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Highly Enantioselective sec ‐Alkyl Sulfatase Activity of the Marine Planctomycete Rhodopirellula baltica Shows Retention of Configuration
Author(s) -
Wallner Sabine R.,
Bauer Marga,
Würdemann Chris,
Wecker Patricia,
Glöckner Frank O.,
Faber Kurt
Publication year - 2005
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.200501955
Subject(s) - enantioselective synthesis , baltica , alkyl , cleavage (geology) , hydrolysis , chemistry , stereochemistry , catalysis , geology , organic chemistry , paleontology , ordovician , fracture (geology)
Hydrolytic enzymes : The marine planctomycete Rhodopirellula baltica DSM 10527 displays high stereo‐ and enantioselective alkyl sulfatase activity towards (±)‐ sec ‐alkyl sulfates with retention of configuration through cleavage of their SO bond (see scheme; pathway B), whereas inversion of configuration is observed upon cleavage of the CO bond (pathway A).