Biochemical butyrate production via dark fermentation as an energetically efficient alternative management approach for vinasse in sugarcane biorefineries

2020 ◽  
Vol 158 ◽  
pp. 3-12 ◽  
Author(s):  
Lucas Tadeu Fuess ◽  
Graciete Mary dos Santos ◽  
Tiago Palladino Delforno ◽  
Bruna de Souza Moraes ◽  
Ariovaldo José da Silva
2011 ◽  
Vol 1 (1) ◽  
pp. 55-63 ◽  
Author(s):  
Eng H. Ooi ◽  
Jordan T. Glicksman ◽  
Allan D. Vescan ◽  
Ian J. Witterick

Marine Policy ◽  
2007 ◽  
Vol 31 (4) ◽  
pp. 505-516 ◽  
Author(s):  
Robert J. Johnston ◽  
Daniel S. Holland ◽  
Vishwanie Maharaj ◽  
Tammy Warner Campson

2014 ◽  
Vol 113 (7) ◽  
pp. S142
Author(s):  
Mehmet Emin Kalkan ◽  
Mustafa Akçakoyun ◽  
Serdar Demir ◽  
Elnur Alizade ◽  
Göksel Açar ◽  
...  

Author(s):  
Anna Detman ◽  
Daniel Laubitz ◽  
Aleksandra Chojnacka ◽  
Pawel R. Kiela ◽  
Agnieszka Salamon ◽  
...  

Abstract Background: This study focuses on the processes occurring during acidogenic step of anaerobic digestion, especially resulting from nutritional interactions between dark fermentation (DF) bacteria and lactic acid bacteria (LAB). Previously, we have confirmed that DF microbial communities fed on molasses are able to convert lactate and acetate to butyrate in batch experiments. The aims of the study were: (i) to recognize biodiversity of DF microbial communities able and unable to convert lactate and acetate to butyrate and (ii) to define the conditions for the transformation in static batch experiments.Results: Sucrose stimulated bacterial growth, especially LAB. In the samples where the microbial communities fermented media containing carbohydrates the two main tendencies were observed: (i) a low pH (pH≤4), lactate and ethanol as the main fermentation products, microbial communities dominated with Lactobacillus, Bifidobacterium, Leuconostoc and Fructobacillus was characterised by a low biodiversity; (ii) pH in the range 5.0-6.0, butyrate dominated among the fermentation products, the microbial communities composed mailny of Clostridium (especially Clostridium sensu stricto 12), Lactobacillus, Bifidobacterium and Prevotella. The biodiversity increased with the ability to convert acetate and lactate to butyrate. The microbial communities processing exclusively lactate and acetate showed the highest biodiversity and was dominated by Clostridium (especially Clostridium sensu stricto 12). LAB were reduced, other genera such as Terrisporobacter, Lachnoclostridium, Paraclostridium or Sutterella were found. Butyrate was the main metabolite and pH was 7. WGS analysis of the selected butyrate-producing microbial communities independently on the substrate, revealed C. tyrobutyricum as a dominant Clostridium species. Conclusions: The batch tests revealed dynamics of metabolic activity and composition of DF microbial communities dependent on fermentation conditions. The results expand our knowledge on lactate to butyrate conversion by DF microbial communities. The relevant factor for conversion of lactate and acetate to butyrate in the presence of carbohydrates is pH in the range 5-6 and the balance between LAB (especially Lactobacillus), lactate and acetate producers (Bifidobacterium) and butyrate producers (mainly Clostridium) as well Prevotella. The pH below 4 and ethanol concentration might be the signalling factors responsible for metabolic shift of the dark fermentation microbial communities towards lactate fermentation.


2020 ◽  
Author(s):  
Juan Cubero-Cardoso ◽  
Antonio Serrano ◽  
Ángeles Trujillo-Reyes ◽  
Denys K. Villa-Gómez ◽  
Rafael Borja ◽  
...  

This review summarizes and critically analyzes the different types of potential valorization options for strawberry extrudate in order to have a broader overview of the potential management of this waste. Animal feed is commonly used as a management option for the strawberry extrudate; however, most of the strawberry extrudate is disposed in landfills. Strawberry extrudate contains different bioactive compounds that encourage the use of an alternative management approach than landfilled. The present review offers a complete comparative, including the advantages and drawbacks of each reviewed technique, to facilitate the selection of the most suitable technology for the different valorization scenarios. This review has been structured in three sections: 1. Composition of the strawberry extrudate and strawberry especially focused on their content in bioactive compounds. 2. The different techniques of extraction and purification of bioactive compounds. 3. The handling and management of the resulting biomass after the extraction process of bioactive compounds.


2022 ◽  
pp. 100940
Author(s):  
Thiago Ravanini do Nascimento ◽  
Willame Araujo Cavalcante ◽  
Guilherme Henrique Duarte de Oliveira ◽  
Marcelo Zaiat ◽  
Rogers Ribeiro

Microbiome ◽  
2021 ◽  
Vol 9 (1) ◽  
Author(s):  
Anna Detman ◽  
Daniel Laubitz ◽  
Aleksandra Chojnacka ◽  
Pawel R. Kiela ◽  
Agnieszka Salamon ◽  
...  

Abstract Background This study focuses on the processes occurring during the acidogenic step of anaerobic digestion, especially resulting from nutritional interactions between dark fermentation (DF) bacteria and lactic acid bacteria (LAB). Previously, we have confirmed that DF microbial communities (MCs) that fed on molasses are able to convert lactate and acetate to butyrate. The aims of the study were to recognize the biodiversity of DF-MCs able and unable to convert lactate and acetate to butyrate and to define the conditions for the transformation. Results MCs sampled from a DF bioreactor were grown anaerobically in mesophilic conditions on different media containing molasses or sucrose and/or lactate and acetate in five independent static batch experiments. The taxonomic composition (based on 16S_rRNA profiling) of each experimental MC was analysed in reference to its metabolites and pH of the digestive liquids. In the samples where the fermented media contained carbohydrates, the two main tendencies were observed: (i) a low pH (pH ≤ 4), lactate and ethanol as the main fermentation products, MCs dominated with Lactobacillus, Bifidobacterium, Leuconostoc and Fructobacillus was characterized by low biodiversity; (ii) pH in the range 5.0–6.0, butyrate dominated among the fermentation products, the MCs composed mainly of Clostridium (especially Clostridium_sensu_stricto_12), Lactobacillus, Bifidobacterium and Prevotella. The biodiversity increased with the ability to convert acetate and lactate to butyrate. The MC processing exclusively lactate and acetate showed the highest biodiversity and was dominated by Clostridium (especially Clostridium_sensu_stricto_12). LAB were reduced; other genera such as Terrisporobacter, Lachnoclostridium, Paraclostridium or Sutterella were found. Butyrate was the main metabolite and pH was 7. Shotgun metagenomic analysis of the selected butyrate-producing MCs independently on the substrate revealed C.tyrobutyricum as the dominant Clostridium species. Functional analysis confirmed the presence of genes encoding key enzymes of the fermentation routes. Conclusions Batch tests revealed the dynamics of metabolic activity and composition of DF-MCs dependent on fermentation conditions. The balance between LAB and the butyrate producers and the pH values were shown to be the most relevant for the process of lactate and acetate conversion to butyrate. To close the knowledge gaps is to find signalling factors responsible for the metabolic shift of the DF-MCs towards lactate fermentation.


Author(s):  
Etienne de Harven ◽  
Nina Lampen

Samples of heparinized blood, or bone marrow aspirates, or cell suspensions prepared from biopsied tissues (nodes, spleen, etc. ) are routinely prepared, after Ficoll-Hypaque concentration of the mononuclear leucocytes, for scanning electron microscopy. One drop of the cell suspension is placed in a moist chamber on a poly-l-lysine pretreated plastic coverslip (Mazia et al., J. Cell Biol. 66:198-199, 1975) and fifteen minutes allowed for cell attachment. Fixation, started in 2. 5% glutaraldehyde in culture medium at room temperature for 30 minutes, is continued in the same fixative at 4°C overnight or longer. Ethanol dehydration is immediately followed by drying at the critical point of CO2 or of Freon 13. An efficient alternative method for ethanol dehydrated cells is to dry the cells at low temperature (-75°C) under vacuum (10-2 Torr) for 30 minutes in an Edwards-Pearse freeze-dryer (de Harven et al., SEM/IITRI/1977, 519-524). This is preceded by fast quenching in supercooled ethanol (between -90 and -100°C).


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