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1 the structure of all three domains only with isoamylase.
2  substrates enabled its classification as an isoamylase.
3               The starch debranching enzymes isoamylase 1 and 2 (ISA1 and ISA2) are known to exist in
4  studies identified two debranching enzymes, isoamylase 3 (ISA3) and limit dextrinase (LDA), involved
5 ch-degrading enzymes including beta-amylase, isoamylase 3, and alpha-amylase was also reduced in the
6  gene are known to cause deficiencies of SU1 isoamylase and a pullulanase-type DBE.
7                  This is readily degraded by isoamylase and other enzymes so it does not accumulate a
8 hey tag OsHXK6 (rice hexokinase), ISA2 (rice isoamylase) and a tandem array of sugar transporters.
9  other DBEs identified motifs common to both isoamylase- and pullulanase-type enzymes, as well as cla
10  This study identified and purified specific isoamylase- and pullulanase-type starch-debranching enzy
11                  In C. reinhardtii, the STA7 isoamylase gene is important for the accumulation of cry
12  gene complementation were used to link this isoamylase gene to previously characterized nontagged st
13                                   A putative isoamylase gene was mined from megagenomic database.
14 ne that shows high homology to the family of isoamylase genes found in several photosynthetic organis
15 oplasts in the mutant lines, suggesting that isoamylase has an indirect rather than a direct role in
16 e for simultaneous starch gelatinization and isoamylase hydrolysis.
17 etabolism catalyzed by starch phosphorylase, isoamylase is essential to debranch alpha-1,6-glycosidic
18              This enzyme was the most stable isoamylase reported with a half lifetime of 200 min at 9
19                             The loss of this isoamylase resulted in a 90% reduction in the accumulati
20            However, there is no thermostable isoamylase stable enough for simultaneous starch gelatin
21 n ss2ss3 per se is not limiting but that the isoamylase suppresses glucan accumulation.
22 tt-based air-breathing biobattery powered by isoamylase-treated starch exhibited nearly doubled power
23 as identified as a debranching enzyme of the isoamylase type.
24 type activity was identified as ZPU1 and the isoamylase-type activity as SU1.
25 ee su1- alleles severely reduce or eliminate isoamylase-type DBE activity, although su1-st kernels ac
26 mays) gene sugary1 (su1), which codes for an isoamylase-type DBE, condition distinct kernel phenotype
27 have not been described, although defects in isoamylase-type DBE, known in many plant species, indica
28  DBE partially compensates for the defect in isoamylase-type DBE, suggesting a function during starch
29    Furthermore, in a background deficient in isoamylase-type DBE, zpu1-204 conditions a significant a
30                             Pullulanase- and isoamylase-type DBEs were purified from extracts of deve
31  of phytoglycogen accumulation when the only isoamylase-type debranching activity present is ISA1 hom
32 for normal glucan accumulation when the only isoamylase-type debranching enzyme activity present is I
33                     These data indicate that isoamylase-type debranching enzyme and SSIII work in a c
34                                              Isoamylase-type starch debranching enzymes (ISA) play im
35                                    Conserved isoamylase-type starch debranching enzymes (ISAs), inclu
36                                 Functions of isoamylase-type starch-debranching enzyme (ISA) proteins
37 coding a noncatalytic subunit of heteromeric isoamylase-type starch-debranching enzyme (ISA1/ISA2 het
38 l plants examined is altered by mutations of isoamylase-type starch-debranching enzymes (DBE), althou

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