Conversion of Pneumococcal Inactive Amidase to the Active Form by Several Structural Analogues of Choline(Biological Chemistry)

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概要

• 論文の詳細を見る

• Several aminoalcohols (structural analogues of choline) were capable of converting the inactive form of pneumococcal autolysin to the active form in vitro. 2-dimethylaminoetHanoi, 3-dimethylamino-1-propanol, 2-diethylaminoethanol, and choline were most effective, but N-methyldiethanolamine, 2-ethylaminoethanol, and A-methylethanolamine were much less effective. The conversion of E-amidase to the active form by these aminoalcohols was observed at 37℃, in contrast to that by the enzyme substrate, cell walls containing choline, which required incubation at 0-4℃. All these aminoalcohols inhibited the hydrolytic activity of the active autolysin.

• 社団法人日本農芸化学会の論文
• 1990-05-23

著者

• SETO Hiroyuki

  Department of Periodontology and Endodontology, Institute of Health Bioscience, The University of To

• Shinagawa Akira

  Department Of Applied Biological Science Faculty Of Science And Technology Science University Of Tok

• Seto Hiroyuki

  Department Of Applied Biological Science Faculty Of Science And Technology Science University Of Tok

• Shinagawa A

  Science Univ. Tokyo Chiba Jpn

• KURASHIGE Yukiko

  Department of Applied Biological Science, Faculty of Science and Technology, Science University of T

• Kurashige Yukiko

  Department Of Applied Biological Science Faculty Of Science And Technology Science University Of Tok

• Seto Hiroyuki

  Department Of Applied Biological Science Faculty Of Science And Technology Science University Of Tok

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