Article Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. The flavoprotein vanillyl alcohol oxidase (VAO) acts on a wide range of phenolic compounds and converts both creosol and vanillylamine to vanillin with high yield. Reaction of vanilmandelic acid and 4-hydroxybenzyl alcohol derivatives with L-ascorbic acid. Information. The VAO-mediated conversion of creosol proceeds via a two-step process in which the initially formed vanillyl alcohol is further oxidized … Find more information on the Altmetric Attention Score and how the score is calculated. It is a member of guaiacols and a member of benzyl alcohols. Corvini. Yaokang Wu, Xueqin Lv, Yanfeng Liu, Guocheng Du, Long Liu. Synth. Laboratory-evolved Vanillyl-alcohol Oxidase Produces Natural Vanillin. Due to increasing interest in natural vanillin, two enzymatic routes for the synthesis of vanillin were developed. 2001. Tetrahedron. http://pubs.acs.org/page/copyright/permissions.html. without permission from the American Chemical Society. Protein Engineering of Redox-Active Enzymes. Maria Inês F. Mota, Paula C. Rodrigues Pinto, José Miguel Loureiro, Alírio E. Rodrigues. Amanda Inés Mejía, Betty Lucy Lopez, Michael Hess. Ghahremani, M.R. Khoshayand, M.A. You have to login with your ACS ID befor you can login with your Mendeley account. Songwei Wang, Muhammad Bilal, Hongbo Hu, Wei Wang, Xuehong Zhang. Box 1, 2600 MA Delft, The Netherlands. Reaction of vanilmandelic acid and 4-hydroxybenzyl alcohol derivatives with L-ascorbic acid. Ultrasound-assisted oxidation of vanillyl alcohol 0.2 g (1.3 mmol) of vanillyl alcohol were dissolved in distilled water at 75 °C. 32:547-551. M. Hasan-Beikdashti, H. Forootanfar, M.S. the Altmetric Attention Score and how the score is calculated. culture medium. Enzyme-mediated oxidations for the chemist. Pravin Kumar, Shashwati Ghosh Sachan, Raju Poddar. Find more information on the Altmetric Attention Score and how the score is calculated. Aitor Hernández-Ortega, Patricia Ferreira, Angel T. Martínez. 31:3037-3040. not otherwise permitted to reproduce, republish, redistribute, or sell any Supporting Information 52:2741-2746. Recovery of Vanillin and Syringaldehyde from Lignin Oxidation: A Review of Separation and Purification Processes. You’ve supercharged your research process with ACS and Mendeley! Asai, H., Onozaki, H., and Imaseki, H. 1988. You’ve supercharged your research process with ACS and Mendeley! Phanerochaete chrysosporum
Jianfeng Jin, Hortense Mazon, Robert H. H. van den Heuvel, Dick B. Janssen, Marco W. Fraaije. Li, J.-T., Bian, Y.-J., Zang, H.-J., and Li, T.-S. 2002. Functional analysis of the vanillin pathway in a vdh-negative mutant strain of Pseudomonas fluorescens AN103. Article Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. Moreover, in the second step of the process, the conversion of vanillyl alcohol is inhibited by the competitive binding of creosol. You have to login with your ACS ID befor you can login with your Mendeley account. Meanwhile, 499.36 mg/L vanillyl alcohol was produced by COMT in vivo catalysis when fed with 1000 mg/L 3,4-dihydroxybenzyl alcohol. Mayuko Koreishi,, Demin Zhang,, Hiroyuki Imanaka,, Koreyoshi Imamura,, Shuji Adachi,, Ryuichi Matsuno, and. Get article recommendations from ACS based on references in your Mendeley library. Journal of Chemical Technology & Biotechnology. Peng Chen, Lei Yan, Zhengrong Wu, Suyue Li, Zhongtian Bai, Xiaojuan Yan, Ningbo Wang, Ning Liang, Hongyu Li. Mutational analysis of microbial hydroxycinnamoyl-CoA hydratase-lyase (HCHL) towards enhancement of binding affinity: A computational approach. Catalysis is limited by the formation of an abortive complex between enzyme-bound flavin and creosol. Journal of the Taiwan Institute of Chemical Engineers. The VAO-mediated conversion of creosol proceeds via a two-step process in which the initially formed vanillyl alcohol is further oxidized to vanillin. Citation: El-Sayed AM 2019. Production of biovanillin from wheat bran. https://doi.org/10.1021/acs.biochem.8b00920, https://doi.org/10.1016/bs.enz.2020.05.003, https://doi.org/10.1016/j.apcata.2019.117117, https://doi.org/10.1016/j.electacta.2018.01.111, https://doi.org/10.3390/molecules23010164, https://doi.org/10.1186/s13068-017-0720-5, https://doi.org/10.1007/s13213-017-1300-4, https://doi.org/10.1371/journal.pcbi.1005787, https://doi.org/10.1016/j.jmgm.2017.08.014, https://doi.org/10.1016/j.jct.2016.11.030, https://doi.org/10.1002/9781118354056.ch5, https://doi.org/10.1080/15422119.2015.1070178, https://doi.org/10.1007/s00253-015-6699-6, https://doi.org/10.1007/s13765-015-0078-y, https://doi.org/10.1007/s10562-014-1456-5, https://doi.org/10.1371/journal.pone.0105594, https://doi.org/10.1007/s13765-013-4277-0, https://doi.org/10.1007/s00253-013-4842-9, https://doi.org/10.1007/s12010-012-0066-1, https://doi.org/10.1007/s00253-012-4178-x, https://doi.org/10.1016/j.jtice.2012.03.005, https://doi.org/10.1007/s00253-011-3836-8, https://doi.org/10.1016/j.apcatb.2011.11.007, https://doi.org/10.1533/9780857095671.547, https://doi.org/10.1533/9780857095725.1.231, https://doi.org/10.1002/0471238961.sustmetz.a01.pub2, https://doi.org/10.1016/j.tibtech.2007.08.011, https://doi.org/10.1016/j.enzmictec.2007.04.003, https://doi.org/10.1007/s00284-006-0627-z, https://doi.org/10.1111/j.1742-4658.2007.05767.x, https://doi.org/10.1533/9781845692520.4.417, https://doi.org/10.1016/j.jbiotec.2006.03.024, https://doi.org/10.1016/j.enzmictec.2005.02.004, https://doi.org/10.1007/978-1-4419-8859-1_13, https://doi.org/10.1533/9781855738355.2.322, https://doi.org/10.1128/AEM.69.11.6569-6576.2003, https://doi.org/10.1016/S0031-9422(03)00149-3, https://doi.org/10.1007/s10019-003-0239-1, https://doi.org/10.1007/978-3-540-49339-6_22, https://doi.org/10.1007/978-3-540-49339-6_9. Gudrun Gygli, Maria Fátima Lucas, Victor Guallar, Willem J. H. van Berkel, . Journal of the Korean Society for Applied Biological Chemistry. The flavoprotein vanillyl alcohol oxidase (VAO) acts on a wide range of phenolic compounds and converts both creosol and vanillylamine to vanillin with high yield. Pastore. Catharine A. Adams, Kolea Zimmerman, Kristi Fenstermacher, Mitchell G. Thompson, Will Skyrud, Scott Behie, Anne Pringle, . Convenient and clean synthesis of imines from primary benzylamines. Current awareness in flavour and fragrance. Fermentation of hot pepper juice by Bacillus licheniformis to reduce pungency. Safiarian, A. Ameri, M.H. A microbial transformation using Bacillus subtilis B7-S to produce natural vanillin from ferulic acid. Fanny Lambert, Joseph Zucca, Frédérique Ness, Michel Aigle. Journal of Agricultural and Food Chemistry. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. HR167. Development of a genetically programed vanillin-sensing bacterium for high-throughput screening of lignin-degrading enzyme libraries. Fengli Wu, Peng Cao, Guotian Song, Wujiu Chen, Qinhong Wang. Vanillyl alcohol is a phenolic alcohol and is used as a flavoring agent in foods and beverages. Recovery and reuse of trimmings and pulps from fruit and vegetable processing. Faramarzi. NOTES FOR THIS EXPERIMENT: Zeolites as Shape-Selective Catalysts: Highly Selective Synthesis of Vanillin from Reimer–Tiemann Reaction of Guaiacol and Chloroform. Your Mendeley pairing has expired. Exploring the Promiscuity of Phenol Hydroxylase from Pseudomonas stutzeri OX1 for the Biosynthesis of Phenolic Compounds. An Enzymatic Platform for the Synthesis of Isoprenoid Precursors. Files available from the ACS website may be downloaded for personal use only. The American Chemical Society holds a copyright ownership interest in any copyrightable Supporting Additionally, the present study demonstrates the application of enzyme promiscuity of COMT in the design of an artificial pathway for the production of high-value methylated aromatic compounds. Junzhi Wang, Cheng Zheng, Yang Cao, Zhuotao Tan, Dong Liu, Zhuopei Cheng, Hanjie Ying, Huanqing Niu. Vanillin Synthesis from 4-Hydroxybenzaldehyde. These metrics are regularly updated to reflect usage leading up to the last few days. Production of ferulic acid and coniferyl alcohol by conversion of eugenol using a recombinant strain of
Yufen Chen, Peiling Wu, Liang-Yu Ko, Tzu-Yu Kao, Lijun Liu, Yang Zhang. Frank Hollmann, Isabel W. C. E. Arends, Katja Buehler, Anett Schallmey, Bruno Bühler. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Direct Aromatic Nitration System for Synthesis of Nitrotryptophans in Escherichia coli. Microbial transformation of propenylbenzenes for natural flavour production. The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online.