TABLE 1.
Culture vol | Fungal strain | Observed ion (m/z) | Proposed assignmenta | Expected ion (m/z) | Chromatography retention times (min) in:
|
||
---|---|---|---|---|---|---|---|
Bio-Gelb | Reverse-phase-C18c | Size exclusionc | |||||
Large | 505, G184A-R, and G184A-S | 538.2d | Dimerum acid | 538.2 | 220–300 | 28–28.3 (4) | 31.0–33.6 (3) |
Small | 505 | 316.5 | Fusarinine (monomeric) | 316.5 | 200–300 | 3.8 | 15.2 |
505 | 538.2 | Dimerum acid | 538.2 | 220–300 | 27.9 | 27.2 | |
505 | 580.2 | Acetyldimerum acide | 580.2 | 200–290 | 35.2 | Not done | |
505 | 780.3 | Coprogen Be | 780.3 | 220–245 | 35.9 | 19.15 | |
505 | 794.4 | Methyl coprogen B | 794.4 | 200–240 | 37.1–37.5 (2) | 19.3–19.5 (2) |
All in the ferrated state.
A range of retention times is given for the Bio-Gel peaks because they are broad, and the indicated range represents the region that was pooled for the next chromatographic step.
Data are presented as the range of retention times recorded on different days with different preparations (number of different experiments) or as the retention time observed on a single chromatogram.
This component comprised the bulk of the second peak of 480-nm absorption eluting from the Bio-Gel P2 column and was present as the predominant component in all filtrates examined.
Tentative assignment.