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Inside Back Cover: A Tandem Enzymatic sp2‐C‐Methylation Process: Coupling in Situ S‐Adenosyl‐l‐Methionine Formation with Methyl Transfer (ChemBioChem 11/2017)
The inside back cover picture shows a one‐pot tandem reaction involving in situ enzymatic synthesis of S‐adenosylmethionine by using SalL, followed by C−C bond formation by using the C‐methyltransferase NovO. This system is compatible with both methionine and methionine analogues as the alkyl donor....
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Published in: | Chembiochem : a European journal of chemical biology 2017-06, Vol.18 (11), p.1050-1050 |
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container_end_page | 1050 |
container_issue | 11 |
container_start_page | 1050 |
container_title | Chembiochem : a European journal of chemical biology |
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creator | Sadler, Joanna C. Humphreys, Luke D. Snajdrova, Radka Burley, Glenn A. |
description | The inside back cover picture shows a one‐pot tandem reaction involving in situ enzymatic synthesis of S‐adenosylmethionine by using SalL, followed by C−C bond formation by using the C‐methyltransferase NovO. This system is compatible with both methionine and methionine analogues as the alkyl donor. More information can be found in the communication by L. D. Humphreys, G. A. Burley et al. on page 992 in Issue 11, 2017 (DOI: 10.1002/cbic.201700115). |
doi_str_mv | 10.1002/cbic.201700244 |
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subjects | Adenosylmethionine alkylation biocatalysis Bonding Cascade chemical reactions Chemical synthesis Compatibility Coupling Enzymatic synthesis Methionine Methylation Methyltransferase multi-enzyme reaction S-Adenosylmethionine |
title | Inside Back Cover: A Tandem Enzymatic sp2‐C‐Methylation Process: Coupling in Situ S‐Adenosyl‐l‐Methionine Formation with Methyl Transfer (ChemBioChem 11/2017) |
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