Purification and characterization of agarases from a marine bacterium Vibrio sp. F-6
文献类型:期刊论文
作者 | Fu, Wandong1,2,3; Han, Baoqin1; Duan, Delin3; Liu, Wanshun1; Wang, Changhong1 |
刊名 | JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY
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出版日期 | 2008-08-01 |
卷号 | 35期号:8页码:915-922 |
关键词 | Purification Characterization Agarase Neoagarooligosaccharide Vibrio Sp |
ISSN号 | 1367-5435 |
DOI | 10.1007/s10295-008-0365-2 |
文献子类 | Article |
英文摘要 | Marine bacterium Vibrio sp. F-6, utilizing agarose as a carbon source to produce agarases, was isolated from seawater samples taken from Qingdao, China. Two agarases (AG-a and AG-b) were purified to a homogeneity from the cultural supernatant of Vibrio sp. F-6 through ammonium sulfate precipitation, Q-Sepharose FF chromatography, and Sephacryl S-100 gel filtration. Molecular weights of agarases were estimated to be 54.0 kDa (AG-a) and 34.5 kDa (AG-b) by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). The optimum pH values for AG-a and AG-b were about 7.0 and 9.0, respectively. AG-a was stable in the pH range of 4.0-9.0 and AG-b was stable in the pH range of 4.0-10.0. The optimum temperatures of AG-a and AG-b were 40 and 55 degrees C, respectively. AG-a was stable at temperature below 50 degrees C. AG-b was stable at temperature below 60 degrees C. Zn(2+), Mg(2+) or Ca(2+) increased AG-a activity, while Mn(2+), Cu(2+) or Ca(2+) increased AG-b activity. However, Ag(+), Hg(2+), Fe(3+), EDTA and SDS inhibited AG-a and AG-b activities. The main hydrolysates of agarose by AG-a were neoagarotetraose and neoagarohexaose. The main hydrolysates of agarose by AG-b were neoagarooctaose and neoagarohexaose. When the mixture of AG-a and AG-b were used, agarose was mainly degraded into neoagarobiose.; Marine bacterium Vibrio sp. F-6, utilizing agarose as a carbon source to produce agarases, was isolated from seawater samples taken from Qingdao, China. Two agarases (AG-a and AG-b) were purified to a homogeneity from the cultural supernatant of Vibrio sp. F-6 through ammonium sulfate precipitation, Q-Sepharose FF chromatography, and Sephacryl S-100 gel filtration. Molecular weights of agarases were estimated to be 54.0 kDa (AG-a) and 34.5 kDa (AG-b) by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). The optimum pH values for AG-a and AG-b were about 7.0 and 9.0, respectively. AG-a was stable in the pH range of 4.0-9.0 and AG-b was stable in the pH range of 4.0-10.0. The optimum temperatures of AG-a and AG-b were 40 and 55 degrees C, respectively. AG-a was stable at temperature below 50 degrees C. AG-b was stable at temperature below 60 degrees C. Zn2+, Mg2+ or Ca2+ increased AG-a activity, while Mn2+, Cu2+ or Ca2+ increased AG-b activity. However, Ag+, Hg2+, Fe3+, EDTA and SDS inhibited AG-a and AG-b activities. The main hydrolysates of agarose by AG-a were neoagarotetraose and neoagarohexaose. The main hydrolysates of agarose by AG-b were neoagarooctaose and neoagarohexaose. When the mixture of AG-a and AG-b were used, agarose was mainly degraded into neoagarobiose. |
学科主题 | Biotechnology & Applied Microbiology |
URL标识 | 查看原文 |
语种 | 英语 |
WOS记录号 | WOS:000257945700015 |
公开日期 | 2010-12-24 |
源URL | [http://ir.qdio.ac.cn/handle/337002/5547] ![]() |
专题 | 海洋研究所_实验海洋生物学重点实验室 |
作者单位 | 1.Ocean Univ China, Coll Marine Life Sci, Qingdao 266003, Peoples R China 2.Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China 3.Chinese Acad Sci, Inst Oceanol, Qingdao 266071, Peoples R China |
推荐引用方式 GB/T 7714 | Fu, Wandong,Han, Baoqin,Duan, Delin,et al. Purification and characterization of agarases from a marine bacterium Vibrio sp. F-6[J]. JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY,2008,35(8):915-922. |
APA | Fu, Wandong,Han, Baoqin,Duan, Delin,Liu, Wanshun,&Wang, Changhong.(2008).Purification and characterization of agarases from a marine bacterium Vibrio sp. F-6.JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY,35(8),915-922. |
MLA | Fu, Wandong,et al."Purification and characterization of agarases from a marine bacterium Vibrio sp. F-6".JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY 35.8(2008):915-922. |
入库方式: OAI收割
来源:海洋研究所
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