GROWTH STIMULATOR FOR BIFIDOBACTERIA PRODUCED BY PROPIONIBACTERIUM-FREUDENREICHII AND SEVERAL INTESTINAL BACTERIA

Citation
T. Kaneko et al., GROWTH STIMULATOR FOR BIFIDOBACTERIA PRODUCED BY PROPIONIBACTERIUM-FREUDENREICHII AND SEVERAL INTESTINAL BACTERIA, Journal of dairy science, 77(2), 1994, pp. 393-404
Citations number
30
Categorie Soggetti
Agriculture Dairy & AnumalScience","Food Science & Tenology
Journal title
ISSN journal
00220302
Volume
77
Issue
2
Year of publication
1994
Pages
393 - 404
Database
ISI
SICI code
0022-0302(1994)77:2<393:GSFBPB>2.0.ZU;2-U
Abstract
A bifidogenic growth stimulator was present in the cell-free filtrate of Propionibacterium freudenreichii 7025 culture and in the methanol e xtract fraction of the cells. Several intestinal bacteria, such as Bac teroides, Enterobacter, and Enterococcus, which also released a growth stimulator for bifidobacteria, may play an important role in regulati on of a bifidobacterial population in colonic microflora. The water-so luble stimulator from the methanol extract of the cells was partially purified. The molecular weight of the stimulator appeared to be <3000. The stimulatory activity was unaffected by treatments with pronase, c arboxypeptidase A, ribonuclease, or nuclease P1 and was heat stable ov er a wide pH range. This stimulator differed from cyanocobalamin and f rom organic acids, such as acetate and propionate. Because it was stab le to heat and proteolytic enzymes, the stimulator is a useful bifidog enic factor that can reach the large intestine while retaining its act ivity. Short-chain fatty acids were highly inhibitory to the growth of many intestinal bacteria, particularly Gram-negative facultative and obligatory anaerobes. The short-chain fatty acids (especially propiona te) stimulated the growth of bifidobacteria. The growth of Bifidobacte rium adolescentis 6003 was further enhanced in the presence of short-c hain fatty acids and the stimulator produced by P. freudenreichii 7025 . Viable counts of strain 6003 grown with Bacteroides vulgatus JCM 582 6T increased more than 10(4) over those of the single culture of strai n 6003. However, the growth of strain 6003 was inhibited in the mixed culture with Clostridium perfringens 7028. In continuous culture, the growth of bifidobacterial strain 6003 could be greatly enhanced, even in the presence of clostridial strain 7028, in media with short-chain fatty acids and stimulator produced by P. freudenreichii 7025.