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1 hytoene synthase and PSY2, a putative second phytoene synthase.
2 s and Myxococcus xanthus crtB genes encoding phytoene synthase.
3 s of maize was sequenced and found to encode phytoene synthase.
4 genome editing we validated the function of PHYTOENE SYNTHASE 1 (PSY1) gene in affecting millet grai
6 anisms, acting predominantly at the level of phytoene synthase-1 (PSY1), and feed-forward mechanisms
7 fruit phenotype of the r,r mutant and Psy-1 (phytoene synthase-1) antisense tomatoes is due to a muta
8 ruit color accumulation (bifunctional 15-cis-phytoene synthase, 9-cis-epoxycarotenoid dioxygenase, be
9 hosphate (IPP) was used as the substrate for phytoene synthase a reduction (e.g. r,r mutant, 5-fold)
10 s, as well as with the enhanced abundance of phytoene synthase, a key enzyme in the carotenoid biosyn
12 rotenoid content, on two maize genes, the Y1 phytoene synthase and PSY2, a putative second phytoene s
13 d the expression of HMG2, PSY1 (the gene for phytoene synthase), and lycopene accumulation before the
16 the following six enzymes to be identified: phytoene synthase (crtB/CT1386), phytoene desaturase (cr
18 ymes geranylgeranyl diphosphate synthase and phytoene synthase, from the soil bacterium Erwinia stewa
21 Transformation with a wild-type copy of the phytoene synthase gene was able to complement the lts1-2
24 Our findings underscore the diverse roles of phytoene synthase in shaping horticultural traits, and r
27 e acting upon diketopiperazine substrates, a phytoene synthase-like prenyltransferase as the catalyst
29 matoes is due to a mutated or down-regulated phytoene synthase protein, respectively, resulting in th
32 ined, or sequence or abundance of mRNAs from phytoene synthase (PSY) and chromoplast-specific lycopen
35 orophyll biosynthesis pathway in addition to phytoene synthase (PSY) in carotenoid biosynthesis pathw
39 ltered splicing and C-terminal truncation of phytoene synthase (PSY), a key enzyme in carotenoid bios
41 limiting enzyme for carotenoid biosynthesis, phytoene synthase (PSY), as compared with white-rooted c
42 hypothesized that the daffodil gene encoding phytoene synthase (psy), one of the two genes used to de
43 ent, we began to characterize genes encoding phytoene synthase (PSY), since this nuclear-encoded enzy
44 control the expression of the gene encoding PHYTOENE SYNTHASE (PSY), the first and main rate-determi
45 he plastid-localized GGPS isoform GGPS11 and phytoene synthase (PSY), the first enzyme of the caroten
46 eract with GBFs to activate transcription of phytoene synthase (PSY), the gene encoding a rate-limiti
48 ceed through a poly-cis pathway catalyzed by phytoene synthase (PSY), two desaturases (phytoene desat
52 isrupting the activity of the fruit-specific phytoene synthase (PSY1), the first committed step in th
55 te synthase rather than squalene synthase or phytoene synthase, which catalyze c1'-2-3 cyclopropanati