High-intensity multiphoton free-free transitions.
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Biomedical subjects
Publications and source records attributed to G Ferrante.
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The lipids of a moderately halophilic methanogen, Methanococcus voltae, accounted for 5.1% of the cell dry weight and consisted of 91% polar lipids and 9% neutral lipids. Twelve polar lipids were detected, three of which, all derivatives of 2,3-di-O-phytanyl-sn-glycerol, were identified as: 2,3-di-O-phytanyl-1-O-[beta-D-glucopyranosyl-(1-6)-beta-D- glucopyranosyl]-sn-glycerol, 2,3-di-O-phytanyl-1-O-[beta-D-glucopyranosyl]-sn-glycerol and a novel NAc-glucosamine 1-phosphate diether, and 2,3-di-O-phytanyl-1-[phosphoryl-2-acetamido-2-deoxy-beta-D- glucopyranosyl]-sn-glycerol. The neutral lipids consisted mainly of squalenes: squalene, dihydrosqualene, tetrahydrosqualene, hexahydrosqualene, and unidentified squalenes.
Microsomal membranes prepared from Candida lipolytica cells grown at 10 degrees C had a higher lipid content and degree of unsaturation than membranes prepared from cells grown at 25 degrees C. The specific activities of stearoyl-CoA (18:0-CoA), oleoyl-CoA (18:1-CoA), and dioleoyl phosphatidylcholine (18:1-PC) desaturases in microsomes of cells grown at either 25 or 10 degrees C showed maximum values near midlog phase, coinciding with the respective maximum absolute content of linoleic (18:2) in the microsomal preparations. The 18:1-CoA desaturase activity in 10 degrees C cells was nearly double that in 25 degrees C cells, while the 18:0-CoA and 18:1-PC desaturases had considerably lower activities in 10 degrees C cells. An increase in aeration rate (shaking speed, 70 to 130 rpm) resulted in increased proportions of 18:2 (32 to 47%, respectively) in microsomes of cells grown at 25 degrees C and in increased 18:1-CoA desaturase specific activity (83 to 140 pmol X min-1 X mg-1); however, no significant changes occurred in 18:0-CoA or 18:1-PC desaturase activities.
Incubation of microsomes from 25 degrees C- or 10 degrees C-grown cells of Candida lipolytica with [14C]oleoyl-CoA ( [14C]18:1-CoA) in the presence or absence of NADH resulted in rapid acyl transfer of [14C]18:1 to phospholipids (mainly phosphatidylcholine (PC) and phosphatidylethanolamine (PE) and to acylglycerols. Incorporation into PC was greatly enhanced when incubation was carried out in presence of lysophosphatidylcholine (lyso-PC). In all experiments, in the presence of NADH and O2, with and without added lyso-PC, the initial rate of formation of [14C]linoleoyl-PC was much greater than that of [14C]linoleoyl-CoA ( [14C]18:2-CoA). These results suggest that the actual substrate for the delta 12-desaturase is the oleoyl-PC, although some desaturation of 18:1-CoA cannot be eliminated. It is concluded that the main pathway for 18:2 formation proceeds from stearoyl-CoA (18:0-CoA) leads to 18:1-CoA leads to 18:1-phospholipid leads to 18:2-phospholipid; the pathway 18:0-CoA leads to 18:1-CoA leads to 18:2-CoA leads to 18:2-phospholipid is a minor pathway. Microsomes from cells grown at 10 degrees C had a higher content of 18:2 and a lower phospholipid desaturase activity at 25 degrees C than microsomes from cells grown at 25 degrees C, suggesting an inverse relationship between desaturase activity and membrane lipid fluidity.
Seventeen cases of ischaemising phlebitis and 5 of venous gangrene are reported. Attention is given to the aetiopathogenetic factors that lead to massive thrombosis and dramatic progression of the disease: depression of vascular heparin, polyglobulia, serious dysproteinaemia, marked involvement of the arterial district, etc. Treatment may be medical or surgical, based on large doses of anticoagulants, low-weight dextrane and thrombolytic drugs, though the results expected are not always obtained. At present, early venous disobstruction with a Fogarty catheter, coupled with prolonged anticoagulant management is the best course. Prognosis is certainly better in ischaemia. When gangrene sets in, prognosis is particularly poor, even as far as survival is concerned, due to serious concomitant shock.
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