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1 to be enriched in starch debranching enzyme (pullulanase).
2 ng enzyme besides the neopullulanase and the pullulanase.
3 rgistic effect was found under conditions of pullulanase (1 U/ml/5h) and IR (220 (o)C/3 min) treatmen
4 ches were subjected to enzymatic hydrolysis (pullulanase, 40 U/g per 10h), autoclaved (121 degrees C/
5 es encoding the extracellular SpeB protease, pullulanase A (PulA), and two extracellular nucleases (S
6 gradation; pulA encodes a cell wall anchored pullulanase and amyA encodes a freely secreted putative
7 reated sorghum grains were modified by using pullulanase and infrared (IR) irradiation to decrease st
8              Previously, a neopullulanase, a pullulanase, and an alpha-glucosidase from B. thetaiotao
9 -bound starch synthase, debranching enzymes, pullulanase, and starch phosphorylases were largely down
10                                              Pullulanase- and isoamylase-type DBEs were purified from
11 f how thioredoxin h enhances the activity of pullulanase because it was found that the inhibitor had
12 prepared from elephant foot yam starch using pullulanase enzyme.
13 ristics with PulJ, a pseudopilin involved in pullulanase export in Klebsiella oxytoca.
14  and two enzymes modification (alpha-amylase/pullulanase) falls under the former classification and t
15 ing) and two enzymes modification (a-amylase/pullulanase) falls under the former classification and t
16 enhanced by debranching cassava starch using pullulanase followed by high pressure or cyclic high-pre
17 mutant, with a disruption in susA and in the pullulanase gene, pulI, was also able to grow on pullula
18                                              Pullulanase is a well-known starch-debranching enzyme.
19             However, the production level of pullulanase is yet low in both wide-type strains and het
20 e activity of the starch debranching enzyme, pullulanase (limit dextrinase), the enzyme that specific
21 beta-amylase, starch phosphorylase, maltase, pullulanase or D-enzyme could be detected in crude extra
22  are deficient in a different type of DBE, a pullulanase (or R enzyme).
23 isorder propensities of Bacillus naganoensis pullulanase (PUL) using the bioinformatics tool, Disorde
24 olysaccharide (LPS) O-polysaccharide and the pullulanase (PulA) type 2 secretion system (T2SS) are re
25                        The gene encoding the pullulanase, pulI, was not located in this region in the
26 ) and the outer membrane protein PulD of the pullulanase secretion system failed to identify a compar
27                                       In the pullulanase-secretion system, PulS, an outer membrane-as
28                                          The pullulanase-type activity was identified as ZPU1 and the
29                 Thus, hydrolytic activity of pullulanase-type DBE contributes to starch catabolism.
30 r maltooligosaccharides, indicating that the pullulanase-type DBE functions in glucan hydrolysis duri
31             We describe a null mutation of a pullulanase-type DBE gene, a Mutator insertion in maize
32                    Mutations that affect the pullulanase-type DBE have not been described, although d
33                                   Therefore, pullulanase-type DBE partially compensates for the defec
34  kernels, indicating that it is the affected pullulanase-type DBE.
35 h a rice (Oryza sativa L.) cDNA coding for a pullulanase-type DBE.
36 o cause deficiencies of SU1 isoamylase and a pullulanase-type DBE.
37 tified motifs common to both isoamylase- and pullulanase-type enzymes, as well as class-specific sequ
38 tified and purified specific isoamylase- and pullulanase-type starch-debranching enzymes (DBEs) prese
39                    The debranching effect of pullulanase was stabilized by the IR radiation amplifyin