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NEW ANTIBIOTIC ISTAMYCIN A1, B1, C1 OR A2

机译:新的抗生素ISTAMYC A1,B1,C1或A2

摘要

NEW MATERIAL:An antibiotic substance istamycin A1, B1, C1 or A2 expressed by formulaI(R1 is amino and R2 is H; or R1 is H and R2 is amino: R3 is HCO- or NH2CO-, R4 is methyl or ethyl) or an acid addition salt thereof. EXAMPLE:Istamycin A1 expressed by formula II. USE:An antimicrobial agent capable of inhibiting the growth of Gram-positive and Gram-negative bacteria with low toxicity. PROCESS:A microorganism, e.g. Streptomyces tenjimariensis SS-939 strain (FER M-P No.4932), capable of producing istamycin is inoculated into a culture medium containing nutrient sources utilizable by ordinary microorganisms, and cultivated aerobically by the spinner culture method in the liquid usually at 25-30 deg.C for 2-7 days. The aimed substance in the culture fluid is then adsorbed by various adsorbents, eluted, purified and separated by the thin layer chromatography, etc. to give the aimed istamycin A1, B1, C1 or A2.
机译:新材料:由式I表示的抗生素物质异霉素A1,B1,C1或A2(R 1为氨基,R 2为H;或R 1为H,R 2为氨基:R 3 >是HCO-或NH 2 CO-,R 4是甲基或乙基)或其酸加成盐。实施例:由式II表达的伊霉素A1。用途:一种能抑制革兰氏阳性菌和革兰氏阴性菌生长的低毒抗菌剂。过程:一种微生物,例如将能够产生异霉素的天链链霉菌SS-939菌株(FER MP No.4932)接种到含有可被普通微生物利用的营养源的培养基中,并通过旋转培养法在需氧条件下于液体中通常在25-30度下培养。 C持续2-7天。然后将培养液中的目标物质用各种吸附剂吸附,通过薄层色谱法等进行洗脱,纯化和分离,得到目标异霉素A1,B1,C1或A2。

著录项

  • 公开/公告号JPS57138651U

    专利类型

  • 公开/公告日1982-08-30

    原文格式PDF

  • 申请/专利权人

    申请/专利号JP19810024359U

  • 发明设计人

    申请日1981-02-23

  • 分类号B41J3/20;

  • 国家 JP

  • 入库时间 2022-08-22 14:24:53

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