Wehmeier U F
Bergische Universität GH Wuppertal, Chemische Mikrobiologie, D-42097, Wuppertal, Germany.
FEMS Microbiol Lett. 2001 Apr 1;197(1):53-8. doi: 10.1111/j.1574-6968.2001.tb10582.x.
The fda gene of Streptomyces galbus DSM40480 encoding the fructose-1,6-bisphosphate aldolase (EC 4.1.2.13) was cloned, sequenced and characterised. The fda gene encodes a protein of 341 amino acids with a molecular mass of 36.5 kDa and belongs to the class II aldolases. When the S. galbus fda gene was expressed in the Escherichia coli fda(ts) mutant NP315, the growth defect of the strain was complemented at temperatures >35 degrees C. In Northern hybridisations, we identified an fda transcript of 1200 bp length. The transcript length indicates that the fda gene is transcribed from its own promoter. Attempts to isolate fda knock out mutants were not successful. Streptomyces lividans strains with a second copy of the fda gene were constructed and analysed.
克隆、测序并表征了来自黄色链霉菌DSM40480的编码果糖-1,6-二磷酸醛缩酶(EC 4.1.2.13)的fda基因。该fda基因编码一种由341个氨基酸组成、分子量为36.5 kDa的蛋白质,属于II类醛缩酶。当黄色链霉菌fda基因在大肠杆菌fda(ts)突变体NP315中表达时,该菌株的生长缺陷在温度>35℃时得到互补。在Northern杂交中,我们鉴定出一个长度为1200 bp的fda转录本。转录本长度表明fda基因是从其自身启动子转录的。分离fda基因敲除突变体的尝试未成功。构建并分析了带有fda基因第二个拷贝的变铅青链霉菌菌株。