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1.
Article in English | MEDLINE | ID: mdl-23859722

ABSTRACT

Adulteration of fruit juices--by the addition of sugar or other less expensive fruit juices as well as preservatives, artificial sweeteners and colours--was tested for by using a developed screening method. The method employs hydrophilic interaction liquid chromatography-mass spectrometry (HILIC-MS) using electrospray ionisation in the negative mode and ultraviolet light detection. Different fruit juices can be differentiated by the content of marker compounds like sorbitol, certain phenolic molecules and their saccharide profile. This method was used to test 46 fruit juice samples from the retail market as well as 12 control samples. The study focused on the main types of fruit juices consumed on the South African market including apple, orange, grape and blends of these juices with other fruits like mango, pear and guava. Overall, the 46 samples tested mostly agreed with label claims. One grape juice sample was adulterated, probably with apple juice. Natamycin above the legal limits was found in two samples. In addition, two samples contained natamycin and one sample benzoate without it being indicated on the label. The method is well suited as a quick screening method for fruit juice adulteration and if used routinely would reduce fruit juice adulteration without the cost of the current array of tests needed for authenticity testing.


Subject(s)
Beverages/analysis , Food Contamination/prevention & control , Food Inspection/methods , Fruit/chemistry , High-Throughput Screening Assays , Automation, Laboratory , Calibration , Chromatography, High Pressure Liquid , Food Additives/analysis , Food Contamination/legislation & jurisprudence , Food Labeling , Fungicides, Industrial/adverse effects , Fungicides, Industrial/analysis , Guideline Adherence , Legislation, Food , Limit of Detection , Pesticide Residues/adverse effects , Pesticide Residues/analysis , Principal Component Analysis , Quality Control , South Africa , Spectrometry, Mass, Electrospray Ionization , Spectrophotometry, Ultraviolet
2.
Antimicrob Agents Chemother ; 57(7): 3202-7, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23629716

ABSTRACT

Ergothioneine (ERG) and mycothiol (MSH) are two low-molecular-weight thiols synthesized by mycobacteria. The role of MSH has been extensively investigated in mycobacteria; however, little is known about the role of ERG in mycobacterial physiology. In this study, quantification of ERG at various points in the growth cycle of Mycobacterium smegmatis revealed that a significant portion of ERG is found in the culture media, suggesting that it is actively secreted. A mutant of M. smegmatis lacking egtD (MSMEG_6247) was unable to synthesize ERG, confirming its role in ERG biosynthesis. Deletion of egtD from wild-type M. smegmatis and an MSH-deficient mutant did not affect their susceptibility to antibiotics tested in this study. The ERG- and MSH-deficient double mutant was significantly more sensitive to peroxide than either of the single mutants lacking either ERG or MSH, suggesting that both thiols play a role in protecting M. smegmatis against oxidative stress and that ERG is able to partly compensate for the loss of MSH.


Subject(s)
Antioxidants/metabolism , Drug Resistance, Bacterial/genetics , Ergothioneine/metabolism , Mycobacterium smegmatis/metabolism , Bacterial Proteins/metabolism , Culture Media , Cysteine/metabolism , Ergothioneine/genetics , Glycopeptides/metabolism , Inositol/metabolism , Microbial Sensitivity Tests , Mutation , Mycobacterium smegmatis/drug effects , Mycobacterium smegmatis/genetics , Oxidative Stress
3.
Biotechnol J ; 3(11): 1424-8, 2008 Nov.
Article in English | MEDLINE | ID: mdl-19016512

ABSTRACT

A wide range of plant RNA extraction methods are available; however, many of these are limited in their application for a diverse range of plant species. With special emphasis on robustness and versatility, we have improved the cetyltrimethylammonium bromide (CTAB) method and isolated high-quality RNA from 16 different plant species. The major modifications made to the protocol described here were a reduction of sample treatment steps and an increase in beta-mercaptoethanol concentration (to 3%) resulting in a robust, rapid and reproducible plant RNA extraction protocol that can be used for a broad range of plant species and tissue types.


Subject(s)
Analytic Sample Preparation Methods/methods , Cetrimonium Compounds , Plant Leaves/chemistry , RNA, Plant/isolation & purification , Cetrimonium , Mercaptoethanol , Reverse Transcriptase Polymerase Chain Reaction/methods
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