1987
DOI: 10.1016/s0176-6724(87)80197-9
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Relationship of bacteriocin-like inhibitor production to the pigmentation and hemolytic activity of mutans streptococci

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Cited by 9 publications
(7 citation statements)
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“…Only strain UA96 was hemolytic on blood agar. These observations are consistent with our previous ¢ndings [12] of an apparent lack of direct correlation between either pigmentation or hemolytic activity and bacteriocin production in mutans streptococci. Mutacin N activity eluted from the C8 reversed phase column at approximately 41% AcN and from the C18 reversed phase column at approximately 50% AcN suggesting that it is relatively hydrophobic.…”
Section: Resultssupporting
confidence: 93%
“…Only strain UA96 was hemolytic on blood agar. These observations are consistent with our previous ¢ndings [12] of an apparent lack of direct correlation between either pigmentation or hemolytic activity and bacteriocin production in mutans streptococci. Mutacin N activity eluted from the C8 reversed phase column at approximately 41% AcN and from the C18 reversed phase column at approximately 50% AcN suggesting that it is relatively hydrophobic.…”
Section: Resultssupporting
confidence: 93%
“…Crooks and coworkers [9] previously reported that strain D14 (group B) was haemolytic on human blood agar. Although not fully characterised, the association of bacteriocin production and haemolytic activity has been reported previously in some S. mutans [9] and S. salivarius [47]. The production of a protein that combines bacteriocin and haemolytic activity (bacteriocin/haemolysin) by E. faecalis strains is now well documented [48].…”
Section: Discussionmentioning
confidence: 99%
“…The haemolytic activity of both mutacin producers and non-producers was tested with double-layer agar plates consisting of a base layer of saline agar (NaCl 0.85% plus Davis agar 1.5%) and a top layer of Columbia agar base (CAB; Gibco BRL, Life Technologies, Paisley, Scotland) containing human blood 5% v/v [9]. Test colonies were inoculated into these plates with sterile tooth picks and incubated in an atmosphere of CO 2 5% in air at 378C for 48 h. Pigment production was assessed by visual examination of colonies for yellow pigmentation after anaerobic incubation for 2 days on TYCSB medium [30].…”
Section: Haemolytic Activity and Pigment Productionmentioning
confidence: 99%
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