Modelling the fed-batch production of pediocin using mussel processing wastes

Process Biochemistry

Volumn 40, Issue 3-4, 2005, Pages 1071-1083

  Guerra, Nelson P ^a   Agrasar, Ana Torrado ^a   Macías, Cristina López ^a   Pastrana, Lorenzo ^a  

^a UNIVERSITY OF VIGO   (Spain)

Author keywords

Fed batch fermentation; Homolactic fermentation; Mixed acid fermentation; Modelling; Mussel processing wastes; Pediocin

Indexed keywords

ALKALINITY; BIOMASS; CELL CULTURE; ETHANOL; NITROGEN; ORGANIC ACIDS; PH EFFECTS; PHOSPHORUS;

CELL GROWTH; LACTIC ACID; MUSSEL PROCESSING WASTES (MPW); PEDIOCIN;

FERMENTATION;

PEDIOCOCCUS; PEDIOCOCCUS ACIDILACTICI;

EID: 9644302727     PISSN: 00329592     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.procbio.2004.03.014     Document Type: Article

References (60)

1. Abee T., Krockel L., Hill C. Bacteriocins: modes of action and potentials in food preservation and control of food poisoning. Int. J. Food Microbiol. 28:1995;169-185
2. Tagg J.R., Dajani A.D., Wannamaker L.W. Bacteriocins of gram-positive bacteria. Bacteriol. Rev. 40:1976;722-756
3. Marugg J.D. Bacteriocins, their role in developing natural products. Food Biotechnol. 5:1991;305-312
4. Barefoot S.F., Nettles C.G. Antibiosis revisited: bacteriocins produced by dairy starter cultures. J. Dairy Sci. 76:1993;2366-2379
5. Bhunia A.K., Johnson M.C., Ray B. Purification, characterization and antimicrobial spectrum of a bacteriocin produced by Pediococcus acidilactici. J. Appl. Bacteriol. 65:1988;261-268
6. Kalchayanand N., Hanlin M.B., Ray B. Sublethal injury makes Gram-negative and resistant Gram-positive bacteria sensitive to the bacteriocins pediocin AcH and nisin. Lett. Appl. Microbiol. 15:1992;239-243
7. Kalchayanand N., Sikes T., Dunne C.P., Ray B. Hydrostatic pressure and electroporation have increased bactericidal efficiency in combination with bacteriocins. Appl. Environ. Microbiol. 60:1994;4174-4177
8. Delves-Broughton J., Blackburn P., Evans R.J., Hugenholtz J. Applications of the bacteriocin, nisin. Antonie van Leeuw. 69:1996;193-202
9. Soomoro A.H., Masud T., Anwaar K. Role of lactic acid bacteria (LAB) in food preservation and human health. A review. Pakistan J. Nutr. 1:2002;20-24
10. Parente E., Ricciardi A. Production, recovery and purification of bacteriocins from lactic acid bacteria. Appl. Microbiol. Biotechnol. 52:1999;628-638
11. Leroy F., De Vuyst L. Growth of bacteriocin-producing Lactobacillus sakei strain CTC 494 in MRS broth is strongly reduced due to nutrient exhaustion: a nutrient depletion model for the growth of lactic acid bacteria. Appl. Environ. Microbiol. 67:2001;4407-4413
12. a.P., Pastoriza L. Effects of aeration and pH gradient on nisin production. A mathematical model. Enzyme Microb. Technol. 29:2001;264-273
13. Guerra N.P., Rua M.L., Pastrana L. Nutritional factors affecting the production of two bacteriocins from lactic acid bacteria on whey. Int. J. Food Microbiol. 70:2001;271-285
14. Guerra N.P., Pastrana L. Production of bacteriocins from Lactococcus lactis subsp. lactis CECT 539 and Pediococcus acidilactici NRRLB-5627 using mussel-processing wastes. Biotechnol. Appl. Biochem. 36:2002;119-125
15. Parente E., Ricciardi A., Addario G. Influence of pH on growth and bacteriocin production by Lactococcus lactis subsp. lactis 140NWC during batch fermentation. Appl. Microbiol. Biotechnol. 41:1994;388-394
16. Parente E., Brienza C., Ricciardi A., Addario G. Growth and bacteriocin production by Enterococcus faecium DPC1146 in batch and continuous culture. J. Ind. Microbiol. Biotechnol. 18:1997;62-67
17. Matsusaki H., Endo N., Sonomoto K., Ishizaki A. Lantobiotic nisin Z fermentative production by Lactococcus lactis IO-1: relationship between production of lantibiotic and lactate and cell growth. Appl. Microbiol. Biotechnol. 45:1996;36-40
18. Chichanoti N., Zaima T., Matsusaki H., Sonomoto K., Ishikazi A. Relationship between nisin Z fermentative production and aeration condition using Lactococcus lactis IO-1. J. Fac. Agric. Kyushu Univ. 43:1997;437-448
19. Guerra N.P., Pastrana L. Influence of pH drop on both nisin and pediocin production by Lactococcus lactis and Pediococcus acidilactici. Lett. Appl. Microbiol. 37:2003;51-55
20. Biswas S.R., Ray P., Johnson M.C., Ray B. Influence of growth conditions on the production of a bacteriocin, pediocin AcH, by Pediococcus acidilactici H. Appl. Environ. Microbiol. 57:1991;1265-1267
21. Yang R., Ray B. Factors influencing production of bacteriocins by lactic acid bacteria. Food Microbiol. 11:1994;281-291
22. Yang R., Johnson M.C., Ray B. Novel method to extract large amounts of bacteriocins from lactic acid bacteria. Appl. Environ. Microbiol. 58:1992;3355-3359
23. Ennahar S., Aoude-Werner D., Sorokine O., Van Dorsselaer A., Bringel F., Hubert J.-C., et al. Production of pediocin AcH by Lactobacillus plantarum WHE92 isolated from cheese. Appl. Environ. Microbiol. 64:1996;3275-3281
24. Guerra N.P., Pastrana L. Enhancement of nisin production by Lactococcus lactis in periodically re-alkalized cultures. Biotechnol. Appl. Biochem. 38:2003;157-167
25. Paik H.D., Glatz B.A. Enhanced bacteriocin production by Propionibacterium thoenii in fed-batch fermentation. J. Food Prot. 60:1997;1529-1533
26. Callewaert R., De Vuyst L. Bacteriocin production with Lactobacillus amylovorus DCE 471 is improved and stabilized by fed-batch fermentation. Appl. Environ. Microbiol. 66:2000;606-613
27. De Vuyst L, Vandamme EJ. Microbial manipulation of nisin biosynthesis and fermentation. In: Jung G, Sahl HG, editors. Nisin novel lantibiotics. Leiden, The Netherlands: ESCOM Science Publishers BV; 1991. p. 397-409.
28. Luedeking R., Piret E.L. Transient and steady states in continuous fermentation. Theory and experiment. J. Biochem. Microbiol. Technol. Eng. 1:1959;431-459
29. a.P., Pastoriza L. A method for bacteriocin quantification. J. Appl. Microbiol. 87:1999;907-914
30. Van Niel E.W.J., Hahn-Hägerdal B. Nutrient requirements of lactococci in defined growth media. Appl. Microbiol. Biotechnol. 52:1999;617-627
31. Nes I.F., Diep D.B., Havarstein L.S., Brurberg M.B., Eijsink V., Holo H. Biosynthesis of bacteriocins in lactic acid bacteria. Anton. Leeuw. Int. J. G. 70:1996;113-128
32. Kim W.S., Hall R.J., Dunn N.W. The effect of nisin concentration and nutrient depletion on nisin production of Lactococcus lactis. Appl. Microbiol. Biotechnol. 48:1997;449-453
33. De Vuyst L., Vandamme E.J. Influence of the phosphorus and nitrogen source on nisin production in Lactococcus lactis subsp. lactis batch fermentations using a complex medium. Appl. Microbiol. Biotechnol. 40:1993;17-22
34. Reiter B., Oram J.D. Nutritional studies on cheese starters. J. Dairy Res. 29:1962;63-77
35. Law B.A., Sezgin E., Sharpe M.E. Amino acid nutrition of some commercial cheese starters in relation to their growth in peptone-supplemented whey media. J. Dairy Res. 43:1976;291-300
36. Guerra N.P., Pastrana L. Nisin and pediocin production on a mussel processing waste supplemented with glucose and five nitrogen sources. Lett. Appl. Microbiol. 34:2002;114-118
37. De Vuyst L. Nutritional factors affecting nisin production by Lactococcus lactis subsp. lactis NIZO 22186 in a synthetic medium. J. Appl. Bacteriol. 78:1995;28-33
38. a.I., Pastrana L., Mirón J. Characterization of microbial biomasses and amylolytic preparations obtained from mussel-processing waste treatment. Biores. Technol. 43:1993;117-125
39. Yamada T., Carlsson J. Regulation of lactate dehydrogenase and change of fermentation products in streptococci. J. Bacteriol. 124:1975;55-61
40. + ratio. J. Bacteriol. 179:1997;5282-5287
41. aP, Pastrana L. Mussel processing wastes as a fermentation substrate. In: Martin AM, editor. Fisheries processing: biotechnological applications. London: Chapman and Hall; 1994. p. 311-43.
42. Cocaign-Bousquet M., Garrigues C., Lubiere P., Lindley N. Physiology of pyruvate metabolism in Lactococcus lactis. Antonie van Leeuw. 70:1996;253-267
43. Blanch HW, Clark DS. Biochemical engineering. USA: Marcel Dekker; 1996.
44. Lejeune R., Callewaert R., Crabbé K., De Vuyst L. Modelling the growth and bacteriocin production by Lactobacillus amylovorus DCE 471 in batch cultivation. J. Appl. Bacteriol. 84:1998;159-168
45. Leroy F., De Vuyst L. Temperature and pH conditions that prevail during fermentation sausages are optimal for production of the antilisterial bacteriocin sakacin K. Appl. Environ. Microbiol. 65:1999;974-981
46. Bibal B., Goma G., Vayssier Y., Pareilleux A. Influence of pH, lactose and lactic acid on the growth of Streptococcus cremoris: a kinetic study. Appl. Microbiol. Biotechnol. 28:1989;340-344
47. Wijtzes T., De Wit J.C., Huis in't Veld J.H.J., van't Riet K., Zwietering M.H. Modelling bacterial growth of Lactobacillus curvatus as a function of acidity and temperature. Appl. Environ. Microbiol. 61:1995;2533-2539
48. Presser K.A., Ratkowsky D.A., Ross T. Modelling the growth rate of Escherichia coli as a function of pH and lactic acid concentration. Appl. Environ. Microbiol. 63:1997;2355-2360
49. Åkerberg C., Hofvendahl K., Zacchi G., Hahn-Hägerdal B. Modelling the influence of pH, temperature, glucose and lactic acid concentrations on the kinetics of lactic acid production by Lactococcus lactis ssp. lactis ATCC 19435 in whole wheat flour. Appl. Microbiol. Biotechnol. 49:1998;682-690
50. Hofvendahl K., van Niel E.W.J., Hahn-Hägerdal B. Effect of temperature and pH on growth and product formation of Lactococcus lactis ssp. lactis ATCC 19435 growing on maltose. Appl. Microbiol. Biotechnol. 51:1999;669-672
51. Poolman B., Konings W.N. Relation of growth of Streptococcus lactis and Streptococcus cremoris to amino acid transport. J. Bacteriol. 170:1988;700-707
52. Gonçalves L.M.D., Ramos A., Almeida J.S., Xavier A.M.R.B., Carrondo M.J.T. Elucidation of the mechanism of lactic acid growth inhibition and production in batch cultures of Lactobacillus rhamnosus. Appl. Microbiol. Biotechnol. 48:1997;346-350
53. Passos F.V., Fleming H.P., Ollis D.F., Felder R.M., McFeeters R.F. Kinetics and modelling of lactic acid production by Lactobacillus plantarum. Appl. Environ. Microbiol. 60:1994;2627-2636
54. Jay J.M. Antimicrobial properties of diacetyl. Appl. Environ. Microbiol. 44:1982;525-532
55. Kadner RJ. Cytoplasmic membrane. In: Neidhardt FC, editor. Escherichia coli and Salmonella: cellular and molecular biology. Washington, DC: American Society for Microbiology; 1996. p. 58-87.
56. Jordan S.L., Glover J., Malcolm L., Thomson-Carter F.M., Booth I.R., Park S.F. Augmentation of killing of Escherichia coli O157 by combinations of lactate, ethanol, and low-pH conditions. Appl. Environ. Microbiol. 65:1999;1308-1311
57. Venkatesh K.V., Okos M.R., Wankat P.C. Kinetic model of growth and lactic acid production from lactose by Lactobacillus bulgaricus. Proc. Biochem. 28:1993;231-241
58. Ahamad M.R., Marth E.H. Behaviour of Listeria monocytogenes at 7, 13, 21, and 35°C in tryptose broth acidified with acetic, citric or lactic acid. J. Food Prot. 52:1989;688-695
59. Besser R.E., Lett S.M., Weber J.T., Doyle M.P., Barrett T.J., Wells J.G., et al. An outbreak of diarrhea and hemolytic uremic syndrome from Escherichia coli o157:H7 in fresh-pressed apple cider. J Am Med Assoc. 269:1993;2217-2220
60. Jay J.M. Do background microorganisms play a role in the safety of fresh food? Trends Food Sci. Technol. 8:1997;421-424