scholarly journals Modeling dark fermentation of cheese whey for H2 and n-butyrate production considering the chain elongation perspective

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

2022 ◽  
Vol 304 ◽  
pp. 114253
Author(s):  
Jaqueline Cardoso Ribeiro ◽  
Vera Tainá Mota ◽  
Valéria Maia de Oliveira ◽  
Marcelo Zaiat

Author(s):  
Giovanna Lovato ◽  
Isabela Mehi Gaspari Augusto ◽  
Antônio Djalma Nunes Ferraz Júnior ◽  
Roberta Albanez ◽  
Suzana Maria Ratusznei ◽  
...  

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.


Author(s):  
Flávio C. F. Baleeiro ◽  
Magda S. Ardila ◽  
Sabine Kleinsteuber ◽  
Heike Sträuber

Mixed microbial cultures have become a preferred choice of biocatalyst for chain elongation systems due to their ability to convert complex substrates into medium-chain carboxylates. However, the complexity of the effects of process parameters on the microbial metabolic networks is a drawback that makes the task of optimizing product selectivity challenging. Here, we studied the effects of small air contaminations on the microbial community dynamics and the product formation in anaerobic bioreactors fed with lactate, acetate and H2/CO2. Two stirred tank reactors and two bubble column reactors were operated with H2/CO2 gas recirculation for 139 and 116 days, respectively, at pH 6.0 and 32°C with a hydraulic retention time of 14 days. One reactor of each type had periods with air contamination (between 97 ± 28 and 474 ± 33 mL O2 L−1 d−1, lasting from 4 to 32 days), while the control reactors were kept anoxic. During air contamination, production of n-caproate and CH4 was strongly inhibited, whereas no clear effect on n-butyrate production was observed. In a period with detectable O2 concentrations that went up to 18%, facultative anaerobes of the genus Rummeliibacillus became predominant and only n-butyrate was produced. However, at low air contamination rates and with O2 below the detection level, Coriobacteriia and Actinobacteria gained a competitive advantage over Clostridia and Methanobacteria, and propionate production rates increased to 0.8–1.8 mmol L−1 d−1 depending on the reactor (control reactors 0.1–0.8 mmol L−1 d−1). Moreover, i-butyrate production was observed, but only when Methanobacteria abundances were low and, consequently, H2 availability was high. After air contamination stopped completely, production of n-caproate and CH4 recovered, with n-caproate production rates of 1.4–1.8 mmol L−1 d−1 (control 0.7–2.1 mmol L−1 d−1). The results underline the importance of keeping strictly anaerobic conditions in fermenters when consistent n-caproate production is the goal. Beyond that, micro-aeration should be further tested as a controllable process parameter to shape the reactor microbiome. When odd-chain carboxylates are desired, further studies can develop strategies for their targeted production by applying micro-aerobic conditions.


Processes ◽  
2021 ◽  
Vol 9 (6) ◽  
pp. 1017
Author(s):  
Margarita Andreas Dareioti ◽  
Aikaterini Ioannis Vavouraki ◽  
Konstantina Tsigkou ◽  
Constantina Zafiri ◽  
Michael Kornaros

The aim of this study was to determine the optimal conditions for dark fermentation using agro-industrial liquid wastewaters mixed with sweet sorghum stalks (i.e., 55% sorghum, 40% cheese whey, and 5% liquid cow manure). Batch experiments were performed to investigate the effect of controlled pH (5.0, 5.5, 6.0, 6.5) on the production of bio-hydrogen and volatile fatty acids. According to the obtained results, the maximum hydrogen yield of 0.52 mol H2/mol eq. glucose was measured at pH 5.5 accompanied by the highest volatile fatty acids production, whereas similar hydrogen productivity was also observed at pH 6.0 and 6.5. The use of heat-treated anaerobic sludge as inoculum had a positive impact on bio-hydrogen production, exhibiting an increased yield of 1.09 mol H2/mol eq. glucose. On the other hand, the pretreated (ensiled) sorghum, instead of a fresh one, led to a lower hydrogen production, while the organic load decrease did not affect the process performance. In all experiments, the main fermentation end-products were volatile fatty acids (i.e., acetic, propionic, butyric), ethanol and lactic acid.


Author(s):  
Bin Liu ◽  
Denny Popp ◽  
Heike Sträuber ◽  
Hauke Harms ◽  
Sabine Kleinsteuber

Abstract Background The platform chemicals n-caproate and iso-butyrate can be produced by anaerobic fermentation from agro-industrial residues in a process known as microbial chain elongation. A few chain-elongating species have been discovered to utilize lactate and used to study the physiology of lactate-based chain elongation in pure cultures. Recently we isolated three novel clostridial species (strains BL-3, BL-4 and BL-6) that convert lactate to n-caproate and iso-butyrate. Here, we analyzed the genetic background of lactate-based chain elongation in these strains and other chain-elongating species by comparative genomics. Results All three strains produced n-caproate and iso-butyrate from lactate, with the highest proportions of n-caproate (18%) for BL-6 and iso-butyrate (23%) for BL-4 in batch cultivation at pH 5.5. The strains are suggested to represent three novel species based on low similarities with their closest described relatives. The three genomes show low conservation of organization and a relatively small core-genome size (504 out of 6,654 gene families). Including data of another eleven experimentally validated chain-elongating strains, we found that the chain elongation-specific core-genome harbors genes involved in reverse β-oxidation, hydrogen formation and energy conservation, displaying substantial genome heterogeneity. The three new isolates contain the genes for lactate oxidation and a gene cluster encoding enzymes of reverse β-oxidation, including the CoA transferase for the formation of n-caproate. Our analysis gave no hints on the isomerization pathway for iso-butyrate formation. An operon encoding the Rnf complex was found in BL-3 and BL-4 but not in BL-6, which may instead use the Ech hydrogenase complex for energy conservation. BL-3 and BL-6 were predicted to have genes encoding both the BCD/EtfAB complex and the LDH/EtfAB complex for energy coupling. Conclusions The genetic background of lactate-based chain elongation was confirmed in three novel Clostridia species that convert lactate to n-caproate and iso-butyrate. They contain highly conserved genes involved in reverse β-oxidation, hydrogen formation and either of two types of energy conservation systems (Rnf and Ech). Further research is needed to elucidate the mechanism of iso-butyrate formation in these strains. Features of the three isolates may be interesting for further applications in n-caproate and iso-butyrate production.


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