3. Results and discussion
3.1. Isolation and identification of fungi
A total of 10 samples of soil were inoculated on a malt extract
agar medium containing chrysene. Among the 10 samples isolated,
20 fungi were selected for further screening by the method
described above. Six fungi that grewwell on the agar mediumwere
selectedamongthe 20. Other isolateswere discarded based on their
comparatively poor growth on agar medium containing chrysene.
Onefungus,namedS133,was found to bemost capable of degrading
chrysene. S133 has a cap with an indented cell similar to a honeycomb
white in color. Its stem is short, unequal, flared upward, and
bent with the cap. Its spore is white, grows in groups of several
specimens or in tuft of two or three individuals sometime with the
caps welded together, and has clamp connection between hyphae
[28,29]. Based on these macroscopic morphological characteristics,
S133 was identified as Polyporus sp. S133.
3. Results and discussion
3.1. Isolation and identification of fungi
A total of 10 samples of soil were inoculated on a malt extract
agar medium containing chrysene. Among the 10 samples isolated,
20 fungi were selected for further screening by the method
described above. Six fungi that grewwell on the agar mediumwere
selectedamongthe 20. Other isolateswere discarded based on their
comparatively poor growth on agar medium containing chrysene.
Onefungus,namedS133,was found to bemost capable of degrading
chrysene. S133 has a cap with an indented cell similar to a honeycomb
white in color. Its stem is short, unequal, flared upward, and
bent with the cap. Its spore is white, grows in groups of several
specimens or in tuft of two or three individuals sometime with the
caps welded together, and has clamp connection between hyphae
[28,29]. Based on these macroscopic morphological characteristics,
S133 was identified as Polyporus sp. S133.
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