ライフサイエンスコーパス: optimum pH

1 e the same or at least similar values of the optimum pH.

2 eference (1.2-fold) for linoleic acid at its optimum pH.

3 The optimum pH 4.2-4.6 for autocatalysis was different than

4 mol P1 cross-linked min-1mg-1 enzyme, at the optimum pH 5.5.

5 s-Kell has an acidic pH optimum (pH 6.0 to 6.5).

6 kDa), temperature maximum (80 degrees C), pH optimum (pH 6.3), and isoelectric point (pH 4.5) that we

7 nce of the endonuclease activity of Glu-274 (optimum pH = 6.5) is distinct from that of the wild-type

8 o related proteases, in its more alkaline pH optimum (pH 7-8), its relative resistance to calcium che

9 ix hydrolases, the enzyme has an alkaline pH optimum (pH 8) and requires a divalent cation for activi

10 + with double-stranded substrates, a high pH optimum (pH 8-9) and inhibition by monovalent cations.

11 The hydrolysis reaction is pH-dependent (optimum pH = 9.5) and is slower, by a factor of 10(-5),

12 enzyme in hydrolysis of the covalent adduct (optimum pH = 9.5).

13 Optimum pH, affinity to MgATP and constants for the inhi

14 The correlation between the optimum pH and base/acid ratio is significant if only bu

15 It was demonstrated that the optimum pH and isoelectric point could be quite differen

16 Under optimum pH and Mg(2+) conditions this ribozyme cleaves a

17 pecificity, requirement for lipid cofactors, optimum pH and Mg2+, and other intrinsic properties.

18 The optimum pH and solvents for extraction by SPE and potent

19 The optimum pH and temperature for enzyme activity were pH 1

20 The optimum pH and temperature for the proteolytic activity

21 The optimum pH and temperature for xylanase activity were 4.

22 zymes produced were very different regarding optimum pH and they showed stability at 50 degrees C.

23 s and disfavors the bases tends to have high optimum pH and vice versa.

24 duced a functional enzyme that had a neutral optimum pH and was dramatically inhibited by low concent

25 18)O isotope effects at pH 5.7 (close to the optimum pH) and at pH 7.7 (away from the optimum pH) are

26 tase with respect to its Mg(2+) requirement, optimum pH, and sensitivity to cations, amino acids, and

27 the optimum pH) and at pH 7.7 (away from the optimum pH) are respectively 1.016 +/- 0.003 and 1.014 +

28 Furthermore, the Q224E mutant showed an optimum pH at 6.2, which is 1.5 pH units lower than that

29 dent of the ionic strength, and exhibited an optimum pH between 7.0 and 7.5.

30 The optimum pH for both reactions was 7.0.

31 The optimum pH for cleavage is 5.0 (half-life, approximately

32 The optimum pH for ethanol oxidation was between 9.4 and 10.

33 tein cleavage products are determined at the optimum pH for generating tryptic fragments, directly fr

34 Optimum pH for maximum sorption was obtained at 6.0.

35 We demonstrate that the optimum pH for methanogenesis by this organism is lower

36 The optimum pH for the binding of melamine was found to be 4

37 nts, thus suggesting that there should be an optimum pH for the catalytic turnover.

38 donor (citrate-phosphate as pH buffer), the optimum pH for the function of POD-A was 4.6, and the op

39 Optimum pH for the ligation reaction of the human telome

40 The optimum pH for the removal of Cu(2+) ions by CA-BS was a

41 The optimum pH for this reaction is 5.0.

42 Immobilised enzyme showed a shift in the optimum pH; however, optimum temperature remained unaffe

43 to Ru ratios are needed (100:1) and that the optimum pH is near 5.0.

44 The RNase H has a basic optimum pH, is active only in the presence of reducing a

45 enzyme could also hydrolyse lactose, with an optimum pH of 4.0 at 40 degrees C.

46 M13 substrate, the helicase activity had an optimum pH of 7 to 7.5, an optimum temperature of 45 deg

47 A Km of 45 microM and an optimum pH of 7-8 was observed with bradykinin as the su

48 At the optimum pH of 7.0, the oxidation of LD occurs at a poten

49 n optimum temperature of 75 degrees C and an optimum pH of 7.5.

50 enzyme requires Mg(2+) for activity, has an optimum pH of 7.6, and is strongly stimulated by deterge

51 of Syrian hamster Sc237 PrP(Sc) displays an optimum pH of approximately 7, whereas amplification of

52 eins, found experimentally to have different optimum pH of maximal stability, were studied to reveal

53 The optimum pH of the enzyme was 2.8 and it hydrolysed o-nit

54 catalytic efficiency, but showed an altered optimum pH preference for maximum activity.

55 ACS isozymes function as dimers and have an optimum pH, ranging between 7.3 and 8.2.

56 It was shown that the optimum pH results from two factors - amino acid composi

57 Each enzyme has been characterized as to pH optimum, pH stability, isoelectrofocusing and susceptibi

58 The pI of the protein, and optimum pH/temperature of enzyme activity were 4.4, 5 an

59 re was a tendency for proteins having acidic optimum pHs to have a base/acid ratio smaller than one a

60 , it was strongly dependent upon pH, and the optimum pH value of 5.5 probably reflected the location

61 ificity constant k(cat)/K(m)(sulfite) at the optimum pH value of 8.25.

62 It was shown that the optimum pH values (pH of maximal stability) of the compl

63 The optimum pH values of quantitative biosorption for Co(2+)

64 y) of the complex tend to be the same as the optimum pH values of the complex components.

65 The optimum pH was 8.25 and the enzyme displayed a strong de

66 The optimum pH was determined in the numerical calculations

67 In many cases, the optimum pH was found at a pH corresponding to a large ne

68 or the pH of maximal stability (experimental optimum pH) was reproducible (rmsd = 0.73).

69 e their cargo will only be released when the optimum pH window is reached.