| Literature DB >> 33824622 |
Duygu Alp1, Özcan Bulantekin1.
Abstract
With the drying process, the water activity and moisture content of the foods are reduced, so the growth of microorganisms in the foods is largely prevented/postponed. But low-aw foods should not be considered sterile they can be contaminated by fungi and other contaminants during the drying process under unhygienic conditions. If drying is not done to a sufficient degree of moisture during food processing and storage, where dried foods are processed, sometimes the minimum value is reached for the growth of microorganisms. In dry foods, some pathogens, yeast and molds can continue to grow during storage, transport and transportation until the sale and they causing spoilage. They can even cause health problems if enough pathogen or spore cells remain viable. Considering this situation today, it is attempted to obtain high-quality dried foods with good microbiologically and chemically properties. For this purpose, various drying methods have been developed. Most studies suggest that when foods are pre-treated with the ascorbic acid or sodium metabisulfite or applied with various combined methods such as UV irradiation, supercritical carbon dioxide (SCO2), low-pressure superheated steam drying (LPSSD), and infrared (IR) drying, they can be effective on inactivation of microorganisms. We have reviewed in this study how these methods made dried products efficient of microbial inactivation and microbiologically safe.Entities:
Keywords: Bacterial survivor; Dried fruits and vegetables; Drying methods; Emerging technologies in food processing; Food safety; Microbial inactivation
Year: 2021 PMID: 33824622 PMCID: PMC8017434 DOI: 10.1007/s00217-021-03731-z
Source DB: PubMed Journal: Eur Food Res Technol ISSN: 1438-2377 Impact factor: 2.998
The results of microorganisms inactivation by the studies using different drying methods
| Drying method | Microorganisms | Food | Conditions | Effect/approximate reduction log (cfu/g) | References |
|---|---|---|---|---|---|
| Convective air drying | Peach slices | 6 h at 60 °C | 5.30 | DiPersio et al. (2004) | |
| Convective air drying | Apple slices | 6 h at 62 °C | 3.50 | Burnham et al. (2001) | |
| Microwave freeze drying | Mesophilic bacteria | Cabbage slices | 6 h at 100 Pa 700 W | 0.90 | Duan et al. (2007) |
| Freeze drying | Mesophilic bacteria | Cabbage slices | 15 h at 100 Pa | Almost no reduction | Duan et al. (2007) |
| Convective air drying | Cabbage slices | 3 h at 60 °C | 4.50 | Chiewchan and Morakotjinda (2009) | |
| Convective air drying | Cabbage | 2.5 h at 50–70 °C | 4.50 | Haware et al. (2009) | |
| Convective air drying | Cabbage slices | 4 h at 70 °C | 6.30 | Phungamngoen et al. (2011) | |
| Vacuum drying | Cabbage slices | 1.5 h at 70 °C 10 kPa | 3.30 | Phungamngoen et al. (2011) | |
| LPSSD drying | Cabbage slices | 1.75 h at 70 °C 10 kPa | 6.70 | Phungamngoen et al. (2011) | |
| Convective air drying | Carrot slices | 6 h at 60 °C | 1.65 cfu/g | DiPersio et al. (2007) | |
| Microwave vacuum drying | Total aerobic count, yeasts and molds | Carrot slices | 58 min 15 kPa 1800 W | 1.7 and 1.5–2.2 | Yaghmaee and Durance, (2007) |
| Microwave + microwave vacuum drying | Total aerobic count, yeasts and molds | Carrot slices | 12 then 46 min 15 kPa 1800 W | 4.0 and 1.3–3.9 | Yaghmaee and Durance, (2007) |
| Catalytic infrared drying | Mesophilic bacteria | Onion | 40 min at 80 °C | 1.7 | Gabel et al. (2006) |
| Conventional drying | Tarhana | 36 h at 55 °C | 2.0 | Dağlıoğlu et al. (2002) | |
| Microwave drying | Tarhana | 36 h 1500 W | 4.0 | Dağlıoğlu et al. (2002) | |
| Convective air drying | Apple slices | 6 h at 62.8 °C | 3.0 | Derrickson-Tharrington et al. (2005) | |
| Acid treatment + convective air drying + | Apple slices | 6 h at 62.8 °C | 6.0 | Derrickson-Tharrington et al. (2005) | |
| Acid treatment + convective air drying + | Apple slices | 6 h at 60 °C | 4.3 and 5.2 | DiPersio et al. (2003) | |
| Supercritical carbon dioxide (scCO2) | Yeasts, molds and Mesophilic bacteria | Herbs | 0-150 min 10 MPa at 40–50 °C | 2.0 and 4.0 | Zambon et al. (2018) |
| Ozone gas | Yeasts, molds and | Figs | 13.8 and 1.7 mg L−1 | Complete inactivation | Zorlugenç et al. (2008) |
| Ozonated water | Yeasts, molds and | Figs | 7.5, 15, 30 min | 0.16–1.57–2.09 | Zorlugenç et al. (2008) |
| Ozonation | Figs | 0.1, 0.5, 1.0 ppm 36 min at 20 °C, 70% relative humidity | 1.0–2.0–3.5 | Akbaş and Özdemir (2008) | |
| Ozonation | Figs | 0.1, 0.5, 1.0 ppm 36 min at 20 °C, 70% relative humidity | 2.0–3.0–3.5 | Akbaş and Özdemir (2008) | |
| Ozonation | Figs | 1.0,5.0,7.0and 9.0 ppm 36 min at 20 °C, 70% relative humidity | 0.5–1.0–1.5–2.0 | Akbaş and Özdemir (2008) |