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1 ne in the sequence of reactions catalyzed by phytoene desaturase.
3 ts contained an insertion in a gene encoding phytoene desaturase, an enzyme of carotenoid biosynthesi
4 stewartii, and the two carotene desaturases phytoene desaturase and carotene zeta-carotene desaturas
5 ded a vector, BMVCP5, that better maintained phytoene desaturase and heat shock protein70-1 (HSP70-1)
6 block the carotenoid pathway at the level of phytoene desaturase and induce the accumulation of phyto
7 arrying geranylgeranyl diphosphate synthase, phytoene desaturase and the bacterial carotene desaturas
8 to target an endogenous transcript encoding PHYTOENE DESATURASE and used to analyze the role of miR1
9 ownstream enzymes, required two desaturases (phytoene desaturase and zeta-carotene desaturase [ZDS])
11 olutionarily preserved activity of bacterial phytoene desaturases and plant carotenoid isomerases.
13 hange the product of Rhodobacter sphaeroides phytoene desaturase (crtI gene product), a neurosporene-
15 identified: phytoene synthase (crtB/CT1386), phytoene desaturase (crtP/CT0807), zeta-carotene desatur
16 ts are rescued by inhibitors or mutations of phytoene desaturase, demonstrating that phytofluene and/
17 share significant similarity and a putative phytoene desaturase domain with a recently described pla
18 chocystis sp. PCC 6803 the genes that encode phytoene desaturase (encoded by crtP (pds)) and zeta-car
20 ions of this FoMV vector system, four genes, phytoene desaturase (functions in carotenoid biosynthesi
21 genes of Synechocystis sp. PCC 6803 with the phytoene desaturase gene (crtI) of Rhodobacter capsulatu
25 ith a control construct or one that silences phytoene desaturase had no effect on resistance or susce
27 ude that the differences in the mechanism of phytoene desaturase inhibition play an important role in
29 ces is effective at silencing the endogenous phytoene desaturase (PapsPDS) gene in Papaver somniferum
30 mate-1-semialdehyde aminotransferase (GSAT), phytoene desaturase (PDS) and light-harvesting polypepti
32 at express a fragment of the nuclear-encoded Phytoene desaturase (PDS) gene capable of catalyzing pos
34 gineered with magnesium chelatase (ChlH) and phytoene desaturase (PDS) gene sequences from Nicotiana
35 cylic acid differed statistically in normal, phytoene desaturase (PDS) gene silent and diseased (infe
36 ent protein (gfp) transgene or an endogenous phytoene desaturase (pds) gene, generated a stronger and
37 ences from the RNA leader of the Arabidopsis phytoene desaturase (pds) gene, when inserted into the 3
39 ne desaturase gene (zds) or both the zds and phytoene desaturase (pds) genes of Synechocystis sp. PCC
41 nalyzed 20 progeny plants of Cas12a-mediated phytoene desaturase (PDS) mutagenized regenerants, as we
42 nd expressing the VIGS constructs to silence Phytoene desaturase (PDS) or a ribosomal protein-encodin
43 tenoid biosynthetic pathway, a cDNA encoding phytoene desaturase (PDS) was isolated and characterized
44 h we successfully silenced the expression of phytoene desaturase (PDS), a 20S proteasome subunit (PB7
45 to zeta-carotene, carried out by the enzyme phytoene desaturase (PDS), is one of the earliest steps
46 pressing transgenic sorghum lines, targeting Phytoene desaturase (PDS), Magnesium-chelatase subunit I
47 by phytoene synthase (PSY), two desaturases (phytoene desaturase [PDS] and zeta-carotene desaturase [
49 hereas in the dark mainly zeta-carotene, the phytoene desaturase product, accumulates, illumination l
50 f green fluorescent protein and silencing of phytoene desaturase shows that marker gene-assisted sile
52 ,15,9'-tri-cis-zeta-carotene, the product of phytoene desaturase, to form 9,9'-di-cis-zeta-carotene,
53 -PCR of intact RNA showed that the amount of phytoene desaturase transcripts increased after HHP trea
54 s, and the biosynthetic activity upstream of phytoene desaturase was similar in Newhall and Cara Cara
55 l carotenoid gene (crtI) encoding the enzyme phytoene desaturase, which converts phytoene into lycope