生物加工过程
生物加工過程
생물가공과정
CHINESE JOURNAL OF BIOPROCESS ENGINEERING
2014年
6期
57-61
,共5页
夏军%许召贤%薄芳芳%冯小海%迟波%徐虹
夏軍%許召賢%薄芳芳%馮小海%遲波%徐虹
하군%허소현%박방방%풍소해%지파%서홍
聚二氨基丙酸%纯化%离子交换层析%反向色谱
聚二氨基丙痠%純化%離子交換層析%反嚮色譜
취이안기병산%순화%리자교환층석%반향색보
poly( L-diaminopropionic acid)%purification%ion-exchange chromatography%reversed-phase chromatography
ε聚赖氨酸生产菌株Streptomyces albulus PD 1可合成一种新型非蛋白质氨基酸均聚物聚二氨基丙酸,采用离子交换层析和反向色谱,对聚二氨基丙酸的分离纯化进行研究。离子交换层析柱选用DEAE Sepharose Fast Flow填料,50 mmol/L 磷酸盐缓冲液( pH 7?5)平衡上样,含0?5 mol/L NaCl的磷酸盐缓冲液( pH 7?5)洗脱,收集洗脱液用分子筛 Sephadex G 25除去磷酸盐缓冲液。然后用 C18反相色谱进一步纯化,流动相为 V (甲醇)/V(0?1%磷酸)=5/95。经过离子交换层析和反向色谱,纯化得到聚二氨基丙酸纯品,回收率为39?8%,样品纯度达98?4%,为后续的聚二氨基丙酸的深入研究奠定基础。
ε聚賴氨痠生產菌株Streptomyces albulus PD 1可閤成一種新型非蛋白質氨基痠均聚物聚二氨基丙痠,採用離子交換層析和反嚮色譜,對聚二氨基丙痠的分離純化進行研究。離子交換層析柱選用DEAE Sepharose Fast Flow填料,50 mmol/L 燐痠鹽緩遲液( pH 7?5)平衡上樣,含0?5 mol/L NaCl的燐痠鹽緩遲液( pH 7?5)洗脫,收集洗脫液用分子篩 Sephadex G 25除去燐痠鹽緩遲液。然後用 C18反相色譜進一步純化,流動相為 V (甲醇)/V(0?1%燐痠)=5/95。經過離子交換層析和反嚮色譜,純化得到聚二氨基丙痠純品,迴收率為39?8%,樣品純度達98?4%,為後續的聚二氨基丙痠的深入研究奠定基礎。
ε취뢰안산생산균주Streptomyces albulus PD 1가합성일충신형비단백질안기산균취물취이안기병산,채용리자교환층석화반향색보,대취이안기병산적분리순화진행연구。리자교환층석주선용DEAE Sepharose Fast Flow전료,50 mmol/L 린산염완충액( pH 7?5)평형상양,함0?5 mol/L NaCl적린산염완충액( pH 7?5)세탈,수집세탈액용분자사 Sephadex G 25제거린산염완충액。연후용 C18반상색보진일보순화,류동상위 V (갑순)/V(0?1%린산)=5/95。경과리자교환층석화반향색보,순화득도취이안기병산순품,회수솔위39?8%,양품순도체98?4%,위후속적취이안기병산적심입연구전정기출。
The ε?polylysine producing strain Streptomyces albulus PD?1 could synthesize a novel non?proteinic amino acid oligomer:poly ( L?diaminopropionic acid ) ( PDAP )?Ion?exchange and reversed?phase chromatography were used to study the purification conditions of PDAP?In the ion?exchange chromatography purification,DEAE?Sepharose Fast Flow was selected,50 mmol/L phosphate buffer was used as mobile phase and 0?5 mol/L NaCl in the phosphate buffer acted as elution?In the reversed?phase chromatography purification,ratio of methanol to 0?1% phosphoric acid was 5/95 ( V/V) and was used as the mobile phase?Pure PDAP sample was obtained by ion?exchange and reversed?phase chromatography, the recovery rate of the purification was 39?8%,and the purity of the sample was 98.4%.