Stereoselective production of dimethyl-substituted carbapenams via engineered carbapenem biosynthesis enzymes
Stereoselective biocatalysis by crotonase superfamily enzymes is exemplified by use of engineered 5-carboxymethylproline synthases (CMPSs) for preparation of functionalized 5-carboxymethylproline (5-CMP) derivatives methylated at two positions (i.e. C2/C6, C3/C6 and C5/C6), including products with a...
Κύριοι συγγραφείς: | Hamed, R, Henry, L, Claridge, T, Schofield, C |
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Μορφή: | Journal article |
Έκδοση: |
American Chemical Society
2016
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Παρόμοια τεκμήρια
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Biosynthesis of carbapenem antibiotics: new carbapenam substrates for carbapenem synthase (CarC).
ανά: Sleeman, M, κ.ά.
Έκδοση: (2004) -
Crotonase catalysis enables flexible production of functionalized prolines and carbapenams.
ανά: Hamed, R, κ.ά.
Έκδοση: (2012) -
Synthesis of regio- and stereoselectively deuterium-labelled derivatives of L-glutamate semialdehyde for studies on carbapenem biosynthesis.
ανά: Ducho, C, κ.ά.
Έκδοση: (2009) -
Stereoselective preparation of lipidated carboxymethyl-proline/pipecolic acid derivatives via coupling of engineered crotonases with an alkylmalonyl-CoA synthetase.
ανά: Hamed, R, κ.ά.
Έκδοση: (2013) -
The use of carbonyl group anisotropy effect in determination of the relative configuration of carbapenams
ανά: Olga Staszewska-Krajewska, κ.ά.
Έκδοση: (2014-01-01)