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High throughput automated colorimetric method for the screening of l-lactic acid producing microorganisms
Author(s) -
Nadège Liaud,
David Navarro,
Nicolas Vidal,
JeanClaude Sigoillot,
Sana Raouche
Publication year - 2014
Publication title -
methodsx
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.356
H-Index - 23
ISSN - 2215-0161
DOI - 10.1016/j.mex.2014.10.001
Subject(s) - lactic acid , high throughput screening , abts , chemistry , chromogenic , substrate (aquarium) , chromatography , biochemistry , bacteria , biology , antioxidant , ecology , genetics , dpph
Lactic acid is a valuable and fully degradable organic acid with promising applications in poly-lactic acid production (Taskila S and Ojamo, 2013 [1]). Despite their efficiency, the cost of the current lactic acid bio-processes is still an obstacle to this application (Miller et al., 2011 [2]). To ameliorate lactic acid producing strains, researchers are using mutations and metabolic engineering techniques, as well as medium optimization. All these studies necessitate a good and high throughput screening method. Currently, researchers mostly use HPLC methods which often necessitate sample preparation, are not stereospecific and do not allow high throughput. To help optimizing l-lactic acid production, we developed a high throughput colorimetric method inspired by the blood l-lactic acid detection method used for diagnosis (Lin et al., 1999 [3]).•Two sequential enzymatic reactions using l-lactate oxidase, peroxidase and ABTS (2,2'-azino-di-[3-ethylbenzthiazoine-sulfonate]), a chromogenic peroxidase substrate, are used to quantify l-lactate between 13.8 and 90 mg/l.•The accuracy of the method was ascertained before automation.•The method was successfully applied for the direct determination of l-lactate content in fungal culture supernatants.

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