ライフサイエンスコーパス: L-asparagine

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1 cells in vitro is prevented upon addition of L-asparagine.

2 e correct positioning of l-glutamine but not l-asparagine.

3 rmination in response to either D-alanine or L-asparagine also caused faster spore germination with t

4 bly by reducing the affinity of the site for L-asparagine, although the enzyme retains cooperativity.

5 te dependence curve with an [S](0.5) of 1 mM L-asparagine and a Hill coefficient (n(H)) of 2.6.

6 ion containing an equimolar concentration of L-asparagine and D-glucose showed a significant inhibiti

7 s an enzyme that catalyzes the hydrolysis of L-asparagine and isoaspartyl-peptides.

8 pores germinated similarly with a mixture of l-asparagine and KCl (AK), KCl alone, or a 1:1 chelate o

9 -cpe isolates in that (i) while a mixture of L-asparagine and KCl was a good germinant for spores of

10 tive in germination with a rich medium, KCl, L-asparagine, and a 1:1 chelate of Ca(2+) and dipicolini

11 type spores with KCl, did not germinate with L-asparagine, and germinated poorly compared to wild-typ

12 Gold nanoparticles synthesized using L-Asparagine as reducing and stabilization agent were em

13 Initially, N-CDs were prepared from L-asparagine by pyrolysis and characterized by different

14 ation of the GerB receptor with D-alanine or L-asparagine can trigger spore germination independently

15 nation with either L-alanine or a mixture of L-asparagine, D-glucose, D-fructose, and potassium ions.

16 y property to allow the required therapeutic l-asparagine depletion.

17 ndings indicate that pathogens similarly use L-asparagine deprivation to limit T cell responses.

18 ermination of gerB* spores with D-alanine or L-asparagine did not require participation of the produc

19 Here, we show that poly-L-asparagine forms polar zippers similar to those of pol

20 325 can displace dansyl sarcosine and dansyl-L-asparagine from HSA with inhibition constants (K(i)) o

21 ase catalyzes the ATP-dependent formation of L-asparagine from L-aspartate and L-glutamine, via a bet

22 iggered spore germination cooperatively with l-asparagine, fructose, and K+ and either L-alanine or L

23 s in the germination rates with D-alanine or L-asparagine in spores overexpressing gerB* were well be

24 ethyl ester, L-glutamic acid dimethyl ester, L-asparagine, L-aspartic acid beta-methyl ester, and L-a

25 Several carbon sources (L-Asparagine, L-Aspartic Acid, L- Glutamic Acid, m- Eryt

26 eved by a group of amino acids that includes l-asparagine, l-glutamine, l-threonine, l-arginine, l-gl

27 yl)-L-glutamine and N-1-(1-deoxy-D-mannityl)-L-asparagine served as substrates for MOP oxidoreductase

28 r an asparagine or a glutamine increases the l-asparagine specificity but only when combined with the

29 t into the molecular basis for the increased l-asparagine specificity.

30 evaluation of immunosensors fabricated using L-Asparagine stabilized gold nanoparticles and citrate s

31 zed gold nanoparticles and (3) directly onto L-Asparagine stabilized gold nanoparticles modified elec

32 Binding of L-asparagine to an allosteric site was observed in the c

33 ginase II, which catalyzes the hydrolysis of L-asparagine to aspartic acid and ammonia.

34 ses, enzymes that catalyze the hydrolysis of L-asparagine to aspartic acid, have been used for over 3

35 P-cpe isolates, KCl and, to a lesser extent, L-asparagine triggered spore germination in C-cpe isolat

36 = N(4)-[7-(trifluoromethyl)-9H-fluoren-2-yl]-L-asparagine (WAY-212922) (IC(50) = 157 +/- 11 nM) = 3-{

37 5 nM) > N(4)-(2'-methyl-1,1'-biphenyl-4-yl)-L-asparagine (WAY-213394) (IC(50) = 145 +/- 22 nM) = N(4

38 N(4)-[4-(2-bromo-4,5-difluorophenoxy)phenyl]-L-asparagine (WAY-213613) (IC(50) = 85 +/- 5 nM) > N(4)-

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