Shiraishi Fumito, Zippel Barbara, Neu Thomas R, Arp Gernot
Geoscience Centre, University of Göttingen, Goldschmidtstrasse 3, D-37077 Göttingen, Germany.
J Microbiol Methods. 2008 Sep;75(1):103-8. doi: 10.1016/j.mimet.2008.05.015. Epub 2008 May 20.
Modified protocols of fluorescence in situ hybridization (FISH) and catalyze reporter deposition fluorescence in situ hybridization (CARD-FISH) were developed in order to detect bacteria in situ in calcified stromatolite biofilms. Smooth, well-preserved thin sections of calcified biofilms (approximately 5 microm thin, vertical sectioning of approximately 1 cm deep) were obtained by cryo-sectioning using the adhesive tape-stabilization technique. A modified hybridization buffer was applied during hybridization to prevent calcite dissolution as well as false binding of oligonucleotide probes to the charged mineral surfaces. Particularly, bright and specific CARD-FISH signals allowed the detection of bacteria in intensively calcified biofilms even at low magnification, which is suitable for investigating millimeter- to centimeter-scale vertical distribution patterns of bacteria.
为了在钙化叠层石生物膜中原位检测细菌,开发了荧光原位杂交(FISH)和催化报告沉积荧光原位杂交(CARD-FISH)的改进方案。使用胶带稳定技术通过冷冻切片获得钙化生物膜光滑、保存良好的薄片(约5微米厚,垂直切片深度约1厘米)。在杂交过程中使用了改良的杂交缓冲液,以防止方解石溶解以及寡核苷酸探针与带电矿物表面的错误结合。特别是,明亮且特异的CARD-FISH信号使得即使在低放大倍数下也能检测到高度钙化生物膜中的细菌,这适用于研究毫米至厘米尺度的细菌垂直分布模式。