Abstract:Propionic acid (PA) is a valuable organic acid for the food and feed industry, but no bioproduction at industrial scale exists so far. As product inhibition is a major burden for bioprocesses producing organic acids, in situ product removal (ISPR) is desirable. Here, we demonstrate a new strategy to produce PA with a co-culture coupled with ISPR using electrodialysis. Specifically, Bacillus coagulans first produces lactic acid (LA) from sugar(s) and LA is converted to PA using Veillonella criceti. Applying ISP… Show more
“…Moreover, having proven the fermentability of carinata‐derived glucose, metabolites other than those organic acids could also be produced by selecting an appropriate fermentation microorganism. Although CM hydrolysate is a promising feedstock according to the present study, further work is needed to reduce the cost of fermentation through process optimization, including co‐fermenting both glucose and xylose derived (Wei et al, 2016), co‐fermenting biomass hydrolysate and glycerol under high cell density fermentation conditions (Ammar et al, 2020), and incorporating bioprocessing tools (Blanc & Goma, 1987; Jin & Yang, 1998; Selder et al, 2020; Suwannakham & Yang, 2005) and metabolic engineering techniques (Ammar et al, 2014; Guan et al, 2018; Liu et al, 2020; Wang, Ammar, et al, 2015; Wang et al, 2015; Wei et al, 2016).…”
This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
“…Moreover, having proven the fermentability of carinata‐derived glucose, metabolites other than those organic acids could also be produced by selecting an appropriate fermentation microorganism. Although CM hydrolysate is a promising feedstock according to the present study, further work is needed to reduce the cost of fermentation through process optimization, including co‐fermenting both glucose and xylose derived (Wei et al, 2016), co‐fermenting biomass hydrolysate and glycerol under high cell density fermentation conditions (Ammar et al, 2020), and incorporating bioprocessing tools (Blanc & Goma, 1987; Jin & Yang, 1998; Selder et al, 2020; Suwannakham & Yang, 2005) and metabolic engineering techniques (Ammar et al, 2014; Guan et al, 2018; Liu et al, 2020; Wang, Ammar, et al, 2015; Wang et al, 2015; Wei et al, 2016).…”
This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
“…Veillonella criceti as a Gram-negative bacterium can convert lactate to propionate with high productivity rate of 39 g/(L•h) (74). Bacillus coagulans and Lactobacillus zeae are able to convert glucose or other carbon sources to lactate (74,75).…”
Section: Choice Of Microorganismmentioning
confidence: 99%
“…Veillonella criceti as a Gram-negative bacterium can convert lactate to propionate with high productivity rate of 39 g/(L•h) (74). Bacillus coagulans and Lactobacillus zeae are able to convert glucose or other carbon sources to lactate (74,75). The mutant strain of Bacillus coagulans has shown high final titre (145 g/L), yield (0.98 g/g) and d-lactate purity (99.9 %) (76).…”
Section: Choice Of Microorganismmentioning
confidence: 99%
“…The mutant strain of Bacillus coagulans has shown high final titre (145 g/L), yield (0.98 g/g) and d-lactate purity (99.9 %) (76). To avoid product and substrate inhibition, PA (product) and lactate (substrate) should be removed from fermentor and kept at low concentrations (74).…”
Section: Choice Of Microorganismmentioning
confidence: 99%
“…Many different types of carbon sources as the substrate can be considered as the most expensive conventional raw materials in the fermentation process (Table 1 (11,14,23,24,30,58,74,(88)(89)(90)(91)(92)(93)(94)(95)(96)). sources could be proposed as an effective strategy for increasing PA production through kinetics alterations.…”
During the past years, there has been a growing interest in the bioproduction of propionic acid by Propionibacterium. One of the major limitations of the existing models lies in their low productivity yield. Hence, many strategies have been proposed in order to circumvent this obstacle. This article provides a comprehensive synthesis and review of important biotechnological aspects of propionic acid production as a common ingredient in food and biotechnology industries. We first discuss some of the most important production processes, mainly focusing on biological production. Then, we provide a summary of important propionic acid producers, including Propionibacterium freudenreichii and Propionibacterium acidipropionici, as well as a wide range of reported growth/production media. Furthermore, we describe bioprocess variables that can have impact on the production yield. Finally, we propose methods for the extraction and analysis of propionic acid and put forward strategies for overcoming the limitations of competitive microbial production from the economical point of view. Several factors influence the propionic acid concentration and productivity such as culture conditions, type and bioreactor scale; however, the pH value and temperature are the most important ones. Given that there are many reports about propionic acid production from glucose, whey permeate, glycerol, lactic acid, hemicelluloses, hydrolyzed corn meal, lactose, sugarcane molasses and enzymatically hydrolyzed whole wheat flour, only few review articles evaluate biotechnological aspects, i.e. bioprocess variables.
Lactate has various uses as industrial platform chemical, poly-lactic acid precursor or feedstock for anaerobic co-cultivations. The aim of this study was to construct and characterise Acetobacterium woodii strains capable of autotrophic lactate production. Therefore, the lctBCD genes, encoding the native Lct dehydrogenase complex, responsible for lactate consumption, were knocked out. Subsequently, a gene encoding a d-lactate dehydrogenase (LDHD) originating from Leuconostoc mesenteroides was expressed in A. woodii, either under the control of the anhydrotetracycline-inducible promoter Ptet or under the lactose-inducible promoter PbgaL. Moreover, LDHD was N-terminally fused to the oxygen-independent fluorescence-activating and absorption-shifting tag (FAST) and expressed in respective A. woodii strains. Cells that produced the LDHD fusion protein were capable of lactate production of up to 18.8 mM in autotrophic batch experiments using H2 + CO2 as energy and carbon source. Furthermore, cells showed a clear and bright fluorescence during exponential growth, as well as in the stationary phase after induction, mediated by the N-terminal FAST. Flow cytometry at the single-cell level revealed phenotypic heterogeneities for cells expressing the FAST-tagged LDHD fusion protein. This study shows that FAST provides a new reporter tool to quickly analyze gene expression over the course of growth experiments of A. woodii. Consequently, fluorescence-based reporters allow for faster and more targeted optimization of production strains.Key points
•Autotrophic lactate production was achieved with A. woodii.
•FAST functions as fluorescent marker protein in A. woodii.
•Fluorescence measurements on single-cell level revealed population heterogeneity.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.