Literature DB >> 1807202

Formation of fermentation products and extracellular protease during anaerobic growth of Bacillus licheniformis in chemostat and batch-culture.

B A Bulthuis1, C Rommens, G M Koningstein, A H Stouthamer, H W van Verseveld.   

Abstract

For a relaxed (rel-), protease producing (A-type) and a stringent (rel+), not-protease producing (B-type) variant of Bacillus licheniformis we determined fermentation patterns and products, growth parameters and alkaline protease-production (if any) in anaerobic, glucose-grown chemostats and batch-cultures. Glucose is dissimilated via glycolysis and oxidative pentose phosphate pathway simultaneously; the relative share of these two routes depends on growth phase (in batch) and specific growth rate (in chemostat). Predominant products are lactate, glycerol and acetaldehyde for A-type batches and acetaldehyde, ethanol, acetate and lactate for B-type batches. Both types show a considerable acetaldehyde production. In chemostat cultures, the fermentation products resemble those in batch-culture. From the anaerobic batches and chemostats, we conclude that the A-type (with low ATP-yield) will have a YATPmax of probably 12.9 g/mol and the B-type (with high ATP-yield) a YATPmax of about 10.1 g/mol. For batch-cultures, both types have about the same, high Yglucose (12 g/mol). So, the slow-growing A-type has a relatively high efficiency of anaerobic growth (i.e. an efficient use of ATP) and the fast-growing B-type a relatively low efficiency of anaerobic growth. In aerobic batch-cultures, we found 48, respectively 41% glucose-carbon conversion into mainly glycerol and pyruvate, respectively acetate as overflow metabolites in the A- and B-type. In both aerobic and anaerobic batch-cultures of the A-type, protease is produced predominantly in the logarithmic and early stationary phase, while a low but steady production is maintained in the stationary phase. Protease production occurs via de novo synthesis; up to 10% of the total protease in a culture is present in a cell-associated form. Although anaerobic protease production (expressed as protease per amount of biomass) is much higher than for aerobic conditions, specific rates of production are in the same range as for aerobic conditions while, most important, the substrate costs of anaerobic production are very much higher than for aerobic conditions.

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Year:  1991        PMID: 1807202     DOI: 10.1007/BF00430374

Source DB:  PubMed          Journal:  Antonie Van Leeuwenhoek        ISSN: 0003-6072            Impact factor:   2.271


  17 in total

1.  Comparative study of glucose catabolism by the radiorespirometric method.

Authors:  C H WANG; I STERN; C M GILMOUR; S KLUNGSOYR; D J REED; J J BIALY; B E CHRISTENSEN; V H CHELDELIN
Journal:  J Bacteriol       Date:  1958-08       Impact factor: 3.490

2.  Application of macroscopic principles to microbial metabolism.

Authors:  J A Roels
Journal:  Biotechnol Bioeng       Date:  2009-05-01       Impact factor: 4.530

3.  Bioflocculation as a microbial response to substrate limitations.

Authors:  B E Logan; J R Hunt
Journal:  Biotechnol Bioeng       Date:  1988-02-05       Impact factor: 4.530

4.  Production of Acetaldehyde by Zymomonas mobilis.

Authors:  M S Wecker; R R Zall
Journal:  Appl Environ Microbiol       Date:  1987-12       Impact factor: 4.792

5.  The role of iron and molecular oxygen in pulcherrimin synthesis by bacteria.

Authors:  D G Kupfer; R L Uffen; E Canale-Parola
Journal:  Arch Mikrobiol       Date:  1967-02-01

6.  Physiology of sporeforming bacteria associated with insects. I. Glucose catabolism in vegetative cells.

Authors:  L A Bulla; G St Julian; R A Rhodes; C W Hesseltine
Journal:  Can J Microbiol       Date:  1970-04       Impact factor: 2.419

7.  Bacitracin and protease production in relation to sporulation during exponential growth of Bacillus licheniformis on poorly utilized carbon and nitrogen sources.

Authors:  G W Hanlon; N A Hodges
Journal:  J Bacteriol       Date:  1981-08       Impact factor: 3.490

8.  The role of energy-spilling reactions in the growth of Klebsiella aerogenes NCTC 418 in aerobic chemostat culture.

Authors:  O M Neijssel; D W Tempest
Journal:  Arch Microbiol       Date:  1976-11-02       Impact factor: 2.552

9.  Generation of an electrochemical proton gradient in Streptococcus cremoris by lactate efflux.

Authors:  R Otto; A S Sonnenberg; H Veldkamp; W N Konings
Journal:  Proc Natl Acad Sci U S A       Date:  1980-09       Impact factor: 11.205

10.  Fermentation of glucose, lactose, galactose, mannitol, and xylose by bifidobacteria.

Authors:  W de Vries; A H Stouthamer
Journal:  J Bacteriol       Date:  1968-08       Impact factor: 3.490

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  1 in total

1.  The relation of proton motive force, adenylate energy charge and phosphorylation potential to the specific growth rate and efficiency of energy transduction in Bacillus licheniformis under aerobic growth conditions.

Authors:  B A Bulthuis; G M Koningstein; A H Stouthamer; H W van Verseveld
Journal:  Antonie Van Leeuwenhoek       Date:  1993-01       Impact factor: 2.271

  1 in total

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