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1 erimental SAXS profile of the homotetramer D-xylose isomerase.
2 ation states of amino acids in crystals of D-xylose isomerase.
3 in the case of Streptomyces olivochromogenes xylose isomerase.
4 s that rhamnose isomerase is most similar to xylose isomerase.
5 ls of rhamnose isomerase are very similar to xylose isomerase.
6 s enzyme from all other previously described xylose isomerases.
7 el alternate transcripts and included both a xylose isomerase 1 domain and a GTPase domain.
8 xylAB operon, comprising genes that encode D-xylose isomerase and D-xylulose kinase, lies a 1,101-bp
9 rupting two genes (xylA and EcxylB) encoding xylose isomerase and xyloluse kinase.
10 tabolism enabled through the introduction of xylose isomerase and xylulokinase.
11                            We cloned a new D-xylose isomerase derived from microorganisms in the gut
12                                              Xylose isomerase (E.C. 5.3.1.5) catalyzes the interconve
13 owed that the enzyme had 98% homology with a xylose isomerase from a closely related bacterium, Therm
14 rried shared mutations: amplification of the xylose isomerase gene and inactivation of ISU1, a gene e
15 c library to identify multiple copies of the xylose isomerase gene as a genomic change contributing t
16  amino acid sequence with sequences of other xylose isomerases in the database showed that the enzyme
17 ft mechanism, which is generally favored for xylose isomerase, is also feasible for rhamnose isomeras
18 rray of hydrophobic residues, not present in xylose isomerase, is likely to be responsible for the re
19 es through heterologous expression of fungal xylose isomerase or modification of cofactor requirement
20 S12 strain was obtained by introducing the D-xylose isomerase pathway from Escherichia coli, followed
21 ring in a strain engineered to express the D-xylose isomerase pathway, we demonstrate that mutations
22                                   An unusual xylose isomerase produced by Thermoanaerobacterium strai
23 ificantly from the T. saccharolyticum B6A-RI xylose isomerase suggested that one or more of the obser
24  be a dehydrogenase, actually belongs to the xylose isomerase superfamily.
25                                       Unlike xylose isomerase, this loop does not extend across a sub
26                                   Like other xylose isomerases, this enzyme required Mn2+, Co2+, or M
27 nt between AsbF and other enzymes within the xylose isomerase TIM-barrel family.
28                        The gene encoding the xylose isomerase was cloned and expressed in Escherichia
29                                            D-Xylose isomerase (XI) and triosephosphate isomerase (TIM
30 -xylose through expression of heterologous D-xylose isomerase (XI).
31 e location of hydrogen atoms in the enzyme d-xylose isomerase (XI).
32 egies were implemented to explore new active xylose isomerases (XIs) for Saccharomyces cerevisiae.
33                The N + Q content of class II xylose isomerases (XIs) from mesophiles, moderate thermo
34 s were threefold higher than in strain B for xylose isomerase (xylA) and twofold higher for xylulokin
35                           The genes encoding xylose isomerase (xylA) and xylulose kinase (xylB) from