Sanangelantoni A M, Barbarini D, Di Pasquale G, Cammarano P, Tiboni O
Dipartimento di Genetica e Microbiologia A. Buzzati Traverso, Pavia, Italy.
Mol Gen Genet. 1990 Apr;221(2):187-94. doi: 10.1007/BF00261719.
The glnA gene of the thermophilic sulphur-dependent archaebacterium Sulfolobus solfataricus was identified by hybridization with the corresponding gene of the cyanobacterium Spirulina platensis and cloned in Escherichia coli. The nucleotide sequence of the 1696 bp DNA fragment containing the structural gene for glutamine synthetase was determined, and the derived amino acid sequence (471 residues) was compared to the sequences of glutamine synthetases from eubacteria and eukaryotes. The homology between the archaebacterial and the eubacterial enzymes is higher (42%-49%) than that found with the eukaryotic counterpart (less than 20%). This was true also when the five most conserved regions, which it is possible to identify in both eubacterial and eukaryotic glutamine synthetases, were analysed.
嗜热硫依赖古细菌嗜热栖热菌的谷氨酰胺合成酶基因(glnA)通过与蓝细菌钝顶螺旋藻的相应基因杂交得以鉴定,并克隆到大肠杆菌中。测定了包含谷氨酰胺合成酶结构基因的1696 bp DNA片段的核苷酸序列,并将推导的氨基酸序列(471个残基)与真细菌和真核生物的谷氨酰胺合成酶序列进行了比较。古细菌酶与真细菌酶之间的同源性(42%-49%)高于与真核生物对应酶的同源性(小于20%)。当分析真细菌和真核生物谷氨酰胺合成酶中均可识别的五个最保守区域时,情况也是如此。