Hatayama Kouta, Saito Katsumi
Sagami Chemical Research Institute, 2743-1 Hayakawa, Ayase, Kanagawa, 252-1193, Japan.
Department of Applied Chemistry, Tokai University, 4-1-1 Kitakaname, Hiratsuka, Kanagawa, 259-1292, Japan.
Antonie Van Leeuwenhoek. 2019 May;112(5):711-721. doi: 10.1007/s10482-018-1204-8. Epub 2018 Nov 21.
A wide range of bacterial species are able to induce calcium carbonate precipitation. Using our own laboratory-preserved strains, we have newly discovered that Ensifer sp. MY11e, Microbacterium sp. TMd9a1, Paeniglutamicibacter sp. MSa1a, Pseudomonas sp. GTc3, and Rheinheimera sp. ATWe6 can induce the formation of calcite crystals on an agar medium. Type strains of their closely related species (Ensifer adhaerens, Microbacterium testaceum, Paeniglutamicibacter kerguelensis, Pseudomonas protegens, and Rheinheimera texasensis) could also induce calcite formation. Although the initial pH value of the agar medium was 6.1, the pH of the agar media containing calcite, induced by cultivation of the 10 bacterial strains, increased to 8.0-8.4. The ammonification (oxidative deamination) of amino acids may been responsible for this increase in pH. The crystals formed both on and around the bacterial colonies. Furthermore, when these strains (excepting two Microbacterium strains) were cultivated on a cellulose acetate membrane filter (0.20 μm pore size) resting on the surface of the agar medium (i.e., in the membrane filter culture method), the crystals formed on the agar medium separate from the bacterial cells. These results indicate that the bacterial cells did not necessarily become nucleation sites for these crystals. We also investigated whether the studied strains could be applied to the biocementation of sand, and found that only two Ensifer strains were able to form large sand lumps.
多种细菌能够诱导碳酸钙沉淀。利用我们实验室保存的菌株,我们新发现中华根瘤菌属MY11e、微杆菌属TMd9a1、嗜谷氨酸杆菌属MSa1a、假单胞菌属GTc3和莱茵海默菌属ATWe6能够在琼脂培养基上诱导方解石晶体的形成。与其亲缘关系密切的物种(粘附中华根瘤菌、砖红微杆菌、克尔格伦嗜谷氨酸杆菌、荧光假单胞菌和德克萨斯莱茵海默菌)的模式菌株也能诱导方解石形成。尽管琼脂培养基的初始pH值为6.1,但由这10种细菌菌株培养诱导形成方解石的琼脂培养基的pH值升至8.0 - 8.4。氨基酸的氨化作用(氧化脱氨)可能是pH值升高的原因。晶体在细菌菌落上及其周围形成。此外,当这些菌株(除两种微杆菌菌株外)在置于琼脂培养基表面的醋酸纤维素膜过滤器(孔径0.20μm)上培养时(即采用膜过滤器培养法),琼脂培养基上形成的晶体与细菌细胞分离。这些结果表明,细菌细胞不一定是这些晶体的成核位点。我们还研究了所研究的菌株是否可用于沙子的生物胶结,发现只有两种中华根瘤菌菌株能够形成大的沙块。