Long-term nutrient starvation of continuously cultured (glucose-limited) Selenomonas ruminantium

Selenomonas ruminantium, a strictly anaerobic ruminal bacterium, was grown at various dilution rates (D = 0.05, 0.25, and 0.35 h-1) under glucose-limited continuous culture conditions. Suspensions of washed cells prepared anaerobically in mineral buffer were subjected to nutrient starvation (24 to 36 h; 39 degrees C; N2 atmosphere). Regardless of growth rate, viability declined logarithmically, and within about 2.5 h, about 50% of the populations were nonviable. After 24 h of starvation, the numbers of viable cells appeared to be inversely related to growth rate, the highest levels occurring with the slowest grown population. Cell dry weight, carbohydrate, protein, ribonucleic acid (RNA), and deoxyribonucleic acid declined logarithmically during starvation, and the decline rates of each were generally greater with cells grown at higher D values. Both cellular carbohydrate and RNA declined substantially during the first 12 h of starvation. Most of the cellular RNA that disappeared was found in the suspending buffer as low-molecular-weight, orcinol-positive materials. During growth, S. ruminantium made a variety of fermentation acids from glucose, but during starvation, acetate was the only acid made from catabolism of cellular material. Addition of glucose or vitamins to starving cell suspensions did not decrease loss of viability, whereas a starvation in the spent culture medium resulted in a slight decrease in the rate of viability loss. Overall, the data indicate that S. ruminantium strain D has very little survival capacity under the conditions tested compared with other bacterial species that have been studied.

[1]  J. Postgate,et al.  The Survival of vegetative microbes : twenty-sixth symposium of the Society for General Microbiology held at Lady Mitchell Hall, the University of Cambridge, April, 1976 , 1976 .

[2]  R. D. Batt,et al.  Survival of Nocardia corallina and Degradation of Constituents during Starvation , 1973 .

[3]  E. Dawes,et al.  Studies on the endogenous metabolism and senescence of starved Sarcina lutea. , 1967, The Biochemical journal.

[4]  R. D. Batt,et al.  Survival of Streptococcus lactis in starvation conditions. , 1968, Journal of general microbiology.

[5]  R. R. Johnson Influence of carbohydrate solubility on non-protein nitrogen utilization in the ruminant. , 1976, Journal of animal science.

[6]  D. E. Atkinson,et al.  Adenylate Energy Charge in Escherichia coli During Growth and Starvation , 1971, Journal of bacteriology.

[7]  H. R. Isaacson,et al.  Isolation and Characteristics of a Ureolytic Strain of Selenomonas ruminantium , 1974 .

[8]  A. H. Stouthamer,et al.  Molar growth yields and fermentation balances of Lactobacillus casei L3 in batch cultures and in continuous cultures. , 1970, Journal of general microbiology.

[9]  E. Dawes,et al.  Effect of starvation on the viability and cellular constituents of Zymomonas anaerobia and Zymomonas mobilis. , 1970, Journal of general microbiology.

[10]  O. H. Lowry,et al.  Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.

[11]  M. P. Bryant,et al.  An Improved Nonselective Culture Medium for Ruminal Bacteria and Its Use in Determining Diurnal Variation in Numbers of Bacteria in the Rumen , 1961 .

[12]  J. Sobek,et al.  Endogenous Metabolism of Azotobacter agilis , 1966, Journal of bacteriology.

[13]  A. Microbiology Survival of Starved Bacteria , 1967, Nature.

[14]  R. Strange Bacterial “Glycogen” and Survival , 1968, Nature.

[15]  R. D. Batt,et al.  Degradation of cell constituents by starved Streptococcus lactis in relation to survival. , 1969, Journal of general microbiology.

[16]  J. Breznak,et al.  Viability and Endogenous Substrates Used During Starvation Survival of Rhodospirillum rubrum , 1978, Journal of bacteriology.

[17]  J. van Houte,et al.  Role of Glycogen in Survival of Streptococcus mitis , 1970, Journal of bacteriology.

[18]  E. W. Crampton,et al.  The effect of change of ration on the required length of preliminary feeding period in digestion trials with sheep. , 1956 .

[19]  J. Leedle,et al.  Differential carbohydrate media and anaerobic replica plating techniques in delineating carbohydrate-utilizing subgroups in rumen bacterial populations , 1980, Applied and environmental microbiology.

[20]  W. J. Dixon,et al.  BMDP-79, biomedical computer programs, P-series , 1981 .

[21]  J. Nolan,et al.  Nitrogen cycling in sheep , 1973, Proceedings of the Nutrition Society.

[22]  F. Dark,et al.  The Survival of Stationary Phase Aerobacter aerogenes Stored in Aqueous Suspension , 1961 .

[23]  K. Burton A study of the conditions and mechanism of the diphenylamine reaction for the colorimetric estimation of deoxyribonucleic acid. , 1956, The Biochemical journal.

[24]  R. L. Baldwin,et al.  Comparison of Substrate Affinities Among Several Rumen Bacteria: a Possible Determinant of Rumen Bacterial Competition , 1979, Applied and environmental microbiology.

[25]  A. P. Harrison,et al.  PHENOTYPIC, GENOTYPIC, AND CHEMICAL CHANGES IN STARVING POPULATIONS OF AEROBACTER AEROGENES , 1963, Journal of bacteriology.

[26]  H. R. Isaacson,et al.  Efficiency of energy utilization by mixed rumen bacteria in continuous culture. , 1975, Journal of dairy science.

[27]  R. Wallace Cytoplasmic reserve polysaccharide of Selenomonas ruminantium , 1980, Applied and environmental microbiology.

[28]  M. P. Bryant,et al.  An anaerobic chemostat that permits the collection and measurement of fermentation gases. , 1973, Applied microbiology.

[29]  R. E. Hungate,et al.  The anaerobic mesophilic cellulolytic bacteria. , 1950, Bacteriological reviews.

[30]  E. Dawes,et al.  Fermentation of purines and their effect on the adenylate energy charge and viability of starved Peptococcus prévotii. , 1976, Journal of general microbiology.

[31]  M. P. Bryant,et al.  Commentary on the Hungate technique for culture of anaerobic bacteria. , 1972, The American journal of clinical nutrition.

[32]  N. Gibbons,et al.  Role and oxidation pathway of poly-beta-hydroxybutyric acid in Micrococcus halodenitrificans. , 1962, Canadian journal of microbiology.

[33]  J. Ensign Long-Term Starvation Survival of Rod and Spherical Cells of Arthrobacter crystallopoietes , 1970 .

[34]  D. W. Ribbons,et al.  The endogenous metabolism of microorganisms. , 1962, Annual review of microbiology.

[35]  J. Salanitro,et al.  Quantitative method for the gas chromatographic analysis of short-chain monocarboxylic and dicarboxylic acids in fermentation media. , 1975, Applied microbiology.

[36]  R. Moir,et al.  Ruminal flora studies. VIII. The influence of rate and method of feeding a ration upon its digestibility, upon ruminal function, and upon the ruminal population , 1957 .

[37]  R. B. Hespell,et al.  Ribonucleic acid destruction and synthesis during intraperiplasmic growth of Bdellovibrio bacteriovorus , 1975, Journal of bacteriology.

[38]  D. W. Ribbons,et al.  ENVIRONMENTAL AND GROWTH CONDITIONS AFFECTING THE ENDOGENOUS METABOLISM OF BACTERIA , 1963, Annals of the New York Academy of Sciences.

[39]  L. P. Milligan,et al.  Nitrogen metabolism in sheep , 1971, British Journal of Nutrition.

[40]  J. Campbell,et al.  NITROGENOUS SUBSTRATES OF ENDOGENOUS RESPIRATION IN PSEUDOMONAS AERUGINOSA , 1963, Journal of bacteriology.

[41]  R. Weller,et al.  Synthesis of microbial protein from ammonia in the sheep's rumen and the proportion of dietary nitrogen converted into microbial nitrogen , 1970, British Journal of Nutrition.

[42]  S. Pirt The maintenance energy of bacteria in growing cultures , 1965, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[43]  A. L. Koch,et al.  The adaptive responses of Escherichia coli to a feast and famine existence. , 1971, Advances in microbial physiology.

[44]  E. Dawes,et al.  The survival of Peptococcus prévotii in relation to the adenylate energy charge. , 1974, Journal of general microbiology.

[45]  A. L. Chaney,et al.  Modified reagents for determination of urea and ammonia. , 1962, Clinical chemistry.