Liy Y, Dan J, Tao H, Xuedong Z
Department of Oral Biology, College of Dentistry, University of Florida, Gainesville, FL, USA.
Oral Microbiol Immunol. 2008 Aug;23(4):315-9. doi: 10.1111/j.1399-302X.2008.00430.x.
The hydrolysis of urea by the urease enzymes of oral bacteria is believed to have a major impact on oral microbial ecology and to be intimately involved in oral health and diseases. Actinomyces naeslundii is a ureolytic bacterium that is adapted to tolerate the rapid and dramatic fluctuations in nutrient availability, carbohydrate source, and pH in dental biofilms. Our research objectives were to better understand the regulation of the expression of urease under environmental conditions that closely mimic those in dental biofilms.
A. naeslundii ATCC12104 were grown in a chemostat biofilm reactor with carbohydrate-limited medium for 3 days followed by a carbohydrate pulse, at pH 7.0 and at pH 5.5. Urease activities and ureC gene messenger RNA levels of cells in the biofilm were measured before and after the carbohydrate pulse.
We found that the neutral pH environments and excess carbohydrate availability could both result in enhancement of urease activity in biofilm cells. The ureC messenger RNA level of A. naeslundii biofilm cells cultivated at pH 7.0 was approximately 10-fold higher than that of cells grown at pH 5.5, but no changes in ureC gene expression were detected after the carbohydrate pulse.
Neutral pH environments and excess carbohydrate availability could promote urease expression of A. naeslundii in biofilms, but only neutral pH environments could up-regulate the ureC gene expression and the pH regulates ureC gene expression at a transcriptional level.
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有重大影响,并与口腔健康和疾病密切相关。内氏放线菌是一种尿素分解菌,能够适应牙菌斑中营养物质可用性、碳水化合物来源和pH值的快速剧烈波动。我们的研究目标是在更接近牙菌斑环境条件下,更好地了解脲酶表达的调控机制。
将内氏放线菌ATCC12104在恒化器生物膜反应器中,于pH 7.0和pH 5.5条件下,在碳水化合物受限的培养基中培养3天,随后进行碳水化合物脉冲处理。在碳水化合物脉冲前后,测量生物膜中细胞的脲酶活性和ureC基因信使RNA水平。
我们发现中性pH环境和过量的碳水化合物供应均可导致生物膜细胞中脲酶活性增强。在pH 7.0培养的内氏放线菌生物膜细胞的ureC信使RNA水平比在pH 5.5培养的细胞高约10倍,但在碳水化合物脉冲后未检测到ureC基因表达的变化。
中性pH环境和过量的碳水化合物供应可促进生物膜中内氏放线菌脲酶的表达,但只有中性pH环境可上调ureC基因表达,且pH在转录水平上调节ureC基因表达。