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1 ed this activity with putative mycobacterial cutinase.
2  bound efficiently and specifically to LFA-1/cutinase.
3 ceptor that presents the nonmammalian enzyme cutinase.
4  was more pronounced for the lipase than the cutinase.
5 imilar tertiary structure is Fusarium solani cutinase.
6 y Rhizopus oryzae lipase and Fusarium solani cutinase.
7 ut2/3 matched with that of the peptides from cutinase 1 and cutinase 2, respectively, isolated from F
8  assemblies can much more effectively retain cutinase 2 activity on a surface after co-incubation and
9 hese hydrophobins and their interaction with cutinase 2 is crucial for the development of novel antif
10 ith that of the peptides from cutinase 1 and cutinase 2, respectively, isolated from F. solani pisi g
11 esion and to direct the action of the enzyme cutinase 2, resulting in penetration of the plant host.
12 e, a fusion protein containing an N-terminal cutinase and a C-terminal SnapTag domain react with an e
13 ability, and structure of Aspergillus oryzae cutinase and compare it to the well-studied enzyme from
14                      Protein fusions between cutinase and five antibodies of three different types (s
15               Here we used the fungal enzyme cutinase and its suicide substrate p-nitrophenyl phospho
16 sity, using the covalent interaction between cutinase and its suicide substrate.
17 PETases compared to close relatives from the cutinase and lipase families have resulted in increasing
18                  Conversely, Fusarium solani Cutinase and lipases from Mycobacterium tuberculosis (Rv
19         The film was selectively degraded by cutinase and proteinase K to form a porous material.
20  carbohydrate esterase family 5 for putative cutinases and condensed it to 151 genes from known or pu
21 t encounter cutin; we demonstrate that known cutinases and MPLA cleave phospholipids in a PLA-type ma
22 cycling is gaining momentum, with engineered cutinases and PETases developed for the depolymerization
23  The covalent immobilization is specific for cutinase, and the glycol-terminated monolayer effectivel
24       These structural features of A. oryzae cutinase are proposed to result in an improved hydrolyti
25                                              Cutinases are esterases that release fatty acids from th
26                                              Cutinases are responsible for hydrolysis of the protecti
27                                              Cutinases are serine esterases whose primary substrate i
28 mon resonance (SPR) spectroscopy showed that cutinase binds irreversibly to a monolayer presenting th
29 tions, however, requires deeper knowledge of cutinases' biodiversity and structure-function relations
30 rganization with a catalytic triad common to cutinases, but which contains an additional four-helix d
31 ound to be essential for the inducibility of cutinase by hydroxy fatty acids.
32 dies suggest an alternative use for putative cutinases by the M. tuberculosis group that is likely re
33 e used to immobilize proteins of interest, a cutinase-calmodulin fusion protein was constructed and i
34 ionalized with a novel calmodulin construct, cutinase-calmodulin-cutinase (CutCaMCut), reversibly shi
35                                     Yet, the cutinase completely hydrolyzed all PBAT films, including
36 hey accept bulky and hydrophobic substrates, cutinases could be used in many applications, ranging fr
37 el calmodulin construct, cutinase-calmodulin-cutinase (CutCaMCut), reversibly shifts by 2-3 nm.
38                         The demonstration of cutinase-directed antibody immobilization with insert SA
39     We then selected nine phylogenic diverse cutinases for recombinant production and characterized t
40 hey undergo enzymatic hydrolysis by a fungal cutinase from Fusarium solani.
41 al dilute aqueous solutions or slurries, the cutinase from Humicola insolens can directly depolymeriz
42             Based on the in-silico search, a cutinase from Pseudomonas pseudoalcaligenes (PpCutA) and
43                                          Two cutinases from Fusarium solani and Cryptococcus sp. exhi
44 y expressing the enzyme Fusarium solani pisi cutinase (FsC) on the cell surface of Baker's yeast Sacc
45 (butylene adipate) films and Fusarium solani cutinase (FsC).
46 c sequence located at -159 base pairs of the cutinase gene in Fusarium solani f. sp. pisi (Nectria he
47                                 Expressing a cutinase gene in plants ectopically expressing MYB16 red
48 y binding selectively to palindrome 2 of the cutinase gene promoter.
49 n previously to induce the expression of the cutinase gene via a palindromic sequence located at -159
50            We cloned three highly homologous cutinase genes, cut1, cut2, and cut3, from Fusarium sola
51                            Each investigated cutinase had a unique activity fingerprint against the t
52  Asp175-His188-Ser120 of the serine esterase cutinase in the ground state.
53 y the low levels of constitutively expressed cutinase, induce high levels of cutinase that can help p
54 ed here provide insight into engineering new cutinase-inspired biocatalysts with tailor-made properti
55 uronidase gene fused to the promoters of the cutinases integrated into F. solani pisi genome indicate
56 polymerizing enzyme, leaf and branch compost cutinase (LCC).
57                                  We analyzed cutinase motifs in mycobacteria and found the motif very
58                  Action of this cell-surface cutinase on enzyme substrate self-assembled monolayers s
59 gh the heavy chain variable domain to either cutinase or SnapTag, with a linker terminated in an irre
60 ffectors by IC: phytotoxins, ROS, proteases, cutinases, plant cell wall-degrading enzymes and plant c
61  SV40 in yeast, it transactivated the native cutinase promoter fused to the chloramphenicol acetyl tr
62  of three microbial lipases: Fusarium solani cutinase, Rv0183, and LipY from Mycobacterium tuberculos
63 megamolecules are prepared by attaching four Cutinase-SnapTag fusion proteins (CS fusions) to a four-
64 ly expressed cutinase, induce high levels of cutinase that can help pathogenic fungi to penetrate int
65 m tuberculosis has maintained seven putative cutinases, though it should not encounter cutin; we demo
66 y is based on binding of the serine esterase cutinase to a self-assembled monolayer presenting a phos
67 cDNA clone encoding a polypeptide designated cutinase transcription factor 1alpha (CTF1alpha) with a
68  flavodoxin family (CheY, apoflavodoxin, and cutinase) using a simple nucleation and growth model tha
69                                              Cutinase was embedded in the extracellular domain of LFA
70                                              Cutinase was highly diastereoselective for the (Sp) conf
71           Further changes in the dynamics of cutinase were determined from quasiharmonic mode analysi
72         Nonlocal effects on the structure of cutinase were observed.
73 o a phylogenetic analysis, which showed that cutinases with available crystal structures were phyloge