Abstract :
Growth conditions of Magnetospirillum magneticum AMB-1 were optimized by orthogonal experimental design. When culturing conditions were chosen with ferric quinine 0.02 mmol/L, 75% volume, pH 6.7 and 25degC, the OD600 values reached 0.440 (1.166times109 cells/ml). AMB-1 cells were all collected by magnet before inoculation. After magnetic enrichment and cultivation for several times, Cmag values of AMB-1 reached 1.9- 2.0 steadily. During cultivating process, magnetosomes (MS) were characterized by Transmission Electron Microscope (TEM). As a result, smaller crystals (average 27.87 nm, n=188) were observed in bacteria after 24 h incubation. Over 48 h, the size of crystals increased (43.45 nm, n=203) and MS formed several chains arranging along major axes. After 72 h, crystals maturated (50.31 nm, n=191) and after 168 h, part-autolyzing bacteria with MS can be detected. Over 192 h, the bacteria autolyzed and MS were released to the media. It was also observed that two kinds of MS chain separating modes in dividing AMB-1 cells. One is symmetric separation into the daughter cells. The other is asymmetric separation and only one daughter cell was heritor of the MS. Part of non-magnetosome daughter cells might produce MS later.
Keywords :
biological techniques; biomagnetism; cellular biophysics; magnetic field effects; microorganisms; optimisation; transmission electron microscopy; AMB-1 cell cultivation; Magnetospirillum magneticum AMB-1 strain; asymmetric separation; daughter cell; ferric quinine; incubation; magnetic enrichment; magnetosome assembling; magnetotactic bacteria; orthogonal experimental design; part-autolyzing bacteria; symmetric separation; time 168 h; time 24 h; time 72 h; transmission electron microscope; Assembly; Crystals; Design for experiments; Design optimization; Magnetic field induced strain; Magnetic field measurement; Magnetic materials; Magnetic separation; Marine technology; Microorganisms;