Literature DB >> 16346292

Fermentation of Peptides by Bacteroides ruminicola B(1)4.

J B Russell1.   

Abstract

The maximum growth rate of Bacteroides ruminicola B(1)4 was significantly improved when either Trypticase or acetate and C(4)-C(5) fatty acids were added to defined medium containing macrominerals, microminerals, vitamins, hemin, cysteine hydrochloride, and glucose. The organism was unable to grow with peptides as the sole energy source, but growth yields from glucose were significantly improved when Trypticase was added to batch cultures containing basal medium, acetate, and C(4)-C(5) volatile fatty acids. During periods of rapid growth, very little peptide was deaminated to ammonia, but after growth ceased there was a linear increase in ammonia. Fifteen grams of Trypticase per liter resulted in maximum ammonia production. In glucose-limited chemostats, ammonia production from peptides was inversely proportional to the dilution rate, and 87% of the variation in ammonia production could be explained by retention time in the culture vessel. Chemostats receiving Trypticase had higher theoretical maximum growth yields and lower maintenance energy expenditures than similar cultures not receiving peptide. Cells from the Trypticase cultures contained more carbohydrate, and this difference was most evident at rapid dilution rates. When corrections were made for cell composition and the amount of peptides that were fermented, it appeared that peptide carbon skeletons could be used for maintenance energy. B. ruminicola B(1)4 was unable to grow on peptides alone because it was unable to utilize peptides at a fast enough rate to meet its maintenance requirement.

Entities:  

Year:  1983        PMID: 16346292      PMCID: PMC242502          DOI: 10.1128/aem.45.5.1566-1574.1983

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  35 in total

Review 1.  Quantitative aspects of nitrogen utilization in ruminants.

Authors:  J P Hogan
Journal:  J Dairy Sci       Date:  1975-08       Impact factor: 4.034

2.  Degradation of amino acids by pure cultures of rumen bacteria.

Authors:  C Scheifinger; N Russell; W Chalupa
Journal:  J Anim Sci       Date:  1976-10       Impact factor: 3.159

3.  The maintenance energy of bacteria in growing cultures.

Authors:  S J Pirt
Journal:  Proc R Soc Lond B Biol Sci       Date:  1965-10-12

4.  Effects of aldehyde treatment of soybean meal on in vitro ammonia release, solubility and lamb performance.

Authors:  A P Peter; E E Hatfield; F N Owens; U S Garrigus
Journal:  J Nutr       Date:  1971-05       Impact factor: 4.798

5.  Evidence for cytochrome involvement in fumarate reduction and adenosine 5'-triphosphate synthesis by Bacteroides fragilis grown in the presence of hemin.

Authors:  J Macy; I Probst; G Gottschalk
Journal:  J Bacteriol       Date:  1975-08       Impact factor: 3.490

6.  A theoretical study on the amount of ATP required for synthesis of microbial cell material.

Authors:  A H Stouthamer
Journal:  Antonie Van Leeuwenhoek       Date:  1973       Impact factor: 2.271

7.  Pathway of propionate formation in Bacteroides ruminicola.

Authors:  P Wallnöfer; R L Baldwin
Journal:  J Bacteriol       Date:  1967-01       Impact factor: 3.490

8.  Characterization of several bovine rumen bacteria isolated with a xylan medium.

Authors:  B A Dehority
Journal:  J Bacteriol       Date:  1966-05       Impact factor: 3.490

9.  Metabolism and growth yields in Bacteroides ruminicola strain b14.

Authors:  M R Howlett; D O Mountfort; K W Turner; A M Roberton
Journal:  Appl Environ Microbiol       Date:  1976-08       Impact factor: 4.792

10.  Specificity of the heme requirement for growth of Bacteroides ruminicola.

Authors:  D R Caldwell; D C White; M P Bryant; R N Doetsch
Journal:  J Bacteriol       Date:  1965-12       Impact factor: 3.490

View more
  19 in total

1.  Catabolism of Amino Acids by Megasphaera elsdenii LC1.

Authors:  R J Wallace
Journal:  Appl Environ Microbiol       Date:  1986-05       Impact factor: 4.792

2.  Effect of Dicarboxylic Acids and Aspergillus oryzae Fermentation Extract on Lactate Uptake by the Ruminal Bacterium Selenomonas ruminantium.

Authors:  D J Nisbet; S A Martin
Journal:  Appl Environ Microbiol       Date:  1990-11       Impact factor: 4.792

3.  More monensin-sensitive, ammonia-producing bacteria from the rumen.

Authors:  G Chen; J B Russell
Journal:  Appl Environ Microbiol       Date:  1989-05       Impact factor: 4.792

4.  Effect of hydrophobicity of utilization of peptides by ruminal bacteria in vitro.

Authors:  G Chen; H J Strobel; J B Russell; C J Sniffen
Journal:  Appl Environ Microbiol       Date:  1987-09       Impact factor: 4.792

5.  Enrichment and isolation of a ruminal bacterium with a very high specific activity of ammonia production.

Authors:  J B Russell; H J Strobel; G J Chen
Journal:  Appl Environ Microbiol       Date:  1988-04       Impact factor: 4.792

6.  Colonic proteolysis following pancreatic duct ligation in the rat.

Authors:  D Bustos; O Tiscornia; M I Caldarini; G Negri; S Pons; K Ogawa; J A De Paula
Journal:  Int J Pancreatol       Date:  1994-08

7.  Heat production by ruminal bacteria in continuous culture and its relationship to maintenance energy.

Authors:  J B Russell
Journal:  J Bacteriol       Date:  1986-11       Impact factor: 3.490

8.  Glucose toxicity in Prevotella ruminicola: methylglyoxal accumulation and its effect on membrane physiology.

Authors:  J B Russell
Journal:  Appl Environ Microbiol       Date:  1993-09       Impact factor: 4.792

9.  The NAD(P)H-dependent glutamate dehydrogenase activities of Prevotella ruminicola B(1)4 can be attributed to one enzyme (GdhA), and gdhA expression is regulated in response to the nitrogen source available for growth.

Authors:  Z Wen; M Morrison
Journal:  Appl Environ Microbiol       Date:  1996-10       Impact factor: 4.792

10.  In vitro ruminal fermentation of organic acids common in forage.

Authors:  J B Russell; P J Van Soest
Journal:  Appl Environ Microbiol       Date:  1984-01       Impact factor: 4.792

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.