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1 r role for just one enzyme, granular binding starch synthase.
2 , result from the primary deficiency in this starch synthase.
3 ls of ADPglucose (ADPglc), the substrate for starch synthases.
4 distinct from the C-terminal region of other starch synthases.
6 sis mutant lacking the glucosyl-transferase, STARCH SYNTHASE 4 (SS4) is impaired in its ability to in
10 plast-localized biosynthetic enzymes, namely starch synthases, ADP-glucose pyrophosphorylase, and sta
11 cept for two starch synthases, granule bound starch synthase and starch synthase II, which increased
13 if common to the ADP-glucose-binding site of starch synthases and bacterial glycogen synthases, funct
14 ertheless, each type of BE together with the starch synthases and debranching enyzmes were able to cr
17 y genes encoding isoforms of AGPase, soluble starch synthase, and other starch branching enzymes were
18 enzymes like ADP-glucose pyrophosphorylase, starch synthases, and debranching enzymes, leading to va
19 ipts encoding starch synthase, granule-bound starch synthase, chitinase, lectin, and a type-2 metallo
22 manner, whereas genes encoding granule-bound starch synthase, debranching enzymes, pullulanase, and s
23 those for ADP glucose pyrophosphorylase and starch synthase, do not produce detectable decay interme
26 pectrometry-based proteomics, granular-bound starch synthase (GBSS) is the major granular protein in
27 The rice Waxy gene encodes a granule-bound starch synthase (GBSS) necessary for the synthesis of am
29 psis (Arabidopsis thaliana) in GRANULE-BOUND STARCH SYNTHASE (GBSS), encoding the enzyme responsible
30 ew insights into the action of GRANULE BOUND STARCH SYNTHASE (GBSS), the major glucosyltransferase th
31 rophosphorylase, ADPGlc PPase; granule bound starch synthase, GBSS; starch synthases, SSI, SSII, SSII
32 taining either wx (lacking the granule-bound starch synthase GBSSI) or ae wx (lacking both SBEIIb and
34 e relative abundance of transcripts encoding starch synthase, granule-bound starch synthase, chitinas
35 ly little in amount over 24 h except for two starch synthases, granule bound starch synthase and star
36 thaliana mutants lacking the SS4 isoform of starch synthase have strongly reduced numbers of starch
38 y distinct from genes encoding granule-bound starch synthase I (Waxy protein) and starch synthase I.
39 the waxy protein plus significant levels of starch synthase I and starch branching enzyme II (BEII)
40 sses of 76 and 85 kD have been identified as starch synthase I and starch branching enzyme IIb, respe
41 that the C-terminal region of granule-bound starch synthase I confers most of the specific propertie
44 indicated increased levels of granule-bound starch synthase I in the soluble nonzein protein fractio
46 waxy protein, more than 85% total endosperm starch synthase I protein, and more than 45% of BEII pro
47 SNP in the promoter region of Granule Bound Starch Synthase I was identified along with seven other
48 nscription factor MYB103, a putative soluble starch synthase I, and a homeodomain-leucine zipper tran
49 32 kD or above, including the waxy protein, starch synthase I, and starch-branching enzyme IIb, rema
50 or two functional waxy genes (granule-bound starch synthase I, or GBSSI) produces starch with interm
53 two enzymes involved in starch biosynthesis, starch synthase II (SSII) and starch branching enzyme II
54 between the zSSIIa and zSSIIb clones and the starch synthase II clones of potato and pea ranges betwe
55 I from potato has been compared with that of starch synthase II from potato following expression of b
56 synthases, granule bound starch synthase and starch synthase II, which increased appreciably during t
57 ted the interdependence of the maize enzymes starch synthase IIa (SSIIa), SSIII, starch branching enz
61 maize (Zea mays) genes dull1 (du1), encoding starch synthase III (SSIII), and isa2, encoding a noncat
62 ed in an Arabidopsis Atss3 mutant that lacks starch synthase III and has increased leaf starch conten
64 munocapture using antibodies to DU1, a maize starch synthase III family member, and direct interactio
69 indicated an interaction between SBDCP1 and starch synthase IIIa (SSIIIa), which was down-regulated
72 enzymes alkaline pyrophosphatase and soluble starch synthase, less than 2% of the cytosolic marker en
74 The increase in RNA encoding granule-bound starch synthase may reflect the extensive destruction of
76 leiotropic effects of sbe1a genes on SBEIIa, starch synthase, or starch-debranching enzyme isoforms w
81 PPase; granule bound starch synthase, GBSS; starch synthases, SSI, SSII, SSIII; and starch branching
82 s study identified the complement of soluble starch synthases (SSs) present in developing maize (Zea
83 is thaliana) mutants lacking combinations of starch synthases (SSs) SS1, SS2, and SS3 (to vary chain
84 of the starch biosynthetic system, including starch synthases (SSs), starch branching enzymes (BEs),
86 ers and distribution and the accumulation of starch synthase substrates and products were investigate
87 identity of the zSSIIa and zSSIIb clones as starch synthases was confirmed by expression of enzyme a
88 t D-genome Gss locus, encoding granule-bound starch synthase, were sequenced in a total 564 lines of
89 ate of ADP-Glc pyrophosphorylase and soluble starch synthase, which catalyze the first committed and