Camara M, Mitchell T J, Andrew P W, Boulnois G J
Department of Microbiology, University of Leicester, United Kingdom.
Infect Immun. 1991 Aug;59(8):2856-8. doi: 10.1128/iai.59.8.2856-2858.1991.
A gene from Streptococcus pneumoniae was cloned in lambda EMBL301 and then expressed in Escherichia coli, which cleaved the fluorogenic neuraminidase substrate 2'-(4-methylumbelliferyl)-alpha-d-N-acetylneuraminic acid. The cloned gene therefore encodes an enzyme with neuraminidase activity. On the basis of restriction mapping and DNA hybridization studies, this gene could be distinguished from another pneumococcal neuraminidase gene cloned previously (A. M. Berry, J. C. Paton, E. M. Glare, D. Hansman, and D. E. A. Catcheside, Gene 71:299-305, 1988). Both neuraminidase genes were found in each of five isolates, covering at least three serotypes, of pneumococci tested.
将肺炎链球菌的一个基因克隆到λEMBL301中,然后在大肠杆菌中表达,该基因产物可切割荧光神经氨酸酶底物2'-(4-甲基伞形酮基)-α-D-N-乙酰神经氨酸。因此,克隆的基因编码一种具有神经氨酸酶活性的酶。根据限制性图谱分析和DNA杂交研究,该基因可与先前克隆的另一个肺炎球菌神经氨酸酶基因(A.M.贝里、J.C.帕顿、E.M.格拉尔、D.汉斯曼和D.E.A.卡奇赛德,《基因》71:299 - 305,1988年)区分开来。在所检测的至少三种血清型的五株肺炎球菌分离株中均发现了这两个神经氨酸酶基因。