Arrecubieta C, López R, García E
Departamento de Microbiología Molecular, Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas, Madrid, Spain.
J Bacteriol. 1994 Oct;176(20):6375-83. doi: 10.1128/jb.176.20.6375-6383.1994.
The complete nucleotide sequence of the cap3A gene of Streptococcus pneumoniae, which is directly responsible for the transformation of some unencapsulated, serotype 3 mutants to the encapsulated phenotype, has been determined. This gene encodes a protein of 394 amino acids with a predicted M(r) of 44,646. Twelve independent cap3A mutations have been mapped by genetic transformation, and three of them have been sequenced. Sequence comparisons revealed that cap3A was very similar (74.4%) to the hasB gene of Streptococcus pyogenes, which encodes a UDP-glucose dehydrogenase (UDP-GlcDH) that catalyzes the conversion of UDP-glucose to UDP-glucuronic acid, the donor substances in the pneumococcal type 3 capsular polysaccharide. Furthermore, a PCR-generated cap3A+ gene restored encapsulation in our cap3A mutants as well as in a mutant previously characterized as deficient in UDP-GlcDH (R. Austrian, H. P. Bernheimer, E.E.B. Smith, and G.T. Mills, J. Exp. Med. 110:585-602, 1959). These results support the conclusion that cap3A codes for UDP-GlcDH. We have also identified a region upstream of cap3A that should contain common genes necessary for the production of capsule of any type. Pulsed-field gel electrophoresis and Southern blotting showed that the capsular genes specific for serotype 3 are located near the genes encoding PBP 2X and PBP 1A in the S. pneumoniae chromosome, whereas copies of the common genes (or part of them) appear to be present in different locations in the genome.
肺炎链球菌cap3A基因的完整核苷酸序列已被确定,该基因直接负责将一些未被包囊的3型突变体转化为被包囊的表型。这个基因编码一个由394个氨基酸组成的蛋白质,预测分子量为44,646。通过遗传转化对12个独立的cap3A突变进行了定位,其中3个已进行测序。序列比较显示,cap3A与化脓性链球菌的hasB基因非常相似(74.4%),hasB基因编码一种UDP-葡萄糖脱氢酶(UDP-GlcDH),催化UDP-葡萄糖转化为UDP-葡萄糖醛酸,这是肺炎球菌3型荚膜多糖中的供体物质。此外,通过PCR产生的cap3A+基因在我们的cap3A突变体以及先前被鉴定为UDP-GlcDH缺陷的突变体中恢复了包囊化(R. Austrian, H. P. Bernheimer, E.E.B. Smith, and G.T. Mills, J. Exp. Med. 110:585-602, 1959)。这些结果支持cap3A编码UDP-GlcDH的结论。我们还在cap3A上游鉴定了一个区域,该区域应包含产生任何类型荚膜所需的共同基因。脉冲场凝胶电泳和Southern印迹显示,3型特异性的荚膜基因位于肺炎链球菌染色体中编码PBP 2X和PBP 1A的基因附近,而共同基因(或其部分)的拷贝似乎存在于基因组的不同位置。