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唾液链球菌脲酶:基因与生化特性及在牙菌斑链球菌中的表达

Streptococcus salivarius urease: genetic and biochemical characterization and expression in a dental plaque streptococcus.

作者信息

Chen Y Y, Clancy K A, Burne R A

机构信息

Department of Dental Research, University of Rochester, New York 14642, USA.

出版信息

Infect Immun. 1996 Feb;64(2):585-92. doi: 10.1128/iai.64.2.585-592.1996.

Abstract

The hydrolysis of urea by urease enzyme of oral bacteria is believed to have a major impact on oral microbial ecology and to be intimately involved in oral health and diseases. To begin to understand the biochemistry and genetics of oral ureolysis, a study of the urease of Streptococcus salivarius, a highly ureolytic organism which is present in large numbers on the soft tissues of the oral cavity, has been initiated. By using as a probe a 0.6-kpb internal fragment of the S. salivarius 57.I ureC gene, two clones from subgenomic libraries of S. salivarius 57.I in an Escherichia coli plasmid vector were identified. Nucleotide sequence analysis revealed the presence of one partial and six complete open reading frames which were most homologous to ureIAB-CEFGD of other ureolytic bacteria. Plasmid clones were generated to construct a complete gene cluster and used to transform E. coli and Streptococcus gordonii DL1, a nonureolytic, dental plaque microorganism. The recombinant organisms expressed high levels of urease activity when the growth medium was supplemented with NiCl2. The urease enzyme was purified from E. coli, and its biochemical properties were compared with those of the urease produced by S. salivarius and those of the urease produced by S. gordonii carrying the plasmid-borne ure genes. In all cases, the enzyme had a Km of 3.5 to 4.1 mM, a pH optimum near 7.0, and a temperature optimum near 60 degrees C. S. gordonii carrying the urease genes was then demonstrated to have a significant capacity to temper glycolytic acidification in vitro in the presence of concentrations of urea commonly found in the oral cavity. The ability to genetically engineer plaque bacteria that can modulate environmental pH through ureolysis will open the way to using recombinant ureolytic organisms to test hypotheses regarding the role of oral ureolysis in dental caries, calculus formation, and periodontal diseases. Such recombinant organisms may eventually prove useful for controlling dental caries by replacement therapy.

摘要

口腔细菌的脲酶对尿素的水解作用被认为对口腔微生物生态具有重大影响,并与口腔健康和疾病密切相关。为了开始了解口腔尿素分解的生物化学和遗传学,已启动了对唾液链球菌脲酶的研究,唾液链球菌是一种高度尿素分解的生物体,大量存在于口腔软组织中。通过使用唾液链球菌57.I ureC基因的0.6-kpb内部片段作为探针,从唾液链球菌57.I在大肠杆菌质粒载体中的亚基因组文库中鉴定出两个克隆。核苷酸序列分析显示存在一个部分开放阅读框和六个完整开放阅读框,它们与其他尿素分解细菌的ureIAB-CEFGD最同源。构建了质粒克隆以构建完整的基因簇,并用于转化大肠杆菌和戈登链球菌DL1(一种非尿素分解的牙菌斑微生物)。当生长培养基中添加NiCl2时,重组生物体表达高水平的脲酶活性。从大肠杆菌中纯化了脲酶,并将其生化特性与唾液链球菌产生的脲酶以及携带质粒携带的ure基因的戈登链球菌产生的脲酶的生化特性进行了比较。在所有情况下,该酶的Km为3.5至4.1 mM,最适pH接近7.0,最适温度接近60℃。然后证明携带脲酶基因的戈登链球菌在口腔中常见的尿素浓度存在下,在体外具有显著的调节糖酵解酸化的能力。通过基因工程改造能够通过尿素分解调节环境pH的牙菌斑细菌的能力,将为使用重组尿素分解生物体来检验关于口腔尿素分解在龋齿、牙石形成和牙周疾病中的作用的假设开辟道路。这种重组生物体最终可能被证明可用于通过替代疗法控制龋齿。

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