Yoshimura M, Nakano Y, Yamashita Y, Oho T, Saito T, Koga T
Department of Preventive Dentistry, Kyushu University Faculty of Dental Science, Fukuoka 812-8582, Japan.
Infect Immun. 2000 Dec;68(12):6912-6. doi: 10.1128/IAI.68.12.6912-6916.2000.
Methyl mercaptan production by oral bacteria is thought to be one of the main causes of oral malodor. We examined the ability of periodontopathic Porphyromonas gingivalis to produce methyl mercaptan from L-methionine and found that the invasive strains W83 and W50 produced large amounts of methyl mercaptan. We cloned and sequenced the mgl gene encoding L-methionine-alpha-deamino-gamma-mercaptomethane-lyase (METase) from P. gingivalis W83. The structural mgl gene consisted of 1,200 bp and encoded a 43.3-kDa protein. To examine the role of methyl mercaptan in the pathogenesis of P. gingivalis, a METase-deficient mutant of P. gingivalis W83 was constructed. The methionine degradation activity and virulence of the mutant (M1217) and the parent strain (W83) in mice were compared. M1217 showed a marked decrease in the formation of methyl mercaptan from L-methionine and decreased virulence compared with the wild-type strain W83. These results suggest that methyl mercaptan not only is one of the sources of oral malodor, but may also play a role in the pathogenicity of P. gingivalis.
口腔细菌产生甲硫醇被认为是口臭的主要原因之一。我们检测了牙周病原菌牙龈卟啉单胞菌从L-甲硫氨酸产生甲硫醇的能力,发现侵袭性菌株W83和W50能产生大量甲硫醇。我们从牙龈卟啉单胞菌W83中克隆并测序了编码L-甲硫氨酸-α-脱氨基-γ-巯基甲烷裂解酶(METase)的mgl基因。mgl结构基因由1200 bp组成,编码一个43.3 kDa的蛋白质。为了研究甲硫醇在牙龈卟啉单胞菌致病机制中的作用,构建了牙龈卟啉单胞菌W83的METase缺陷突变体。比较了突变体(M1217)和亲本菌株(W83)在小鼠体内的甲硫氨酸降解活性和毒力。与野生型菌株W83相比,M1217从L-甲硫氨酸形成甲硫醇的能力显著降低,毒力也降低。这些结果表明,甲硫醇不仅是口臭的来源之一,而且可能在牙龈卟啉单胞菌的致病性中起作用。