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Journal of Chromatography A | 1983

Thin-layer chromatographic analysis of carbapenem antibiotics in fermentation broths

Mitsuyasu Okabe; Kohki Kiyoshima; Ikuo Kojima; Rokuro Okamoto; Yasuo Fukagawa; Tomoyuki Ishikura

Abstract A one-dimensional silica gel thin-layer chromatographic method has been devised for qualitative and quantitative analysis of carbapenem antibiotics in fermentation broths. The antibiotics were extracted from the broth filtrate with a solvent mixture of 1-butanol and chloroform (1:1) and developed on a silica gel thin-layer plate with a mobile phase of acetonitrile—0.75% acetic acid (9:2). Carbapenem compounds on the thin-layer plate were visualized as reddish pink spots with the Ehrlich reagent and quantitated by densitometry.


Tetrahedron Letters | 1982

Structures of OA-6129A, B1, B2 and C, new carbapenem antibiotics

Takeo Yoshioka; Ikuo Kojima; Kunio Isshiki; Azuma Watanabe; Yasutaka Shimauchi; Mitsuyasu Okabe; Yasuo Fukagawa; Tomoyuki Ishikura

Abstract The structures of carbapenems OA-6129A, B 1 , B 2 and C were determined by spectroscopy and chemical transformation.


Journal of Fermentation and Bioengineering | 1990

Preferential production of a carbapenem antibiotic, PS-5 by dissolved oxygen controlled fermentation

Mitsuyasu Okabe; Ikuo Kojima; Shoji Azuma; Kazuo Takada; Yoshifumi Mutoh; Rokuro Okamoto; Katsuro Kubo; Yasuo Fukagawa; Kazuhiko Okamura; Tomoyuki Ishikura

Abstract As Streptomyces fulvoviridis A933-17M9 usually produces several carbapenem analogs including PS-5, the submerged fermentation conditions were optimized for preferential production of PS-5. The scale of PS-5 fermentation was expanded stepwise from a 2.5- l mini-jar fermentor to a 1500- l pilot-scale fermentor. For production of PS-5 as a major product among related carbapenem analogs, the concentration of dissolved oxygen during fermentation was controlled at levels where microbial conversion of PS-5 to epithienamycins A and C and further to MM17880 was largely prevented without deleterious influences on the carbapenem-biosynthesizing activity of mycelia.


The Journal of Antibiotics | 1994

Mer-NF5003B, E AND F, NOVEL SESQUITERPENOIDS AS AVIAN MYELOBLASTOSIS VIRUS PROTEASE INHIBITORS PRODUCED BY Stachybotrys sp.

Rei Kaneto; Kazuyuki Dobashi; Ikuo Kojima; Kazuya Sakai; Norio Shibamoto; Takeo Yoshioka; Hiroshi Nishida; Rokurou Okamoto; Hisayoshi Akagawa; Satoshi Mizuno


The Journal of Antibiotics | 1982

STUDIES ON THE OA-6129 GROUP OF ANTIBIOTICS, NEW CARBAPENEM COMPOUNDS

Mitsuyasu Okabe; Shoji Azuma; Ikuo Kojima; Kageaki Kouno; Rokuro Okamoto; Yasuo Fukagawa; Tomoyuki Ishikura


The Journal of Antibiotics | 1993

Mer-N5075A, A POTENTIAL HIV-1 PROTEASE INHIBITOR, PRODUCED BY Streptomyces chromofuscus

Rei Kaneto; Hiroyuki Chiba; Kazuyuki Dobashi; Ikuo Kojima; Kazuya Sakai; Norio Shibamoto; Hiroshi Nishida; Rokurou Okamoto; Hisayoshi Akagawa; Satoshi Mizuno


The Journal of Antibiotics | 1984

STRUCTURES OF OA-6129D AND E, NEW CARBAPENAM ANTIBIOTICS

Takeo Yoshioka; Azuma Watanabe; Ikuo Kojima; Yasutaka Shimauchi; Mitsuyasu Okabe; Yasuo Fukagawa; Tomoyuki Ishikura


The Journal of Antibiotics | 1994

A rapid and simple screening method for HIV-1 protease inhibitors using recombinant Escherichia coli

Rei Kaneto; Ikuo Kojima; Norio Shibamoto; Hiroshi Nishida; Rokuro Okamoto; Hisayoshi Akagawa; Satoshi Mizuno


Archive | 1989

DNA CODING FOR ENZYME CAPABLE OF ACYLATING THE 4"-POSITION OF MACROLIDE ANTIBIOTIC

Akira Arisawa; Naoto Kawamura; Ikuo Kojima; Yasushi Okumura; Kazuhiko Okamura; Hiroshi Tone; Rokuro Okamoto


The Journal of Antibiotics | 1988

Mutagenesis of OA-6129 carbapenem-producing blocked mutants and the biosynthesis of carbapenems.

Ikuo Kojima; Yasuo Fukagawa; Mitsuyasu Okabe; Tomoyuki Ishikura; Norio Shibamoto

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