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1 f the Sh1 gene that encodes maize (Zea mays) sucrose synthase.
2 he fruit can be accomplished by invertase or sucrose synthase.
3 chimeric gene construction, in which a corn sucrose synthase-1 gene (Sh) promoter was used to direct
4 insight into the roles of this motif in rice sucrose synthase 3 (RSuS3), the two conserved glutamate
5 development there is a transient increase in sucrose synthase activity and starch which is correlated
6 ol of a fruit-specific promoter we show that sucrose synthase activity can be reduced by up to 99% in
8 s and cleavage, as well as the regulation of sucrose synthase and its interactions with cellular targ
9 avage during expansion was sustained by both sucrose synthase and neutral invertase, associated with
10 ty in rs/rs roots whereas neutral invertase, sucrose synthase and sucrose phosphate synthase levels w
11 s increased accumulations of transcripts for sucrose synthase and vacuolar invertase were both observ
12 s the changing intracellular localization of sucrose synthase as a molecular switch between survival
15 , electron microscopic immunolocalization of sucrose synthase in cotton fibers, and phylogenetic rela
16 in vitro, and is required for expression of sucrose synthase in potato tubers and excised leaves.
17 result calls into question the importance of sucrose synthase in regulating sink strength in tomato f
22 ose synthase, possible regulation by Ca2+ of sucrose synthase localization, electron microscopic immu
23 eolus vulgaris roots, a Rhizobium-responsive sucrose synthase of soybean and a cell wall acid inverta
24 predominantly located in phloem tissues for sucrose synthase or the endodermis and phloem for solubl
25 included on phosphorylation of cotton fiber sucrose synthase, possible regulation by Ca2+ of sucrose
26 by a phloem-specific promoter (from the rice sucrose synthase RSs1 gene) and by a constitutive promot
33 e 170 (S170) of the maize (Zea mays L.) SUS1 sucrose synthase (SUS) protein as a possible, second pho
35 is tightly coexpressed with two isoforms of sucrose synthase (SUS5 and SUS6) known to be confined to
36 d cell-specific, yet functionally redundant, sucrose synthase (SuSy) genes, Sh1 and Sus1, which encod
37 eriments were conducted to determine whether sucrose synthase (SuSy) was phosphorylated in the elonga
38 lower expression of SbSUS4, a gene encoding sucrose synthase that generates UDP-glucose from sucrose
39 pose that UGT1 may transfer UDP-glucose from sucrose synthase to the callose synthase and thus help f
40 phofructokinase during cell division and for sucrose synthase, UDP-glucopyrophosphorylase, and phosph
41 ASE (VvPDC), ALCOHOL DEHYDROGENASE (VvADH2), SUCROSE SYNTHASE (VvSUSY), non-symbiotic HEMOGLOBIN (Vvn
43 s and fermentation genes and a gene encoding sucrose synthase were more strongly induced in the less
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