Abstract
Immunological techniques can be applied to detect micro-organisms in different ecosystems. To follow the fate of Herbaspirillum seropedicae strain Z67 and H. rubrisubalbicans strain M4 in the rhizosphere of elephant grass, Pennisetum purpureum Schun. var. Capim Cana D'Africa, polyclonal antisera were raised against both strains. Both antisera were purified with protein-A, followed by a primary characterisation for cross-reactivity. To reduce cross-reactivity for both sera, affinity purification was used for improvement. After that, both sera could be considered as species specific. The detection limit was 105 cells ml-1 for the anti H. rubrisubalbicans serum and 106 cells ml-1 for the anti H. seropedicae serum. It was shown that two months after inoculation, both strains could be detected in the rhizoplane of elephant grass in high densities. The estimated numbers by ELISA were 107 cells g-1 fresh weight.
| Original language | English |
|---|---|
| Pages (from-to) | 139-150 |
| Number of pages | 12 |
| Journal | Symbiosis |
| Volume | 29 |
| Issue number | 2 |
| State | Published - 2000 |
| Externally published | Yes |
Keywords
- Diazotrophic bacteria
- Herbaspirillum
- Pennisetum purpureum
- Polyclonal antisera
Fingerprint
Dive into the research topics of 'Characterisation of different polyclonal antisera to quantify Herbaspirillum spp. in elephant grass (Pennisetum purpureum Schun.)'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver