Abstract:
Rice, being the most highly consumed cereal crop in Sri Lanka demand a
very high input of nitrogen fertilizer for cultivation. Use of nitrogen fertilizer
over a long period is known to cause many environmental and socio-economic problems. In the search of an alternative for nitrogen fertilizer,
Biological Nitrogen Fixation (BNF) is an excellent alternative. Successful
colonization of rice roots by a nitrogen-fixing bacterium is a prerequisite for
producing a nitrogen fixing rice plant. This study aims at inducing
colonization of Azorhizobium caulinodans ORS 571 in the roots of rice
variety BG 359 (i.e. cultivar popular in Sri Lanka) and determining the
optimum conditions for maximum efficiency of colonization, in terms of
inoculum volume, frequency of inoculation, best time interval for the
detection of the bacterium inside the rice plant in the presence of a signalling
molecule Naringenin. The bacterium A. caulinodans, being a free-living
nitrogen fixer, and having the ability to tolerate oxygen 3% v/v is
advantageous over other nitrogen fixers in non-symbiotic nitrogen fixation.
The bacterium was labelled with a green fluorescent protein marker (GFP)
for reliable and accurate detection in vivo. GFP- labelling was carried out by
inserting the gfp gene containing plasmid pBBR5-hem-gfp5-S65T into
Azorhizobium caulinodans ORS 571, with the help of a helper plasmid
(pRK2013) by tri parental mating. The degree of colonization was measured
through fluorescence of GFP by computer software (ZEN 2012). The
colonization increased up to the 25th day and then decreased giving very low
intensity measurements. It was revealed that 5ml (108
cells/ ml) of the
culture added twice a week for 15 days results in best conditions for
colonization by statistical analysis. Optimum conditions can be used for
future experiments of nitrogen fixation in rice.