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用于鉴定海洋绿色超微型浮游植物的基于核糖体RNA的寡核苷酸探针。

Ribosomal RNA-based oligonucleotide probes to identify marine green ultraphytoplankton.

作者信息

Knauber D C, Berry E S, Fawley M W

机构信息

Department of Botany, North Dakota State University, Fargo 58105, USA.

出版信息

J Eukaryot Microbiol. 1996 Mar-Apr;43(2):89-94. doi: 10.1111/j.1550-7408.1996.tb04486.x.

Abstract

Oligonucleotide probes based on small subunit 18S rRNA variable region sequences, were designed and used to discriminate groups of marine green ultraphytoplankton of similar size and morphology. Hybridization of probes was visualized using a combination of biotinylated oligonucleotides and fluorescein labeled avidin. Increased fluorescent signal was generated by building a complex of biotinylated probe, fluorescein labeled avidin and biotinylated anti-avidin. Cells of one phylogenetic group were easily differentiated from morphologically similar cells of a different phylogenetic group. Design of specific probes allowed identification of Mantoniella squamata, Micromonas pusilla, Pseudoscourfieldia marina and the micromonadophyte clone CCMP1194. This technique should be readily adaptable to open ocean samples and should greatly facilitate the description and quantification of ultraphytoplankton in the open ocean.

摘要

基于小亚基18S rRNA可变区序列设计的寡核苷酸探针,被用于区分大小和形态相似的海洋绿色超微型浮游植物群体。使用生物素化寡核苷酸和荧光素标记抗生物素蛋白的组合来观察探针的杂交情况。通过构建生物素化探针、荧光素标记抗生物素蛋白和生物素化抗抗生物素蛋白的复合物产生增强的荧光信号。一个系统发育群体的细胞很容易与不同系统发育群体中形态相似的细胞区分开来。特异性探针的设计使得能够鉴定出鳞状曼托尼藻、微小单胞藻、滨海伪斯科菲尔德藻和微型单胞藻克隆CCMP1194。这项技术应该很容易适用于开阔海洋样本,并且应该极大地促进对开阔海洋中超微型浮游植物的描述和定量。

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