著者

Takeuchi Setsuo Yonehara Hiroshi Umezawa Hamao

出版者

公益財団法人 日本感染症医薬品協会

雑誌

The Journal of Antibiotics, Series A (ISSN:03681173)

巻号頁・発行日

vol.12, no.5, pp.195-200, 1959

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<p>In the antibiotic screening studies directed by Prof. Sumiki, an antifungal substance was found in a culture filtrate of a fungus, No. K-5201, which was isolated from a soil collected at Karuizawa, Nagano Prefecture. The cultural characteristics of the strain No. K-5201 were investigated by Abe and others¹⁾. The strain was designated as <i>Paecilomyces varioti</i> Bainier var. <i>antibioticus</i>, and the antibiotic produced by this strain was named variotin.</p><p>Variotin is a new antifungal antibiotic, having low toxicity and exhibiting inhibition against <i>Trichophyton</i> and other pathogenic fungi. This paper describes processes of production, extraction and purification of variotin and its properties.</p>

著者

Teiichirō Itō Motohiro Nishio Hiroshi Ogawa

出版者

Japan Antibiotics Research Association

雑誌

The Journal of Antibiotics, Series A (ISSN:03681173)

巻号頁・発行日

vol.17, no.5, pp.189-193, 1964 (Released:2020-07-07)

参考文献数

14

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In the course of a research for kanamycin (kanamycin A)1) purification, kanamycin B1) and kanamycin C2) were isolated from the culture broth of Streptomyces kanamyceticus1). Kanamycin B was obtained in pure form by Schmitz, Fardig, O’Herron, Rousche and Hooper8), who isolated deoxystreptamine and 3-amino-3-deoxy-D-glucose after acid hydrolysis of N-acetyl-kanamycin B. Wakazawa, Sugano, Abe, Fukatsu and Kawaji4) reported that partial hydrolysis mixture of kanamycin B still retained some biological activity against B. subtilis, and later they5) isolated a crystalline degradation product which had antibacterial properties.It has been determined that in kanamycins A6,7,8,9) and C10) two aminosugars link to 4- and 6-positions of deoxystreptamine, while in neomycin-group (neomycins B C11,12d) and paromomycin13) the 4,5 hydroxyls of deoxystreptamine are substituted. It should be noted that neomycins are more toxic than kanamycins A and C. As compared with kanamycin A and neomycin S, kanamycin B has more than twice less toxicity than neomycins and has more than five times toxicity than kanamycin A. As reported by Wakazawa et. al.4), kanamycin B can be determined separately from A.In the present paper, our experiments on the structure of kanamycin B are described. Kanamycin B base, which was prepared by the process of Wakazawa et al4) and was recrystallized from ethanol-water, showed [α]24D+ 126° (c, 0.7 in water) and decomposed over the range of 170~190°C. It was soluble in water, but hardly soluble in organic solvent. Its molecular weight was reported to be 1,170 (Rast method, urea as solvent) by Schmitz et al.3) and 385~560 (Barger method, water as solvent) by Wakazawa et al.4) The crystals obtained in our laboratory showed molecular weight of 430~590 by the Rast method (urea as solvent, kanamycin A as standard).N-Acetylkanamycin B3,4) was prepared and, from its hydrolyzates, deoxystreptamine hydrochloride (molecular weight 235) was isolated in the yield of about 30% by weight. The elemental analyses of kanamycin B base and its N-acetyl derivative, together with the above data, suggested the molecular formula C18H37N5O10 for kanamycin B base.