ライフサイエンスコーパス: plant type

1 ting to carbon assimilation, which differ by plant type.

2 el differences in acclimation capacity among plant types.

3 Rd acclimation was similar across plant types.

4 e of this study was to determine whether the plant type 1 peroxisomal targeting signal (PTS1) utilize

5 ucoseen reductase (E3), is an NADH dependent plant type [2Fe-2S] containing flavoenzyme.

6 The enzyme exhibits a strong preference for plant type [2Fe-2S] ferredoxins; however, flavodoxin can

7 rotein with one Rieske [2Fe-2S] cluster, one plant-type [2Fe-2S] cluster, and one flavin mononucleoti

8 vided by essential interactions with reduced plant-type [2Fe-2S] ferredoxin (Fd).

9 A reductase, which contains FMN and a plant-type [2Fe-2S] ferredoxin domain, transfers electro

10 act that E(max) was roughly conserved across plant types and scales with the product of xylem saturat

11 y composition surpassed the variation due to plant type, and microbial communities under each crop di

12 energy into biomass is 4.6-6%, depending on plant type, and the best year-long efficiencies realized

13 adients of precipitation, edaphic qualities, plant types, and/or land use change.

14 eu is critical for the catalytic function of plant-type APS reductases by promoting the interdomain i

15 elucidated the first N-terminal nucleophile plant-type asparaginase structure in the covalent interm

16 e maturation of hedgehog signaling proteins, plant-type asparaginases, and pyruvoyl enzymes.

17 Similar to nonmammalian plant-type asparaginases, hASRGL1 is shown to be an Ntn

18 tivity consistent with enzymes designated as plant-type asparaginases, which had thus far been found

19 a subunit fold similar to that observed in "plant"-type beta class carbonic anhydrases.

20 Here we report on the first known plant-type (beta-class) carbonic anhydrase in the archae

21 t carbon exchange is common across different plant types, but that acclimation to warmer temperatures

22 nd shrubs and competitive interactions among plant types, confirmed by structural equation analysis.

23 evolution from bacterial-type SRP to higher plant-type cpSRP system.

24 The stereoselectivity of the plant-type desaturation pathway expressed in E. coli is

25 e also important determinants in controlling plant-type distributions.

26 study provides experimental evidence that a plant-type FA beta-oxidation involving H2 O2 -producing

27 Chlamydomonas reinhardtii genome encodes six plant type [Fe2S2] ferredoxins, products of PETF, FDX2-F

28 by the [Fe-Fe]-hydrogenase HYDA1, which uses plant type ferredoxin PETF/FDX1 (PETF) as an electron do

29 t contains flavin mononucleotide (FMN) and a plant-type ferredoxin [2Fe-2S] center.

30 s heterodimeric; SDH2N and SDH2C contain the plant-type ferredoxin domain in the N-terminal half and

31 center is not distinguishable from those in plant-type ferredoxins.

32 < 0.001) and was relatively conserved among plant types (for a given plant size), while increasing a

33 recently discovered in Arabidopsis thaliana plant-type histidinol phosphate phosphatase (HPP) shares

34 Together with a few other plant type I OMTs, we demonstrated that our Gibbs' reage

35 vities in vitro and in vivo, and some of the plant type II MCPs exhibit Ca(2+) dependence for their e

36 CPA and U-73122 are inhibitors of plant type IIA calcium pumps and phospholipase C, respec

37 oward tailoring the biosynthetic activity of plant type III PKS.

38 emble the most recent common ancestor of the plant type III PKSs.

39 The plant type III polyketide synthases (PKSs), which produc

40 erence between the susceptible and resistant plant types is determined at an earlier stage in saponin

41 A plant-type lycopene beta-cyclase gene crtL was identifie

42 Two varieties, japonica (tropical; new plant type [NPT]) and indica (IR72) were compared.

43 ted with either high-phosphate iron mineral (plant-type) or low-phosphate iron mineral (animal-type)

44 ises from a tight interaction between 107-kD plant-type PEPC and 118-kD bacterial-type (BTPC) subunit

45 r and that they both originate from the same plant-type PEPC gene.

46 complex stress-related (LHCSR)-dependent and plant-type S subunit of Photosystem II (PSBS)-dependent

47 Both plant types showed toxicity tolerance, but metal accumul

48 modern carbon isotope compositions in all C3 plant types shows a monotonic increase in delta(13)C wit

49 ic acid, regardless of fullerene presence or plant type, significantly decreased the p,p'-DDE uptake.

50 chemical-induced CAC, oral administration of plant-type sphingolipids called sphingadienes increased

51 ding can be used more efficiently to develop plant types that can combine all or most of the benefici

52 Unlike the plant-type VDE that is located in the thylakoid lumen, t

53 Two transgenic plant types were used; in the first, functional antibody

54 different photosynthetic processes varied by plant type, with C3 species tending to preferentially ac