Chemical Synthesis of the 20 kDa Heme Protein Nitrophorin 4 by α-Ketoacid-Hydroxylamine (KAHA) Ligation

2015 ◽  
Vol 54 (44) ◽  
pp. 12996-13001 ◽  
Author(s):  
Chunmao He ◽  
Sameer S. Kulkarni ◽  
Frédéric Thuaud ◽  
Jeffrey W. Bode
Keyword(s):  
Chemical Synthesis ◽  
Heme Protein ◽  
Nitrophorin 4

Chemical Synthesis of the 20 kDa Heme Protein Nitrophorin 4 by α-Ketoacid-Hydroxylamine (KAHA) Ligation

2015 ◽  
Vol 127 (44) ◽  
pp. 13188-13193 ◽  
Author(s):  
Chunmao He ◽  
Sameer S. Kulkarni ◽  
Frédéric Thuaud ◽  
Jeffrey W. Bode
Keyword(s):  
Chemical Synthesis ◽  
Heme Protein ◽  
Nitrophorin 4

scholarly journals The crystal structure of nitrophorin 4 at 1.5 å resolution: transport of nitric oxide by a lipocalin-based heme protein

Structure ◽  
1998 ◽  
Vol 6 (10) ◽  
pp. 1315-1327 ◽  
Author(s):  
John F Andersen ◽  
Andrzej Weichsel ◽  
Celia A Balfour ◽  
Donald E Champagne ◽  
William R Montfort
Keyword(s):  
Crystal Structure ◽  
Nitric Oxide ◽  
Heme Protein ◽  
Nitrophorin 4

Chemical synthesis of proteinoids: Part 1

1964 ◽  
Author(s):  
Sidney W. Fox ◽  
Kaoru Harada ◽  
Gottfried Krampitz ◽  
Tadao Hayakawa ◽  
Charles Ray Windsor
Keyword(s):  
Chemical Synthesis

Chemical Synthesis of Peptides

2012 ◽  
Vol 2 (2) ◽  
pp. 147-149
Author(s):  
Tanaji Dnyanadev Padalkar ◽  
Keyword(s):  
Chemical Synthesis

Microbe Engineering of Guaia-6,10(14)-diene as a Building Block for the Semisynthetic Production of Plant-Derived (−)-Englerin A

2019 ◽  
Author(s):  
Thomas Siemon ◽  
Zhangqian Wang ◽  
Guangkai Bian ◽  
Tobias Seitz ◽  
Ziling Ye ◽  
...  
Keyword(s):  
Escherichia Coli ◽  
Saccharomyces Cerevisiae ◽  
Synthetic Biology ◽  
Chemical Synthesis ◽  
Building Block ◽  
Transient Receptor Potential ◽  
Receptor Potential ◽  
Economical Method ◽  
Englerin A ◽  
Transient Receptor

Herein, we report the semisynthetic production of the potent transient receptor potential canonical (TRPC) channel agonist (−)-englerin A (EA), using guaia-6,10(14)-diene as the starting material. Guaia-6,10(14)-diene was systematically engineered in Escherichia coli and Saccharomyces cerevisiae using the CRISPR/Cas9 system and produced with high titers. This provided us the opportunity to execute a concise chemical synthesis of EA and the two related guaianes (−)-oxyphyllol and (+)-orientalol E. The potentially scalable approach combines the advantages of synthetic biology and chemical synthesis and provides an efficient and economical method for producing EA as well as its analogs.

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