Abstract

Background1,3-propanediol (1,3-PDO) is the most widely studied value-added product that can be produced by feeding glycerol to bacteria, including Lactobacillus sp. However, previous research reported that L. reuteri only produced small amounts and had low productivity of 1,3-PDO. It is urgent to develop procedures that improve the production and productivity of 1,3-PDO.ResultsWe identified a novel L. reuteri CH53 isolate that efficiently converted glycerol into 1,3-PDO, and performed batch co-fermentation with glycerol and glucose to evaluate its production of 1,3-PDO and other products. We optimized the fermentation conditions and nitrogen sources to increase the productivity. Fed-batch fermentation using corn steep liquor (CSL) as a replacement for beef extract led to 1,3-PDO production (68.32 ± 0.84 g/L) and productivity (1.27 ± 0.02 g/L/h) at optimized conditions (unaerated and 100 rpm). When CSL was used as an alternative nitrogen source, the activity of the vitamin B12-dependent glycerol dehydratase (dhaB) and 1,3-propanediol oxidoreductase (dhaT) increased. Also, the productivity and yield of 1,3-PDO increased as well. These results showed the highest productivity in Lactobacillus species. In addition, hurdle to 1,3-PDO production in this strain were identified via analysis of the half-maximal inhibitory concentration for growth (IC50) of numerous substrates and metabolites.ConclusionsWe used CSL as a low-cost nitrogen source to replace beef extract for 1,3-PDO production in L. reuteri CH53. These cells efficiently utilized crude glycerol and CSL to produce 1,3-PDO. This strain has great promise for the production of 1,3-PDO because it is generally recognized as safe (GRAS) and non-pathogenic. Also, this strain has high productivity and high conversion yield.

Highlights

  • The results indicated that L. reuteri CH53 grouped with other strains in the genus Lactobacillus, and most closely with L. reuteri JCM1112

  • Pflügl et al [17], reported vitamin B12 addition significantly enhanced the production of 1,3-PDO by Lactobacillus diolivorans and Wischral et al [40] reported enhanced production of 1,3-PDO by Clostridium beijerinckii when corn steep liquor (CSL) was used as a nitrogen source. These results suggest that CSL can be used as an effective and low-cost nitrogen source for 1,3-PDO production by L. reuteri CH53, and is a suitable replacement for beef extract

  • We optimized the culture of a new isolate, L. reuteri CH53, and improved the efficiency of 1,3-PDO production using crude glycerol and CSL as substrates

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Summary

Objectives

The aim of the present study is to examine the effect of various operational strategies on the production and productivity of 1,3-PDO using the newly isolated L. reuteri CH53

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Results
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