2007
DOI: 10.1263/jbb.103.464
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Production of extracellular bifidogenic growth stimulator by anaerobic and aerobic cultivations of several propionibacterial strains

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Cited by 33 publications
(28 citation statements)
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“…al., , 2001(Taniguchi et. al., , 2005Kouya et al, 2007). As NPSI 38 consumed glucose gradually in the media, only lactic acid was produced corresponding to the consumption of glucose, and no other organic acids were detected throughout the cultivations, indicating that NPSI 38 is a typical homo-fermentative LAB.…”
Section: Resultsmentioning
confidence: 94%
“…al., , 2001(Taniguchi et. al., , 2005Kouya et al, 2007). As NPSI 38 consumed glucose gradually in the media, only lactic acid was produced corresponding to the consumption of glucose, and no other organic acids were detected throughout the cultivations, indicating that NPSI 38 is a typical homo-fermentative LAB.…”
Section: Resultsmentioning
confidence: 94%
“…This result implies that Bifidobacterium strains may produce a growth-promoting substance for EAggEC which is effective at neutral pH. Kouya et al [31] reported that several Propionibacterium strains produced an extracellular growth-stimulating substance for Bifidobacterium. Like the growth-promoting effect exerted by Bifidobacterium strains on EAggEC presented here, the growth-promoting activity exerted by Propionibacterium was only detected at pH 6.5-8.5.…”
Section: Discussionmentioning
confidence: 92%
“…Determination of the Inhibitory Effect of Culture Filtrate of Propionibacterial Strains on the Growth of H. pylori Propionibacterium acidipropionici JCM 6432 and P. jensenii JCM6433 were incubated in TPY medium as described previously [27], and culture filtrates of propionibacterial strains were prepared from the culture broths obtained after incubation for 48 hour. About 10 6 H. pylori cells were inoculated in a plate of Brucella agar (Becton Dickinson) containing 5% horse serum and 0.005% 2,3,5-triphenyltetrazorium chloride (Wako Pure Chemicals), and then a 200 lL of each culture filtrate of the propionibacterial strain, TPY medium, and 3 lg ⁄ mL of DHNA were added to a dish (5 mm in diameter) in the center of the Brucella agar plate.…”
Section: Determination Of Mic Of Dhna and Clarithromycinmentioning
confidence: 99%