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. 1998 Nov;180(21):5547–5558. doi: 10.1128/jb.180.21.5547-5558.1998

TABLE 2.

P oxidation phenotypes of plasmid-complemented P. stutzeri mutantsa

Plasmid Phenotypeb of strain:
WM581 [del3(BsiWI)]
WM691 [del2(SstI-KpnI)]
WM688 [del1(SstI-BsiWI)]
Hpt Pt Hpt Pt Hpt Pt
None +
pWM239 + + + + + +/−
pWM276 + + + + + +/−
pWM275 + + + + + +/−
pWM278 + + + + + +
pWM280 + + + +
pWM287 + + + +
pWM288 + + + +
pWM269 + +
pWM279 + +
pWM286 + +
pWM281 +
a

Strains tested were exconjugates of the indicated recipient P. stutzeri strains with E. coli S17-1 donors carrying the indicated broad-host-range plasmid. See Fig. 2 for the physical structure of each plasmid and Fig. 3 for the extents of the indicated deletions. 

b

Oxidation of reduced P compounds to phosphate was scored by testing each strain for growth on 0.4% glucose–MOPS medium with 0.5 mM hypophosphite (Hpt) or phosphite (Pt) as the sole P source. Because all organisms require phosphate, growth on these media is indicative of the ability to oxidize the P compound included as a P source. +, growth within 24 h at 37°C; +/−, growth within 72 h; −, no growth within 72 h. All strains tested grew in the identical medium supplemented with 0.5 mM phosphate.