Analysis of the microbial population dynamics during spontaneous and controlled fermentation of Chili "Charapita" (Capsicum frutescens)

Authors

  • Carlos Vegas Universidad Nacional Mayor de San Marcos, Lima
  • Diego Gonzáles Universidad Nacional Mayor de San Marcos, Lima
  • Salomón Sueros Universidad Nacional Mayor de San Marcos, Lima
  • Abad Hurtado Universidad Nacional Mayor de San Marcos, Lima
  • Amparo I. Zavaleta Universidad Nacional Mayor de San Marcos, Lima

DOI:

https://doi.org/10.17268/sci.agropecu.2016.03.06

Keywords:

spontaneous fermentation, controlled fermentation, Capsicum frutescens, LAB, yeasts

Abstract

Chilies are the main ingredients of the Peruvian gastronomy. Chili "Charapita" (Capsicum frutescens) is very used in amazon food. The last decade, "the gastronomic boom" has increased their demand, so it is necessary to develop new technologies for their preservation sustainably, healthy, without affecting the environment. The aim of the present work was to analyze the microbial population dynamics during Chili "Charapita" fermentation using spontaneous (SF) and controlled (CF) fermentation. Fermentations were conducted at pilot scale and room temperature with chilies from Iquitos city. A lactic acid bacteria (LAB) strain type belonging to Lactobacillus plantarum ATCC 14917 was used in FC. Fermentations were monitored through reducing sugars, acidity and pH determinations. Microbial tests were performed: total cells count by microscopy and microbial growth in culture media. LAB, yeasts, enterobacteriaceae and pseudomonas were recovered in MRS, YPD, McConkey and Cetrimide media, respectively. Both fermentations finalized at 47 days, reducing sugars were below 0.5 g/L and 3.07 3.11 of pH. However, the acidity in SF was higher than CF (1.58% vs. 1.20%). At microbiological level, LAB and yeasts were microorganisms responsible for SF. However, starter LAB was not suitable for CF. In fact, it was replaced by yeasts and enterobacterias. So, the use of autochthonous microorganisms of the fermentation as starter is important for a better fermentation control.

References

Abriouel, H.; Benomar, N.; Lucas, R.; Gálvez, A. 2011. Culture-independent study of the diversity of microbial populations in brines during fermentation of naturally fermented Aloreña green table olives. International Journal of Food Microbiology 144: 487–496.

Arroyo-López, F.; Querol, A.; Bautista-Gallego, J.; Garrido-Fernández, A. 2008. Role of yeasts in table olive production. International Journal of Food Microbiology 128: 189-196.

Baylis, C.; Uyttendaele, M.; Joosten, H.; Davies, A. 2011. The enterobacteriaceae and their significance to the food industry. ILSI Europe Report Series. 17–28.

Cocolin, L.; Alessandria, V.; Dolci, P.; Gorra, R.; Rantsiou, K. 2013. Culture independent methods to assess the diversity and dynamics of microbiota during food fermentation. International Journal of Food Microbiology 167: 29–43.

DeVuyst, L.; Vandamme, E. 1994. Antimicrobial potential of lactic acid bacteria, p. 91–142. In L. DeVuyst and E.J. Vandamme (ed.), Bacteriocins of Lactic acid Bacteria. Blackie Academic and Professional, London, United Kingdom.

DiCagno, R.; Surico, R.F.; Minervini, G.; De Angelis, M.; Rizello, C.G., Gobbetti, M. 2009. Use of autochthonous starters to ferment red and yellow peppers (Capsicum annum L.). International Journal of Food Microbiology 130: 108–116.

Fleming, H. 1982. Fermented vegetables. In A.H. Rose (ed.), Economic microbiology. Fermented foods, vol. 7. Academic Press, New York. 227 pp.

Holmes, D.; Peck, H. 1993. Analytical Biochemistry. Longman Scientific and Technical, London.

Holzapfel, W. 2002. Appropriate starter culture technologies for small- scale fermentation in developing countries. International Journal of Food Microbiology 75: 197–212.

Idoui, T.; Boudjerda, J.; Leghouchi, E.; Karam, N.E. 2009. Naturally fermented Jijelian black olives: microbiological characteristics and isolation of lactic acid bacteria. Grasas y Aceites 60 (5): 514-518.

Kalantzopoulos, G. 1997. Fermented products with probiotic qualities. Anaerobe 3: 185-190.

Miller, G. 1959. Use of Dinitrosalisyc Acid Reagents for determination of reducing sugar. Anal Chem. 31: 426-428.

Mohammed, S.; Steenson, L.; Kirleis, A. 1991. Isolation and characterisation of microorganisms associated with the traditional sorghum fermentation for production of Sudanese Kisra. Applied and Environmental Microbiology 57: 2529-2533.

Nout, M.J.R. 1991. Ecology of accelerated natural lactic fermentation of sorghum-based infant food formulas. International Journal of Food Microbiology 12: 217-224.

Oliver, J. 2005. Viable but nonculturable bacteria in food environments. In: Fratamico, P.M., Bhunia, A.K., Smith, L. (Eds.), Foodborne Pathogens. Microbiology and Molecular biology. Caister Academic Press, UK.

Park, S.; Chang, J.; Cha, S.; Moon, G.; 2009. Analysis of the bacterial composition during Kochujang, a Korean traditional fermented hot pepper-soybean paste, fermentation. Food Science and Biotechnology 18: 1035–1037.

Peres, C.; Catulo, L.; Brito, D.; Pintado, C. 2008. Lactobacillus pentosus DSM 16366 starter added to brine as freeze-dried and as culture in the nutritive media for Spanish style green olive production. Grasas y Aceites 59(3): 234-238.

Pérez, R.; Ben Omar, N.; Abriouel, H.; Lucas, R.; Martínez, M.; Gálvez, A. 2005. Microbiological Study of Lactic Acid Fermentation of Caper Berries by Molecular and Culture-Dependent Methods. Applied and Environmental Microbiology 71 (12): 7872-7879.

Pérez-Díaz, I.; Breidt, F.; Buescher, R.; Arroyo-López, F.; Jiménez-Díaz, R.; Garrido, A.; Bautista, J.; Yoo, S..; Johanningsmeier, S. 2014. Fermented and Acidified Vegetables.F. Pouch Downes, K.A. Ito (Eds.), Compendium of Methods for the Microbiological Examination of Foods (5th ed.), American Public Health Association (Chapter 51).

Psani, M.; Kotzekidou, P. 2006. Technological characteristics of yeast strains and their potential as starter adjuncts in Greek-style black olive fermentation. World Journal of Microbiology and Biotechnology 22: 1329–1336.

Pundir, R.; Jain, P. 2010. Change in microflora of sauerkraut during fermentation and storage. World Journal of Dairy and Food Science 5: 221-225.

Torija, M.J.; Rozes, N.; Poblet, M.; Guillamón, J.M.; Mas, A. 2001. Yeast population dynamics in spontaneous fermentations: comparison between two different wine areas during three consecutive years. Antonie van Leeuwenhoek 79: 345 – 352.

Vegas, C.; Mateo, E.; González, A.; Jara, C.; Guillamón, J.; Poblet, M.; Torija, M.; Mas, A. 2010. Population dynamics of acetic acid bacteria during traditional wine vinegar production. International Journal of Food Microbiology 138: 130–136.

Received May 02, 2016.

Accepted June 21, 2016.

* Corresponding author

E-mail: carlosvegas@hotmail.com (C. Vegas).

Published

2016-09-13

How to Cite

Vegas, C., Gonzáles, D., Sueros, S., Hurtado, A., & Zavaleta, A. I. (2016). Analysis of the microbial population dynamics during spontaneous and controlled fermentation of Chili "Charapita" (Capsicum frutescens). Scientia Agropecuaria, 7, 201-206. https://doi.org/10.17268/sci.agropecu.2016.03.06

Issue

Section

Original Articles