Yeung M K
Department of Pediatric Dentistry, University of Texas Health Science Center, San Antonio 78284.
Infect Immun. 1993 Jan;61(1):109-16. doi: 10.1128/iai.61.1.109-116.1993.
The nucleotide sequence of the Actinomyces viscosus T14V sialidase gene (nanH) and flanking regions was determined. An open reading frame of 2,703 nucleotides that encodes a predominately hydrophobic protein of 901 amino acids (M(r), 92,871) was identified. The amino acid sequence at the amino terminus of the predicted protein exhibited properties characteristic of a typical leader peptide. Five 12-amino-acid units that shared between 33 and 67% sequence identity were noted within the central domain of the protein. Each unit contained the sequence Ser-X-Asp-X-Gly-X-Thr-Trp, which is conserved among other bacterial and trypanosoma sp. sialidases. Thus, the A. viscosus T14V nanH gene and the other prokaryotic and eukaryotic sialidase genes evolved from a common ancestor. Southern hybridization analyses under conditions of high stringency revealed the existence of DNA sequences homologous to A. viscosus T14V nanH in the genomes of 18 strains of five Actinomyces species that expressed various levels of sialidase activity. The data demonstrate that the sialidase genes from divergent groups of Actinomyces spp. are highly conserved.
测定了粘性放线菌T14V唾液酸酶基因(nanH)及其侧翼区域的核苷酸序列。鉴定出一个2703个核苷酸的开放阅读框,其编码一个由901个氨基酸组成的主要为疏水性的蛋白质(分子量为92,871)。预测蛋白质氨基末端的氨基酸序列表现出典型前导肽的特征。在蛋白质的中央结构域内发现了五个12个氨基酸的单元,它们的序列同一性在33%至67%之间。每个单元都包含序列Ser-X-Asp-X-Gly-X-Thr-Trp,这在其他细菌和锥虫属唾液酸酶中是保守的。因此,粘性放线菌T14V nanH基因以及其他原核和真核唾液酸酶基因是从一个共同祖先进化而来的。在高严格条件下的Southern杂交分析显示,在表达不同水平唾液酸酶活性的五个放线菌属的18个菌株的基因组中存在与粘性放线菌T14V nanH同源的DNA序列。数据表明,来自不同放线菌属组的唾液酸酶基因高度保守。