植物学报
植物學報
식물학보
ACTA BOTANICA SINICA
2003年
3期
289-294
,共6页
吕玉兵%赵颖%赵剑锋%代小虎%仓怀兴%王耀萍%黄巨富
呂玉兵%趙穎%趙劍鋒%代小虎%倉懷興%王耀萍%黃巨富
려옥병%조영%조검봉%대소호%창부흥%왕요평%황거부
棕色固氮菌突变种UW3%固氮酶铬铁蛋白和锰铁蛋白%大单晶生长
棕色固氮菌突變種UW3%固氮酶鉻鐵蛋白和錳鐵蛋白%大單晶生長
종색고담균돌변충UW3%고담매락철단백화맹철단백%대단정생장
mutant UW3 of Azotobacter vinelandii%nitrogenase CrFe protein and MnFe protein%growth of large single crystals
用液/液扩散法, 从分别含Cr和Mn的无氨培养基中生长的固氮菌(Azotobacter vinelandii Lipmann)突变种UW3中纯化出的CrFe蛋白和MnFe蛋白, 在合适的结晶条件下生长出深棕色大单晶(最大晶体的尺寸分别为0.20 mm×0.20 mm×0.07 mm 和 0.18 mm×0.18 mm×0.05 mm).PEG、MgCl2和NaCl 的浓度对这两种蛋白的出晶时间、晶核数目、晶体大小和形状都有明显影响.结果表明,用此结晶法有利于CrFe蛋白和MnFe蛋白生长出可供X-射线衍射分析的大单晶.
用液/液擴散法, 從分彆含Cr和Mn的無氨培養基中生長的固氮菌(Azotobacter vinelandii Lipmann)突變種UW3中純化齣的CrFe蛋白和MnFe蛋白, 在閤適的結晶條件下生長齣深棕色大單晶(最大晶體的呎吋分彆為0.20 mm×0.20 mm×0.07 mm 和 0.18 mm×0.18 mm×0.05 mm).PEG、MgCl2和NaCl 的濃度對這兩種蛋白的齣晶時間、晶覈數目、晶體大小和形狀都有明顯影響.結果錶明,用此結晶法有利于CrFe蛋白和MnFe蛋白生長齣可供X-射線衍射分析的大單晶.
용액/액확산법, 종분별함Cr화Mn적무안배양기중생장적고담균(Azotobacter vinelandii Lipmann)돌변충UW3중순화출적CrFe단백화MnFe단백, 재합괄적결정조건하생장출심종색대단정(최대정체적척촌분별위0.20 mm×0.20 mm×0.07 mm 화 0.18 mm×0.18 mm×0.05 mm).PEG、MgCl2화NaCl 적농도대저량충단백적출정시간、정핵수목、정체대소화형상도유명현영향.결과표명,용차결정법유리우CrFe단백화MnFe단백생장출가공X-사선연사분석적대단정.
By using the liquid/liquid diffusion method at a suitable crystallization conditions, large single and dark brown crystals (the sides of the largest crystals were 0.20 mm×0.20 mm×0.07 mm and 0.18 mm×0.18 mm×0.05 mm, respectively) could be obtained from the solutions of nitrogenase CrFe protein and MnFe protein purified from a mutant UW3 of Azotobacter vinelandii Lipmann grown in Cr- or Mn-containing but NH3-free medium. The time of crystal formation, as well as the number, size, shape and quality of crystals obviously depended on the concentrations of PEG, MgCl2 and NaCl. The liquid/liquid diffusion method seems to benefit CrFe protein and MnFe protein for the growth of large single crystals for X-ray diffraction analysis.