This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Yamaguchi, N.
Right arrow Articles by Nasu, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Yamaguchi, N.
Right arrow Articles by Nasu, M.
Agricola
Right arrow Articles by Yamaguchi, N.
Right arrow Articles by Nasu, M.

 Previous Article  |  Next Article 

Appl. Environ. Microbiol., Jan 1996, 275-278, Vol 62, No. 1
Copyright © 1996, American Society for Microbiology

Detection of specific bacterial cells with 2-hydroxy-3-naphthoic acid- 2'-phenylanilide phosphate and fast red TR in situ hybridization

N Yamaguchi, S Inaoka, K Tani, T Kenzaka and M Nasu
Faculty of Pharmaceutical Sciences, Osaka University, Japan.

An in situ hybridization technique with HNPP (2-hydroxy-3-naphthoic acid-2'-phenylanilide phosphate) and Fast Red TR was used to detect specific bacterial cells at the single-cell level. By this technique, the fluorescent signals of target bacterial cells were up to eight times more intense than those of standard fluorescence in situ hybridization with mono-fluorescein isothiocyanate-labeled oligonucleotide probes. This novel HNPP-Fast Red TR whole-cell hybridization technique is available for the identification of small or low-rRNA-content bacterial cells in the natural environment.


This article has been cited by other articles:

  • Sunamura, M., Higashi, Y., Miyako, C., Ishibashi, J.-i., Maruyama, A. (2004). Two Bacteria Phylotypes Are Predominant in the Suiyo Seamount Hydrothermal Plume. Appl. Environ. Microbiol. 70: 1190-1198 [Abstract] [Full Text]  
  • Maruyama, F., Kenzaka, T., Yamaguchi, N., Tani, K., Nasu, M. (2003). Detection of Bacteria Carrying the stx2 Gene by In Situ Loop-Mediated Isothermal Amplification. Appl. Environ. Microbiol. 69: 5023-5028 [Abstract] [Full Text]  
  • Hoshino, T., Noda, N., Tsuneda, S., Hirata, A., Inamori, Y. (2001). Direct Detection by In Situ PCR of the amoA Gene in Biofilm Resulting from a Nitrogen Removal Process. Appl. Environ. Microbiol. 67: 5261-5266 [Abstract] [Full Text]  
  • Maruyama, A., Sunamura, M. (2000). Simultaneous Direct Counting of Total and Specific Microbial Cells in Seawater, Using a Deep-Sea Microbe as Target. Appl. Environ. Microbiol. 66: 2211-2215 [Abstract] [Full Text]  
  • Tani, K., Kurokawa, K., Nasu, M. (1998). Development of a Direct In Situ PCR Method for Detection of Specific Bacteria in Natural Environments. Appl. Environ. Microbiol. 64: 1536-1540 [Abstract] [Full Text]  
  • Paragas, V. B., Zhang, Y.-Z., Haugland, R. P., Singer, V. L. (1997). The ELF-97 Alkaline Phosphatase Substrate Provides a Bright, Photostable, Fluorescent Signal Amplification Method for FISH. J. Histochem. Cytochem. 45: 345-358 [Abstract] [Full Text]