Fluorescence resonance energy transfer (FRET)-based technique for tracking of endophytic bacteria in rice roots

Visualization of endophytes inside the host tissue has remained a prime interest to the plant microbiologist throughout the last decade. Assessment of a root colonization pattern of a nitrogen-fixing polyvalent plant-growth-promoting endophyte, Azotobacter chroococcum Avi2 (16S rRNA gene NCBI acc. n...

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Bibliographic Details
Published in:Biology and fertility of soils Vol. 52; no. 2; pp. 277 - 282
Main Authors: Banik, Avishek, Mukhopadhaya, Subhra Kanti, Sahana, Animesh, Das, Debasis, Dangar, Tushar Kanti
Format: Journal Article
Language:English
Published: Berlin/Heidelberg Springer Berlin Heidelberg 01-02-2016
Springer Nature B.V
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Summary:Visualization of endophytes inside the host tissue has remained a prime interest to the plant microbiologist throughout the last decade. Assessment of a root colonization pattern of a nitrogen-fixing polyvalent plant-growth-promoting endophyte, Azotobacter chroococcum Avi2 (16S rRNA gene NCBI acc. no. KP099933), of Oryza sativa var. Swarna , by a plasmid containing green fluorescent protein (GFP) gene failed because the bacteria formed a cyst on exposure to CaCl 2 during the transformation process of the green fluorescent protein gene. A new technique based on fluorescence resonance energy transfer (FRET) was developed to visualize the intracellular location of the bacterium of rice root as an alternative to track the bacterium where the use of GFP is restricted. An Al 3+ -specific rhodamine-based novel fluorescent ligand ( λ ex  = 400 nm, λ em  = 455 nm), (E)-3′,6′-bis(diethylamino)-2-(2-(pyren-4-ylmethyleneamino)ethyl)spiro[isoindoline-1,9′xanthen]-3-one, was synthesized and used to visualize 100 μM aluminium nitrate treated A. chroococcum inside rice root tissues. Within 6 h of incubation, a clear, stable and distinguishable green fluorescence was observed under the fluorescence microscope form Al 3+ -treated A. chroococcum colonized in the rice roots when incubated with a ligand. The results confirmed colonization of the bacteria inside the roots.
ISSN:0178-2762
1432-0789
DOI:10.1007/s00374-015-1064-6