首页> 外国专利> Bacterial restriction endonuclease prodn. - from antibiotic-sensitive Escherichia coli SB5 DSM N0.656

Bacterial restriction endonuclease prodn. - from antibiotic-sensitive Escherichia coli SB5 DSM N0.656

机译:细菌限制核酸内切酶产品-来自对抗生素敏感的大肠杆菌SB5 DSM N0.656

摘要

A new process is claimed for the prodn. of ECoRI restriction endonuclease from Escherichia Coli SB5 DMS No. 686, which has no antibiotic resistance but does have "ECo-RI". In this process, Escherichia coli SB5 is carried to the logarithmic phase under aerobic conditions in an aq. nutrient medium contg. proteins, inorganic salts and glycerine with aeration with air or O2-enriched air at 30-40 degrees C to produce a submerged culture from which the cell mass is centrifuged off. The cell mass is suspended at 0-4 degrees C in an aq. PEMA (10 mM KH2PO4K2HPO, pH 7.0, 0.7 mM mercaptoethanol, 1 mM EDFA) with ca 0.1 M NaCl and, opt., ca 0.2% non-ionic detergent and a part of the enzymatic activity is dissolved from the undisrupted cell mass by stirring with a shear force. The cell mass is centrifuged off and the supernatant is stirred with cetyltrimethylammonium bromide (end concn. 1 vol.%) to destroy undesired activities and the resulting ppte. is sepd. off and discarded. The supernatant is stirred with phosphocellulose, which is then washed with buffer contg. 0.1 M NaCl and eluted with buffer contg. 1 M NaCl. The eluate is dialysed against buffer contg. 0.1 M NaCl, then pumped onto a phosphocellulose column. The enzyme activity is bound to the column and the soln. is discarded. The column is eluted with a linear 0.3-0.8 M NaCl gradient and the eulate is collected in fractions. The fractions are tested, and those with ECo-RI activity are pumped onto a hydroxylapatite column. After washing with 0.1 M NaCl buffer, the column is eluted with a linear 0.01-0.5 M phosphate gradient, the eluate being collected in fractions. The fractions shown by testing to be active are conc. using a membrane tube to give highly pure conc. ECo-RI restriction endonuclease. ECo-RI restriction endonuclease can be used in the prodn. of recombinant DNA, which permits inclusion of new genetic information in bacteria. Appropriate choice of the DNA used can give bacteria capable of producing important natural products. The e. coli. strain used has no antibiotic resistance. It has been deposited in the German Collection of Microorganisms under the No. DSM 656.
机译:该产品要求一种新工艺。大肠杆菌EsRIichia Coli SB5 DMS No. 686的ECoRI限制性核酸内切酶的制备,它没有抗生素抗性,但确实具有“ ECo-RI”。在此过程中,将大肠杆菌SB5在好氧条件下于纯水中带入对数期。营养培养基续蛋白质,无机盐和甘油,然后在30-40摄氏度下与空气或富含O2的空气一起通气,以产生浸没的培养物,然后从中离心分离出细胞团。细胞团块悬浮在0-4℃的aq。水溶液中。 PEMA(10 mM KH2PO4K2HPO,pH 7.0,0.7 mM巯基乙醇,1 mM EDFA)含0.1 M NaCl和约0.2%非离子去污剂,一部分酶活性通过搅拌从未破碎的细胞团中溶解出来用剪切力。离心除去细胞团,并将上清液与十六烷基三甲基溴化铵(终浓度为1体积%)一起搅拌以破坏不希望的活性和所得的ppte。是sepd。关闭并丢弃。将上清液与磷酸纤维素一起搅拌,然后用浓缓冲液洗涤。 0.1 M NaCl并用连续缓冲液洗脱。 1 M氯化钠。用缓冲液补液对洗脱液进行透析。 0.1 M NaCl,然后泵送到磷酸纤维素柱上。酶活性与色谱柱和溶液结合。被丢弃。用线性0.3-0.8 M NaCl梯度洗脱柱子,并分馏收集洗脱液。测试级分,并将具有ECo-RI活性的级分泵送到羟磷灰石柱上。用0.1 M NaCl缓冲液洗涤后,用线性0.01-0.5 M磷酸盐梯度洗脱色谱柱,将洗脱液分馏收集。通过测试显示为有效的分数是一致的。使用膜管给予高度纯净的浓ECo-RI限制性核酸内切酶。 ECo-RI限制性核酸内切酶可用于该产品。重组DNA,可以在细菌中包含新的遗传信息。使用能给能够产生重要的天然产物的细菌DNA的合适的选择。 e。大肠杆菌。使用的菌株没有抗生素抗性。它已以DSM 656的形式存放在德国微生物收藏中。

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号