首页> 外国专利> NEW ANTIBIOTIC SUBSTANCE AND PROCESS FOR THE EXTRACTION OF SUCH AN ANTIBIOTIC SUBSTANCE FORM A NEW STRAIN OF PSEUDOMONAS

NEW ANTIBIOTIC SUBSTANCE AND PROCESS FOR THE EXTRACTION OF SUCH AN ANTIBIOTIC SUBSTANCE FORM A NEW STRAIN OF PSEUDOMONAS

机译:一种新的抗菌物质及其提取方法-一种新的假单胞菌菌株的提取方法

摘要

1314019 Antibiotics from Pseudomocas Rollandi ALBERT ROLLAND SA 17 July 1970 [19 July 1969] 36428/69 Heading C2A In a process for producing an antibiotic whose infra-red spectrum is shown in Fig. 3, a strain of Pseudomonas Rollandi is aerobically cultured at 12-42‹ C., preferably 28‹ to 37‹ C., in a culture medium for a sufficient period of time to achieve the stationary growth phase of the Pseudomonas, the resulting Pseudomonas is then separated and ground, the resulting ground material is dehydrated, and the dehydrated material is extracted with methanol to give a methanolic solution of the crude antibiotic. The methanolic extract may be evaporated to dryness, extracted with a chlorinated solvent, e.g. chloroform, methylene chloride or trichloroacetic acid, followed by, or preceded by treatment with hexane or heptane to remove lipids. The resultant product may be extracted with ethanol to purify the antibiotic still further. The antibiotic comprises a peptide-ester or a depsipeptide component of average molecular weight 1000 to 2000, which can be isolated as slightly beige crystals, m.p. 155-156‹ C., D (measured at 20‹ C. in ethanol) = - 46 degrees and having the infra-red spectrum shown in Fig. 3 of the accompanying drawings and a second component which is a mixture or complex of dipeptide and in part depsi-peptide character, which can be isolated in a semi-crystalline, ninhydrinpositive form, which is soluble in dilute acetic acid and has an Rf of 0À35 on a cellulose plate when using the solvent system butanol-acetic acid-water, 12 : 3 : 5. Pharmaceutical compositions having antibiotic properties contain an antibiotic as described above in conjunction with a pharmaceutically acceptable excipient or carrier.
机译:假单胞菌Rollandi的1314019抗生素ALBERT ROLLAND SA 1970年7月17日[1969年7月19日] 36428/69标题C2A在生产图3所示红外光谱的抗生素的过程中,假单胞菌Rollandi菌株在12处进行有氧培养-42℃,最好是28℃至37℃,在培养基中放置足够长的时间以达到假单胞菌的稳定生长期,然后分离所得的假单胞菌并研磨,将所得的研磨材料脱水并用甲醇萃取脱水的物质,得到粗制抗生素的甲醇溶液。可以将甲醇提取物蒸发至干,用氯化溶剂,例如硫酸镁提取。氯仿,二氯甲烷或三氯乙酸,然后或之前,用己烷或庚烷处理以除去脂质。可以用乙醇提取所得产物以进一步纯化抗生素。该抗生素包含平均分子量为1000至2000的肽酯或二肽肽组分,可以分离为浅米色晶体,熔点为100-2000℃。 155-156℃,D(在20℃在乙醇中测量)=-46度,并具有附图图3所示的红外光谱,其第二组分是二肽的混合物或复合物。并具有部分depsi-peptide肽特性,可以分离为半结晶的茚三酮正离子形式,可溶于稀乙酸,并且在使用丁醇-乙酸-水溶剂体系时,在纤维素板上的Rf为0‑35, 12:3:5。具有抗生素特性的药物组合物包含上述抗生素以及药学上可接受的赋形剂或载体。

著录项

  • 公开/公告号ZA704837B

    专利类型

  • 公开/公告日1971-04-28

    原文格式PDF

  • 申请/专利权人 SA ROLLAND A SA;

    申请/专利号ZA19700004837

  • 发明设计人 GRANDPIERRE R;ROBERT A;

    申请日1970-07-14

  • 分类号C12K;

  • 国家 ZA

  • 入库时间 2022-08-23 10:12:26

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