Table 1.
Phospholipids and cholesterol in the cell membrane of representative Mycoplasma species.
Mycoplasma species | PL | C | CE | C/PL (molar ratio) | Reference |
---|---|---|---|---|---|
(nmole/mg membrane protein) | |||||
M. hyorhinis | 205.0 | 235.3 | 51.7 | 1.15 | — |
M. penetrans | 125.5 | 157.1 | 22.3 | 1.25 | [12] |
M. fermentans | 203.5 | 150.0 | 50.0 | 0.99 | [13] |
M. gallisepticum | 167.0 | 76.0 | 4.7 | 0.48 | [14] |
M. capricolum | 227.0 | 75.0 | 72.3 | 0.64 | [15] |
M. hyorhinis was grown in a modified Hayflick's medium [16] to the mid-exponential phase of growth, and isolated membranes were prepared as previously described [17]. Lipids were extracted from membrane preparations by the method of Bligh and Dyer [18]. Unesterified cholesterol, cholesterol esters, and phospholipids were separated on Merck Silica Gel G glass plates using benzene : diethyl ether : ethanol : acetic acid (50 : 40 : 2 : 0.2). The unesterified cholesterol and the cholesterol esters spots were extracted with chloroform for 30 min at room temperature, and the sterol content was determined by the phthaldialdehyde method [19]. Phosphorus in the phospholipid spot was determined by the method of Zhou and Arthur [20] using KH2PO4 as a standard. In brief, the spots were scraped from the plate into test tubes, digested with 0.5 mL of 70% perchloric acid (HClO4), and transferred into a 2 mL solution containing malachite green (0.2%) and ammonium molybdate (4%) in Tween-20 (1.5% w/v) and 5 M HCl (3 : 1 by vol.). The results are the average of three independent experiments using different batches of cells. PL: total phospholipids; TC: total cholesterol; C: unesterified cholesterol; CE: cholesterol esters.