Department of Oral Biology, School of Dental Medicine, University at Buffalo, State University of New York, Buffalo, NY 14214, USA.
Mol Oral Microbiol. 2012 Aug;27(4):284-94. doi: 10.1111/j.2041-1014.2012.00644.x. Epub 2012 Mar 14.
Streptococcus gordonii is a common oral commensal bacterial species in tooth biofilm (dental plaque) and specifically binds to salivary amylase through the surface exposed amylase-binding protein A (AbpA). When S. gordonii cells are pretreated with amylase, amylase bound to AbpA facilitates growth with starch as a primary nutrition source. The goal of this study was to explore possible regulatory effects of starch, starch metabolites and amylase on the expression of S. gordonii AbpA. An amylase ligand-binding assay was used to assess the expression of AbpA in culture supernatants and on bacterial cells from S. gordonii grown in defined medium supplemented with 1% starch, 0.5 mg ml(-1) amylase, with starch and amylase together, or with various linear malto-oligosaccharides. Transcription of abpA was determined by reverse transcription quantitative polymerase chain reaction. AbpA was not detectable in culture supernatants containing either starch alone or amylase alone. In contrast, the amount of AbpA was notably increased when starch and amylase were both present in the medium. The expression of abpA was significantly increased (P < 0.05) following 40 min of incubation in defined medium supplemented with starch and amylase. Similar results were obtained in the presence of maltose and other short-chain malto-oligosacchrides. These results suggest that the products of starch hydrolysis produced from the action of salivary α-amylase, particularly maltose and maltotriose, up-regulate AbpA expression in S. gordonii.
戈登链球菌是牙菌斑(牙垢)中常见的口腔共生细菌种属,通过表面暴露的淀粉酶结合蛋白 A(AbpA)特异性结合唾液淀粉酶。当 S. gordonii 细胞用淀粉酶预处理时,与 AbpA 结合的淀粉酶促进以淀粉作为主要营养源的生长。本研究的目的是探索淀粉、淀粉代谢物和淀粉酶对 S. gordonii AbpA 表达的可能调控作用。采用淀粉酶配体结合测定法评估 AbpA 在 S. gordonii 培养上清液中的表达和在补充有 1%淀粉、0.5mg/ml 淀粉酶、淀粉和淀粉酶一起、或各种线性麦芽低聚糖的限定培养基中生长的细菌细胞上的表达。通过反转录定量聚合酶链反应测定 abpA 的转录。单独含有淀粉或淀粉酶的培养基中均检测不到 AbpA。相比之下,当培养基中同时存在淀粉和淀粉酶时,AbpA 的量明显增加。在补充有淀粉和淀粉酶的限定培养基中孵育 40 分钟后,abpA 的表达显著增加(P<0.05)。在存在麦芽糖和其他短链麦芽低聚糖的情况下也获得了相似的结果。这些结果表明,唾液α-淀粉酶作用下淀粉水解产生的产物,特别是麦芽糖和麦芽三糖,上调 S. gordonii 中 AbpA 的表达。