Vd. Appanna et M. Stpierre, CELLULAR-RESPONSE TO A MULTIPLE-METAL STRESS IN PSEUDOMONAS-FLUORESCENS, Journal of biotechnology, 48(1-2), 1996, pp. 129-136
Pseudomonas fluorescens multiplied in a minimal mineral medium supplem
ented with millimolar amounts of aluminum (5 mM), iron (5 mM), zinc (3
mM), calcium (2 mM) and gallium (1 mM). A slight decrease in growth r
ate and a 22% diminution in cellular yield were observed as compared t
o the control medium. Citrate, the sole source of carbon to which the
test metals were complexed, was completely utilized. Although at stati
onary phase of growth most of the metals were immobilized in an exocel
lular lipid-rich residue, ultracentrifugation and dialysis studies rev
ealed that metals were associated with phosphatidylethanolamine (PE) f
rom early stages of growth. As growth progressed the metal content of
the soluble cellular extract increased reaching an optimum at 35 h of
incubation. However, no detectable amounts of metals in this cellular
component were discerned at stationary phase of growth. There appeared
to be no marked variation in exocellular protein and carbohydrate pro
duction in control and metal-stressed cultures. Transmission electron
microscopic studies revealed metal rich bodies associated with the cyt
oplasm. Scanning electron microscopic analyses of the dialyzate aided
in the identification of the metal-rich bodies associated with elongat
ed structures comprised of carbon, oxygen and phosphorus. PE appeared
to be an important organic constituent of the gelatinous residue.