Weak light emission patterns from lactic acid bacteria

Luminescence

Volumn 14, Issue 2, 1999, Pages 99-105

  Vogel, Reiner ^a   Süssmuth, Roland ^a  

^a UNIVERSITY OF HOHENHEIM   (Germany)

Author keywords

Enterococcus faecalis; Hydrogen peroxide; Low level chemiluminescence; Oxidative stress; Superoxide

Indexed keywords

AEROBIC BACTERIA; BACILLI; CHEMILUMINESCENCE; LACTIC ACID; OXIDATION; OXIDATIVE STRESS; OXYGEN; SUPEROXIDE DISMUTASE;

ACID GROUPS; AEROBIC GROWTH; BACTERIAL STRAINS; EMISSION PATTERN; ENTEROCOCCUS FAECALIS; LACTIC ACID BACTERIA; LOW LEVEL CHEMILUMINESCENCE; ON-LINE MEASUREMENT; SUPEROXIDES; WEAK LIGHTS;

HYDROGEN PEROXIDE;

BACTERIA (MICROORGANISMS); ENTEROCOCCUS FAECALIS;

CATALASE; HYDROGEN PEROXIDE; LACTIC ACID; SUPEROXIDE DISMUTASE;

ANIMAL; ARTICLE; CAMEL; CHEMOLUMINESCENCE; DRUG EFFECT; ENTEROCOCCUS FAECALIS; LACTOBACILLUS; LACTOCOCCUS; LEUCONOSTOC; METABOLISM; MICROBIOLOGY; MILK; OXYGEN CONSUMPTION; PHYSIOLOGY;

ANIMALS; CAMELS; CATALASE; CHEMILUMINESCENT MEASUREMENTS; ENTEROCOCCUS FAECALIS; HYDROGEN PEROXIDE; LACTIC ACID; LACTOBACILLUS; LACTOCOCCUS; LEUCONOSTOC; MILK; OXYGEN CONSUMPTION; SUPEROXIDE DISMUTASE;

EID: 0033085196     PISSN: 15227235     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1522-7243(199903/04)14:2<99::AID-BIO519>3.0.CO;2-7     Document Type: Article

References (30)

1. Allen RC. Chemiluminescence from eukaryotic and prokaryotic cells: reducing potential and oxygen requirements. Photochem Photobiol 1979;30:157-63.
2. Hunter DJ and Allen RC. Oxygen-dependent Streptococcus faecalis chemiluminescence: the importance of metabolism and medium composition. In: DeLuca MA, McElroy WD, editors. Bioluminescence and chemiluminescence. New York: Academic Press, 1981:31-42.
3. Tilbury RN and Quickenden TI. Spectral and time dependence studies of the ultraweak bioluminescence emitted by the bacterium Escherichia coli. Photochem Photobiol 1988;47:145-50.
4. Roth JA and Kaeberle ML. Chemiluminescence by Listeria monocytogenes. J Bacteriol 1980;144:752-7.
5. Vogel R and Süssmuth R. Interaction of bacterial cells with weak light emission from culture media. Bioelectrochem Bioenerg 1998;45:93-101.
6. Carlsson J, Nyberg G and Wrethen J. Hydrogen peroxide and superoxide formation in anaerobic broth media exposed to atmospheric oxygen. Appl Env Microbiol 1978;36:223-9.
7. Vogel R and Süssmuth R. Low level chemiluminescence from liquid culture media. (Submitted to J Appl Microbiol).
8. Vogel R and Süssmuth R. A model for generation of low level chemiluminescence from microbiological growth media and its depletion by bacterial cells. Bioelectrochem Bioenerg (in press).
9. Terzaghi BE and Sandine WE. Improved medium for lactic streptococci and their bacteriophages. Appl Microbiol 1975;29: 807-13.
10. DeMan JC, Rogosa M and Sharpe ME. A medium for the cultivation of lactobacilli. J Appl Bacteriol 1960;23:130-35.
11. Süssmuth R, Eberspächer J, Haag R and Springer W. Mikrobiologisch biochemisches Praktikum, 2. Aufl. Stuttgart: Thieme, 1999.
12. Vogel R and Süssmuth R. Involvement of the cell membrane in chemiluminescence patterns from bacterial cultures. Bioelectrochem Bioenerg 46:65-9.
13. Vogel R, Guo X and Süssmuth R. Chemiluminescence patterns from bacterial cultures undergoing bacteriophage-induced mass lysis. Bioelectrochem Bioenerg 46:59-64.
14. Condon S. Responses of lactic acid bacteria to oxygen. FEMS Microbiol Rev 1987;46:269-80.
15. Ritchey TW and Seeley HW. Distribution of cytochrome-like respiration in streptococci. J Gen Microbiol 1976;93:195-203.
16. Pritchard GG and Wimpenny JWT. Cytochrome formation, oxygen-induced proton extrusion and respiratory activity in Streptococcus faecalis var. zymogenes grown in the presence of haematin. J Gen Microbiol 1978;104:15-22.
17. Bryan-Jones DG, Whittenbury R. Haematin-dependent oxidative phosphorylation in Streptococcus faecalis. J Gen Microbiol 1969; 58:247-60.
18. Kaars Sijpesteijn A. Induction of cytochrome formation and stimulation of oxidative dissimilation by hemin in Streptococcus lactis and Leuconostoc mesenteroides. Antonie van Leeuwenhoek 1970;36:335-18.
19. Smalley AJ, Jahrling P and Van Denmark PJ. Molar growth yields as evidence for oxidative phosphorylation in Streptococcus faecalis strain 10C1. J Bacteriol 1968;96:1595-600.
20. Whittenbury R. Hydrogen peroxide formation and catalase activity in the lactic acid bacteria. J Gen Microbiol 1964;35:13-26.
21. Britton L, Malinowsky DP and Fridovich I. Superoxide dismutase and oxygen metabolism in Streptococcus faecalis and comparison with other organisms. J Bacteriol 1978;134:229-36.
22. Engesser DM and Hammes WP. Non-heme catalase activity of lactic acid bacteria. System Appl Microbiol 1994;17:11-19.
23. Dolin MD. The Streptococcus faecalis oxidases for reduced diphosphopyridine nucleotide: III. Isolation and properties of a flavin peroxidase for reduced diphosphopyridine nucleotide. J Biol Chem 1957;225:557-73.
24. Zitzelsberger W, Götz F and Schleifer KH. Distribution of superoxide dismutases, oxidases and NADH peroxidases in various streptococci. FEMS Microbiol Lett 1984;21:243-6.
25. Archibald FS and Fridovich I. Manganese and defenses against oxygen toxicity in Lactobacillus plantarum. J Bacteriol 1981;145: 442-51.
26. Gregory EM and Fridovich I. Induction of superoxide dismutase by molecular oxygen. J Bacteriol 1973;114:543-8.
27. Halliwell B and Gutteridge JMC. Free radicals in biology and medicine. Oxford: Clarendon Press, 1989.
28. Cadenas E. Yearly review: biological chemiluminescence. Photochem Photobiol 1984;40:823-30.
29. Götz F, Sedewitz B and Elstner EF. Oxygen utilization by Lactobacillus plantarum: I. Oxygen consuming reactions. Arch Microbiol 1980;125:209-14.
30. Götz F, Elstner EF, Sedewitz B and Lengfelder E. Oxygen utilization by Lactobacillus plantarum: II. Superoxide and superoxide dismutation. Arch Microbiol 1980;125:215-20.