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1  was prepared and resolved by porcine kidney acylase.
2  applicable to the characterization of other acylases.
3 nas aeruginosa, as a template to generate an acylase able to effectively hydrolyze C8-HSL, the major
4                          It also exhibits an acylase activity, capable of deacylating N-acetyl-Met-Le
5  the N-acylated substrate by an L-amino acid acylase and its subsequent oxidation by an FAD-dependent
6 to describe the roles and regulation of de-S-acylases and how extracellular signals drive dynamic (de
7  study of the substrate specificity of other acylases and peptidases.
8 stances, including vitamin B(12), penicillin acylase, and amylases.
9 trates the effectiveness of quorum-quenching acylases as potential novel antimicrobial drugs.
10                        Herein we describe an acylase (CmCDA from Cyclobacterium marinum) that catalyz
11        The crystal structure of penicillin G acylase from Escherichia coli has been determined to a r
12 precursor mutant (Thr263Gly) of penicillin G acylase from Escherichia coli, which reveals that the sp
13                  Among these, lactonases and acylases have been particularly studied.
14 cetyl-L-alanine at 298.35K by porcine kidney acylase I (EC 3.5.1.14) was monitored by the heat releas
15 mma-glutamyl-cysteine ligase (gamma-GCL) and acylase I activities.
16 ine, and N-acetyl-L-phenylalanine by porcine acylase I in 0.1M phosphate buffer, which is inhibited b
17         This protein was identified as the N-acylase IA (or N(alpha)-acyl-l-amino acid amidohydrolase
18 openicillanic acid catalyzed by Penicillin G acylase in miniaturized stirred batch reactors or contin
19                                 Penicillin G acylase is a periplasmic protein, cytoplasmically expres
20 lts reveal that ligand binding in penicillin acylase is facilitated by certain amino acid residues th
21                                    Since the acylase is thermally stable and the pH of the phosphate
22 e report that SIRT2, a potent lysine defatty-acylase, is upregulated by the transcription factor CREB
23                        The enzyme penicillin acylase (penicillin amidohydrolase EC 3.5.1.11) catalyse
24 ng group that can be removed by penicillin G acylase (PGA).
25  inactivation mutant of tem25 encoding a (de)acylase, structurally elucidated, and then shown to be d
26                          Tafazzin is a trans-acylase that acylates immature monolysocardiolipin to ma
27 tructural protoxin, and lktC encodes a trans-acylase that adds fatty acid chains to internal lysine r
28             For penicillin and cephalosporin acylases, this discrepancy between structure and functio
29 ant has been coupled with an enantiospecific acylase to give a preparative scale dynamic kinetic reso
30                   We engineered penicillin G acylases to distinguish among free amino moieties of ins
31 neglecting acetate product inhibition of the acylase, values for k(cat) were up to a factor of 2.3 la
32 spired by the extraordinary selectivities of acylases, we envisioned the use of lipophilic oligopepti