Chemical synthesis of peptides within the insulin superfamily

2016 ◽  
Vol 22 (5) ◽  
pp. 260-270 ◽  
Author(s):  
Fa Liu ◽  
Alexander N. Zaykov ◽  
Jay J. Levy ◽  
Richard D. DiMarchi ◽  
John P. Mayer
Keyword(s):  
Chemical Synthesis ◽  
Insulin Superfamily

ChemInform Abstract: Chemical Synthesis of Peptides within the Insulin Superfamily

ChemInform ◽  
2016 ◽  
Vol 47 (29) ◽  
Author(s):  
Fa Liu ◽  
Alexander N. Zaykov ◽  
Jay J. Levy ◽  
Richard D. Di Marchi ◽  
John P. Mayer
Keyword(s):  
Chemical Synthesis ◽  
Insulin Superfamily

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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