4.7 Article

Food waste to new food: Risk assessment and microbial community analysis of anaerobic digestate as a nutrient source in hydroponic production of vegetables

期刊

JOURNAL OF CLEANER PRODUCTION
卷 333, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.jclepro.2021.130239

关键词

Circular food production systems; Food-borne pathogens; Isothermal calorimetry; Microbial community analysis; Microbial food safety risk assessment; Waste recovery

资金

  1. Swedish Research Council for Environment, Agricultural Sciences and Spatial Planning (FORMAS) [2018-01845]
  2. Formas [2018-01845] Funding Source: Formas

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This study evaluated the microbiological food safety of using anaerobic digestate as a fertilizer in hydroponic production of vegetables. The results showed that the biofertilizer based on anaerobic digestate is considered microbiologically safe for use in hydroponic cultivation, but continuous risk assessment is important.
In this study, the microbiological food safety of using anaerobic digestate as a fertilizer in hydroponic production of vegetables was evaluated. The used anaerobic digestate was a liquid residue obtained from the digestion of food waste in the production of biogas. Replacing the customary inorganic fertilizer used in hydroponic pro-duction with this recycled fertilizer (biofertilizer) could allow for sustainable urban food production close to retailers and consumers. However, in striving for circular food production, it is vital that the food safety of utilizing recycled resources is ensured. Especially in the application of hydroponic farming, where the nutrient loop is shorter than on arable land, a microbiological food safety risk assessment is crucial when adopting new and recycled fertilizers. The biofertilizer based on anaerobic digestate was therefore studied with regard to its microbial community (16S rRNA gene amplicon sequencing) during production of vegetables in a hydroponic system. The biofertilizer was also challenge tested with food borne pathogens (Salmonella enterica, Listeria monocytogenes and Bacillus cereus). Furthermore, the microbial activity of the biofertilizer was studied using isothermal calorimetry. The results showed that the microbial community of the biofertilizer changed distinctly through a necessary initial nitrification process, and that the most abundant genus was Mycobacterium. Deliberate contaminations with 5 log(10) CFU mL(-1) of either S. enterica or L. monocytogenes in the nitrified biofertilizer were no longer detectable with selective plating after 48 h of incubation at 20 degrees C. Selective plating for B. cereus revealed that the biofertilizer contained low levels (similar to 10 CFU mL(-1)) of the bacterium, and an inoculation of 5 log(10) CFU mL(-1) B. cereus decreased to these levels within 24 h of incubation at 20 degrees C. Analysis of the microbial activity of the biofertilizer indicated that the biofertilizer does not seem to support microbial activity without the addition of an external nutrient source that contains an accessible carbon source and trace elements. The type of biofertilizer investigated in this study is thus regarded as microbiologically safe for use in hydroponic cultivation. The constant presence of viable B. cereus, however, emphasizes the fundamental importance of continuous risk assessment in case of any modifications or supplementations of the biofertilizer, since it clearly can act as a reservoir for bacterial endospores.

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