A nutrient poor medium containing 100 mg l-1 yeast-extract, 400 mg 1-1
tryptone, 100 mg l-1 calcium chloride, 150 mg l-1 cycloheximide, 25 m
g l-1 Congo-red and 10 g l-1 agar (medium A) greatly reduced polysacch
aride production and permitted development of discrete bacterial colon
ies from soil dilutions of 10(-2) and greater; pentachloronitrobenzene
(5 mg l-1) suppressed the growth of actinomycetes. Colony counts of d
iverse strains of Rhizobium meliloti and other fast growing rhizobia o
n this medium were either significantly greater or did not differ from
those on traditionally-used nutrient-rich agar media. Medium A was ma
de partially selective for R. meliloti by the addition of 5 g l-1 sodi
um chloride (medium AS). The utility of medium AS for detection and di
rect isolation of R. meliloti from soil was demonstrated by using colo
ny blot hybridization in conjunction with a species-specific DNA probe
derived from nodH: strains SU47 and 1521 were readily recovered from
a field soil (deficient in native rhizobia of the same species) in num
bers which did not differ significantly from those used at inoculation
.