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1 phaseolin, indicating an interaction between phaseolin and polyphenols.
2 bacco seeds utilizing the seed specific bean phaseolin and soybean beta-conglycinin promoters.
3  primarily associated with nutrient storage (phaseolin) and carbohydrate metabolism (lectins) were si
4 nd that the levels of phosphorylation of the phaseolin changed remarkably in the seed transition from
5 henotype in plants transformed with the bean phaseolin/CP 3-5 was variable.
6 ved for another assembly defective mutant of phaseolin, delta360, which remains monomeric and does no
7                                 Based on the phaseolin digestibility in vitro and phaseolin-polypheno
8 oduction of transcripts encoding the protein phaseolin during seed embryogenesis but is silent in veg
9 ity of beans by decreasing the hydrolysis of phaseolin, especially in the darker ones.
10 in isolate fractions, and B1, B2, and B3 for phaseolin fractions) were assayed for antioxidant and me
11                 MARs found flanking the beta-phaseolin gene (phas) were tested for insulating activit
12             In beans, expression of the beta-phaseolin gene (phas), encoding the major seed storage p
13 e results suggest that ABA induction of beta-phaseolin gene expression is modulated by developmental
14                                              Phaseolin genes are induced by unidentified factors at t
15  Thus, fractions coming from the isolate and phaseolin had similar activities except for iron chelati
16                                              Phaseolin has not been detected in the endosperm, which
17 orts the hypothesis that mobilization of the phaseolin in germinating seeds occurs through the degrad
18 e synthesis, accumulation and degradation of phaseolin in the common bean seed are not yet sufficient
19 difference in the electrophoretic pattern of phaseolin, indicating an interaction between phaseolin a
20                          The polyphenols and phaseolin interaction in common bean varieties was studi
21 s except for iron chelation, suggesting that phaseolin is the major contributor to the antioxidant an
22                                              Phaseolin is the major seed storage protein of common be
23 bolic variations suggest that phosphorylated phaseolin isoforms have functional significance.
24  the presence and dynamics of phosphorylated phaseolin isoforms.
25 our results indicate that post-translational phaseolin modifications through phosphorylations need to
26 ing of maturation, as phytohemagglutinin and phaseolin mRNAs were induced.
27                         The promoter for the phaseolin (phas) bean seed protein gene adopts an inacti
28                Extensive studies of the beta-phaseolin (phas) gene in transgenic tobacco have shown t
29 sence of transcriptional expression from the phaseolin (phas) gene promoter in leaf tissue and that t
30                  Here, we use studies on the phaseolin (phas) gene that encodes a seed protein to sho
31                                     The beta-phaseolin (phas) gene, which encodes one of the major se
32                         The promoter for the Phaseolin (phas) gene, which encodes the major seed stor
33                                          The phaseolin (phas) promoter drives copious production of t
34                       Transcription from the phaseolin (phas) promoter requires two major events: chr
35 oters of phytohemagglutinin (DLEC2) and beta-phaseolin (PHS beta) genes.
36 us to identify differentially phosphorylated phaseolin polypeptides in dormant and germinating seeds
37  on the phaseolin digestibility in vitro and phaseolin-polyphenol complexation obtained by SDS-PAGE o
38 e show that in tobacco, expression of a beta-phaseolin promoter-GUS (PHSbeta-uidA) mRNA and the corre
39 ng for phytohemagglutinin L-subunit and beta-phaseolin, respectively, is coordinately induced in bean
40 ed Fc fragment under the control of the beta-PHASEOLIN seed-specific promoter.
41 and Trp-rich sequence to the C-terminus of a phaseolin variant lacking its vacuolar sorting signal, w
42 d tryptophan of the trimeric storage protein phaseolin, we fused a Met- and Trp-rich sequence to the
43                     Bean protein isolate and phaseolin were hydrolysed using pepsin and pancreatin, a
44 nits of type alpha and beta that compose the phaseolin were identified by matrix-assisted laser desor

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