Kazunori Yamada

Prof. Dr. Kazunori Yamada

Department of Applied Molecular Chemistry, College of Industrial Technology, Nihon University, 1-2-1 Izumi-cho Narashino, Chiba 275-8575, Japan
orcid

Research Focus & Metrics

Academic Career Length

38Years (1989-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
13 April 2000 in Biomacromolecules
Verified
Journal Article
Closed access
Kazunori YamadaKazunori Yamada
Kazunori Yamada
TCTianhong Chen
Tianhong Chen
GKGuneet Kumar
Guneet Kumar
OVOleg Vesnovsky
Oleg Vesnovsky
LTL. D. Timmie Topoleski
L. D. Timmie Topoleski
GPGregory F. Payne
Gregory F. Payne

5 September 2008 in Biotechnology Progress
Verified
Journal Article
Closed access
PDF file
Kazunori YamadaKazunori Yamada
Kazunori Yamada
YAYuji Akiba
Yuji Akiba
TSTakashi Shibuya
Takashi Shibuya
AKAYUMI KASHIWADA
AYUMI KASHIWADA
KMKiyomi Matsuda
Kiyomi Matsuda
MHMitsuo Hirata
Mitsuo Hirata
Enzymatic removal of various phenol compounds from artificial wastewater was undertaken by the combined use of mushroom tyrosinase (EC 1.14.18.1) and chitosan beads as function of pH value, temperature, tyrosinase dose, and hydrogen peroxide-to-substrate ratio. Chitosan film incubated in a p-crersol+tyrosinase mixture had the main peaks at 400-470 nm assigned to chemically adsorbed quinone derivatives, which increased over the immersion time. These results indicate that removal of phenol compounds is caused by their tyrosinase-catalyzed oxidation to the corresponding quinone derivatives and the subsequent chemical adsorption on the chitosan film. The optimum conditions for quinone adsorption were determined to be pH 7 and 45 degrees C for p-cresol. Some alkyl-substituted phenol compounds were removed by adsorption of quinone derivatives enzymatically generated on the chitosan beads, and the % removal for p-cresol, 4-ethylphenol, 4-n-propylphenol, 4-n-butylphenol, and p-chlorophenol went up to 93%. In addition, 4-tert-butylphenol underwent tyrosinase-catalyzed oxidation in the presence of hydrogen peroxide. This procedure was applicable to removal of chlorophenols and alkyl-substituted phenols.

22 January 1998 in Langmuir
Verified
Journal Article
Closed access
EKEtsuo Kokufuta
Etsuo Kokufuta
HSHironori Suzuki
Hironori Suzuki
RYRyo Yoshida
Ryo Yoshida
Kazunori YamadaKazunori Yamada
Kazunori Yamada
MHMitsuo Hirata
Mitsuo Hirata
FKFumitake Kaneko
Fumitake Kaneko

1 December 2004 in Biosensors and Bioelectronics
Verified
Journal Article
Closed access
SKShigeru Kurosawa
Shigeru Kurosawa
MNMiki Nakamura
Miki Nakamura
JPJong-Won Park
Jong-Won Park
HAHidenobu Aizawa
Hidenobu Aizawa
Kazunori YamadaKazunori Yamada
Kazunori Yamada
MHMitsuo Hirata
Mitsuo Hirata

25 October 1992 in Journal of Applied Polymer Science
Verified
Journal Article
Closed access
PDF file
Kazunori YamadaKazunori Yamada
Kazunori Yamada
HTHideyo Tsutaya
Hideyo Tsutaya
STShigeaki Tatekawa
Shigeaki Tatekawa
MHMitsuo Hirata
Mitsuo Hirata

16 July 2003 in Journal of Applied Polymer Science
Verified
Journal Article
Closed access
PDF file
Kazunori YamadaKazunori Yamada
Kazunori Yamada
TNToshiaki Nakasone
Toshiaki Nakasone
RNRyoichi Nagano
Ryoichi Nagano
MHMitsuo Hirata
Mitsuo Hirata