8 research outputs found
Diversity of marine gliding bacteria in Thailand and their cytotoxicity
Eighty-four marine gliding bacteria were isolated from specimens
collected in the Gulf of Thailand and the Andaman Sea. All exhibited
gliding motility and swarm colonies on cultivation plates and they were
purified by subculturing and micromanipulator techniques. Their 16S
rRNA genes were amplified by the polymerase chain reaction (PCR)
technique. The phylogenetic analysis indicated that the represented
isolates can be separated into six different clads (gr 1 - gr 6) within
the Cytophaga-Flavobacterium-Bacteriodes (CFB) group. Group 1 formed a
remote linear, with only 90% sequence similarity, from
Flavobacteriaceae bacterium which indicated a potentially novel
taxonomic group. Groups 2 and 3 were identified as the recently
proposed Tenacibaculum mesophilum and Fulvivirga kasyanovii
respectively. Groups 4, 5 and 6, consisting of the largest number of
the members, were identified as Rapidithrix thailandica , Aureispira
marina and Aureispira maritima respectively. The isolates were
cultivated in four different cultivation media (Vy/2, RL 1, CY and SK)
and the crude extracts were submitted to screen cytotoxicity using a
sulphorodamine B (SRB) assay. The results from cytotoxic screening
showed that groups 2, 4 and 6 were capable of producing the cytotoxic
metabolites against selected human cell lines (breast adenocarcinoma
(MCF-7), colon cancer (HT-29), cervical cancer (HeLa) and oral cancer
(KB)). However, groups 1, 3 and 5 did not produce metabolites with
cytotoxicity when cultivated in the same cultivation media as the
previous groups. CY medium was the only cultivation medium which could
yield the cytotoxic metabolites against MCF-7
Diversity of marine gliding bacteria in Thailand and their cytotoxicity
Eighty-four marine gliding bacteria were isolated from specimens
collected in the Gulf of Thailand and the Andaman Sea. All exhibited
gliding motility and swarm colonies on cultivation plates and they were
purified by subculturing and micromanipulator techniques. Their 16S
rRNA genes were amplified by the polymerase chain reaction (PCR)
technique. The phylogenetic analysis indicated that the represented
isolates can be separated into six different clads (gr 1 - gr 6) within
the Cytophaga-Flavobacterium-Bacteriodes (CFB) group. Group 1 formed a
remote linear, with only 90% sequence similarity, from
Flavobacteriaceae bacterium which indicated a potentially novel
taxonomic group. Groups 2 and 3 were identified as the recently
proposed Tenacibaculum mesophilum and Fulvivirga kasyanovii
respectively. Groups 4, 5 and 6, consisting of the largest number of
the members, were identified as Rapidithrix thailandica , Aureispira
marina and Aureispira maritima respectively. The isolates were
cultivated in four different cultivation media (Vy/2, RL 1, CY and SK)
and the crude extracts were submitted to screen cytotoxicity using a
sulphorodamine B (SRB) assay. The results from cytotoxic screening
showed that groups 2, 4 and 6 were capable of producing the cytotoxic
metabolites against selected human cell lines (breast adenocarcinoma
(MCF-7), colon cancer (HT-29), cervical cancer (HeLa) and oral cancer
(KB)). However, groups 1, 3 and 5 did not produce metabolites with
cytotoxicity when cultivated in the same cultivation media as the
previous groups. CY medium was the only cultivation medium which could
yield the cytotoxic metabolites against MCF-7