Improved intracellular PHA determinations with novel spectrophotometric quantification methodologies based on Sudan black dye

The presence of intracellular polyhydroxyalkanoates (PHAs) is usually studied using Sudan black dye solution (SB). In a previous work it was shown that the PHA could be directly quantified using the absorbance of SB fixed by PHA granules in wet cell samples. In the present paper, the optimum SB amou...

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Veröffentlicht in:Journal of microbiological methods 2018-05, Vol.148, p.1-11
Hauptverfasser: Porras, Mauricio A., Villar, Marcelo A., Cubitto, María A.
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Villar, Marcelo A.
Cubitto, María A.
description The presence of intracellular polyhydroxyalkanoates (PHAs) is usually studied using Sudan black dye solution (SB). In a previous work it was shown that the PHA could be directly quantified using the absorbance of SB fixed by PHA granules in wet cell samples. In the present paper, the optimum SB amount and the optimum conditions to be used for SB assays were determined following an experimental design by hybrid response surface methodology and desirability-function. In addition, a new methodology was developed in which it is shown that the amount of SB fixed by PHA granules can also be determined indirectly through the absorbance of the supernatant obtained from the stained cell samples. This alternative methodology allows a faster determination of the PHA content (involving 23 and 42 min for indirect and direct determinations, respectively), and can be undertaken by means of basic laboratory equipment and reagents. The correlation between PHA content in wet cell samples and the spectra of the SB stained supernatant was determined by means of multivariate and linear regression analysis. The best calibration adjustment (R2 = 0.91, RSE: 1.56%), and the good PHA prediction obtained (RSE = 1.81%), shows that the proposed methodology constitutes a reasonably precise way for PHA content determination. Thus, this methodology could anticipate the probable results of the above mentioned direct PHA determination. Compared with the most used techniques described in the scientific literature, the combined implementation of these two methodologies seems to be one of the most economical and environmentally friendly, suitable for rapid monitoring of the intracellular PHA content. •Optimization process for Sudan black methodology for direct PHA quantification•Development of a methodology for the indirect determination of PHA content•Fast, simple, cheap and environmentally friendly methodologies that use basic equipment.•Combined methodologies can be implemented in parallel and at a very low cost.
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In a previous work it was shown that the PHA could be directly quantified using the absorbance of SB fixed by PHA granules in wet cell samples. In the present paper, the optimum SB amount and the optimum conditions to be used for SB assays were determined following an experimental design by hybrid response surface methodology and desirability-function. In addition, a new methodology was developed in which it is shown that the amount of SB fixed by PHA granules can also be determined indirectly through the absorbance of the supernatant obtained from the stained cell samples. This alternative methodology allows a faster determination of the PHA content (involving 23 and 42 min for indirect and direct determinations, respectively), and can be undertaken by means of basic laboratory equipment and reagents. The correlation between PHA content in wet cell samples and the spectra of the SB stained supernatant was determined by means of multivariate and linear regression analysis. The best calibration adjustment (R2 = 0.91, RSE: 1.56%), and the good PHA prediction obtained (RSE = 1.81%), shows that the proposed methodology constitutes a reasonably precise way for PHA content determination. Thus, this methodology could anticipate the probable results of the above mentioned direct PHA determination. Compared with the most used techniques described in the scientific literature, the combined implementation of these two methodologies seems to be one of the most economical and environmentally friendly, suitable for rapid monitoring of the intracellular PHA content. •Optimization process for Sudan black methodology for direct PHA quantification•Development of a methodology for the indirect determination of PHA content•Fast, simple, cheap and environmentally friendly methodologies that use basic equipment.•Combined methodologies can be implemented in parallel and at a very low cost.</description><identifier>ISSN: 0167-7012</identifier><identifier>EISSN: 1872-8359</identifier><identifier>DOI: 10.1016/j.mimet.2018.03.008</identifier><identifier>PMID: 29580981</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Azo Compounds - metabolism ; Bacillus megaterium - chemistry ; Chemometric ; Extractable poly(hydroxyalkanoate)s (PHAs) ; Naphthalenes - metabolism ; Polyhydroxyalkanoates - analysis ; Spectrophotometric methodology ; Spectrophotometry - methods ; Staining and Labeling - methods ; Sudan black stain</subject><ispartof>Journal of microbiological methods, 2018-05, Vol.148, p.1-11</ispartof><rights>2018 Elsevier B.V.</rights><rights>Copyright © 2018 Elsevier B.V. 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In a previous work it was shown that the PHA could be directly quantified using the absorbance of SB fixed by PHA granules in wet cell samples. In the present paper, the optimum SB amount and the optimum conditions to be used for SB assays were determined following an experimental design by hybrid response surface methodology and desirability-function. In addition, a new methodology was developed in which it is shown that the amount of SB fixed by PHA granules can also be determined indirectly through the absorbance of the supernatant obtained from the stained cell samples. This alternative methodology allows a faster determination of the PHA content (involving 23 and 42 min for indirect and direct determinations, respectively), and can be undertaken by means of basic laboratory equipment and reagents. The correlation between PHA content in wet cell samples and the spectra of the SB stained supernatant was determined by means of multivariate and linear regression analysis. The best calibration adjustment (R2 = 0.91, RSE: 1.56%), and the good PHA prediction obtained (RSE = 1.81%), shows that the proposed methodology constitutes a reasonably precise way for PHA content determination. Thus, this methodology could anticipate the probable results of the above mentioned direct PHA determination. Compared with the most used techniques described in the scientific literature, the combined implementation of these two methodologies seems to be one of the most economical and environmentally friendly, suitable for rapid monitoring of the intracellular PHA content. •Optimization process for Sudan black methodology for direct PHA quantification•Development of a methodology for the indirect determination of PHA content•Fast, simple, cheap and environmentally friendly methodologies that use basic equipment.•Combined methodologies can be implemented in parallel and at a very low cost.</description><subject>Azo Compounds - metabolism</subject><subject>Bacillus megaterium - chemistry</subject><subject>Chemometric</subject><subject>Extractable poly(hydroxyalkanoate)s (PHAs)</subject><subject>Naphthalenes - metabolism</subject><subject>Polyhydroxyalkanoates - analysis</subject><subject>Spectrophotometric methodology</subject><subject>Spectrophotometry - methods</subject><subject>Staining and Labeling - methods</subject><subject>Sudan black stain</subject><issn>0167-7012</issn><issn>1872-8359</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEFP3DAUhK0KVLa0v6BS5SOXpM-xk7UPHBBqCxJSK9GeLcd-6XqbxIvtUHHgv9fLUo6cLI2-eeMZQj4yqBmw7vO2nvyEuW6AyRp4DSDfkBWT66aSvFVHZFWodbUG1pyQdyltAVjLhXxLThrVSlCSrcjj9bSL4R4d9XOOxuI4LqOJ9MfVBXWYMU5-NtmHOdG_Pm_oXNiRph3aHMNuE3IoX4je0rvFzNkP3j7RtKib4MIYfntMtDepJBT5dnFmpv1o7B_qHvA9OR7MmPDD83tKfn398vPyqrr5_u368uKmsqVIrjrWWeE6sAqkEEI1xgppLQjRKWjdIE3TD71b94gKuCkSdkypzinomYOWn5Kzw93S9W7BlPXk076rmTEsSZcJFQiueFNQfkBtDClFHPQu-snEB81A73fXW_20-94kNXBddi-uT88BSz-he_H8H7oA5wcAS817j1En63G26HwsW2oX_KsB_wCJPJgv</recordid><startdate>201805</startdate><enddate>201805</enddate><creator>Porras, Mauricio A.</creator><creator>Villar, Marcelo A.</creator><creator>Cubitto, María A.</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0002-6249</orcidid></search><sort><creationdate>201805</creationdate><title>Improved intracellular PHA determinations with novel spectrophotometric quantification methodologies based on Sudan black dye</title><author>Porras, Mauricio A. ; Villar, Marcelo A. ; Cubitto, María A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-616c4d60c90844492ac48cc0446905df8a2bfbd7bee903a05de61996d90b1d053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Azo Compounds - metabolism</topic><topic>Bacillus megaterium - chemistry</topic><topic>Chemometric</topic><topic>Extractable poly(hydroxyalkanoate)s (PHAs)</topic><topic>Naphthalenes - metabolism</topic><topic>Polyhydroxyalkanoates - analysis</topic><topic>Spectrophotometric methodology</topic><topic>Spectrophotometry - methods</topic><topic>Staining and Labeling - methods</topic><topic>Sudan black stain</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Porras, Mauricio A.</creatorcontrib><creatorcontrib>Villar, Marcelo A.</creatorcontrib><creatorcontrib>Cubitto, María A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of microbiological methods</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Porras, Mauricio A.</au><au>Villar, Marcelo A.</au><au>Cubitto, María A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Improved intracellular PHA determinations with novel spectrophotometric quantification methodologies based on Sudan black dye</atitle><jtitle>Journal of microbiological methods</jtitle><addtitle>J Microbiol Methods</addtitle><date>2018-05</date><risdate>2018</risdate><volume>148</volume><spage>1</spage><epage>11</epage><pages>1-11</pages><issn>0167-7012</issn><eissn>1872-8359</eissn><abstract>The presence of intracellular polyhydroxyalkanoates (PHAs) is usually studied using Sudan black dye solution (SB). 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subjects Azo Compounds - metabolism
Bacillus megaterium - chemistry
Chemometric
Extractable poly(hydroxyalkanoate)s (PHAs)
Naphthalenes - metabolism
Polyhydroxyalkanoates - analysis
Spectrophotometric methodology
Spectrophotometry - methods
Staining and Labeling - methods
Sudan black stain
title Improved intracellular PHA determinations with novel spectrophotometric quantification methodologies based on Sudan black dye
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