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系统发育染色:用于单细胞鉴定的基于核糖体RNA的探针。

Phylogenetic stains: ribosomal RNA-based probes for the identification of single cells.

作者信息

DeLong E F, Wickham G S, Pace N R

机构信息

Department of Biology, Indiana University, Bloomington 47405.

出版信息

Science. 1989 Mar 10;243(4896):1360-3. doi: 10.1126/science.2466341.

Abstract

Rapid phylogenetic identification of single microbial cells was achieved with a new staining method. Formaldehyde-fixed, intact cells were hybridized with fluorescently labeled oligodeoxynucleotides complementary to 16S ribosomal RNA (rRNA) and viewed by fluorescence microscopy. Because of the abundance of rRNA in cells, the binding of the fluorescent probes to individual cells is readily visualized. Phylogenetic identification is achieved by the use of oligonucleotides (length 17 to 34 nucleotides) that are complementary to phylogenetic group-specific 16S rRNA sequences. Appropriate probes can be composed of oligonucleotide sequences that distinguish between the primary kingdoms (eukaryotes, eubacteria, archaebacteria) and between closely related organisms. The simultaneous use of multiple probes, labeled with different fluorescent dyes, allows the identification of different cell types in the same microscopic field. Quantitative microfluorimetry shows that the amount of an rRNA-specific probe that binds to Escherichia coli varies with the ribosome content and therefore reflects growth rate.

摘要

一种新的染色方法实现了对单个微生物细胞的快速系统发育鉴定。用甲醛固定的完整细胞与与16S核糖体RNA(rRNA)互补的荧光标记寡脱氧核苷酸杂交,然后通过荧光显微镜观察。由于细胞中rRNA含量丰富,荧光探针与单个细胞的结合很容易可视化。通过使用与系统发育组特异性16S rRNA序列互补的寡核苷酸(长度为为17至34个核苷酸)来实现系统发育鉴定。合适的探针可以由区分主要界(真核生物、真细菌、古细菌)以及密切相关生物体的寡核苷酸序列组成。同时使用用不同荧光染料标记的多种探针,可以在同一显微镜视野中鉴定不同的细胞类型。定量显微荧光测定法表明,与大肠杆菌结合的rRNA特异性探针的量随核糖体含量而变化,因此反映了生长速率。

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