  Hye Hyun Yu; Jung-Ah Lim; Kang-Bong Lee; Yeonhee Lee
Journal:  Polymers (Basel)       Date:  2021-04-26       Impact factor: 4.329

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.