Literature DB >> 6714026

Use of flow cytometry in industrial microbiology for strain improvement programs.

J W Betz, W Aretz, W Härtel.   

Abstract

A flow cytometry (FCM) system was chosen to analyze and sort microbiological samples, e.g., bacteria, bacterial spores, yeasts, and fungal spores, without major changes in the commercially available state. The system was further improved by addition of a stepping motor-driven scanning table that accepts standard petri dishes or microtiter plates. The electronics of the sorting system were changed to enable the sorter to deliver only one particle at a time, working in a "handshake" mode with the scanning table. Appropriate parameters, depending on the biological material and including all fluorescent stains that do not impair growth and productivity of cells were chosen to sort distinct bioparticles under aseptic conditions and to clone colonies or cultures out of them. A mutagenized sample of spores entering the germination cycle can be followed and thus provide a means to pick only viable growing cells despite the killing effect of the mutagen. One example of a typical strain improvement is illustrated. From a spore suspension of Rhizopus arrhizus, a subpopulation of morphologically different spores comprising about 5-10% of the whole population was cloned. From approximately 8,000 clones, 10 were isolated that produced approximately five- to six-fold the amount of fungal lipase activity, compared to the original strain or to reisolated clones from the mean population of clones.

Entities:  

Mesh:

Year:  1984        PMID: 6714026     DOI: 10.1002/cyto.990050208

Source DB:  PubMed          Journal:  Cytometry        ISSN: 0196-4763


  7 in total

Review 1.  Quantifying heterogeneity: flow cytometry of bacterial cultures.

Authors:  D B Kell; H M Ryder; A S Kaprelyants; H V Westerhoff
Journal:  Antonie Van Leeuwenhoek       Date:  1991 Oct-Nov       Impact factor: 2.271

Review 2.  Flow cytometry and cell sorting of heterogeneous microbial populations: the importance of single-cell analyses.

Authors:  H M Davey; D B Kell
Journal:  Microbiol Rev       Date:  1996-12

3.  Flow cytometric screening and isolation of Escherichia coli clones which express surface antigens of the oil-degrading microorganism Acinetobacter calcoaceticus RAG-1.

Authors:  W Minas; E Sahar; D Gutnick
Journal:  Arch Microbiol       Date:  1988       Impact factor: 2.552

Review 4.  Applications of flow cytometry to clinical microbiology.

Authors:  A Alvarez-Barrientos; J Arroyo; R Cantón; C Nombela; M Sánchez-Pérez
Journal:  Clin Microbiol Rev       Date:  2000-04       Impact factor: 26.132

5.  Binge eating disorder.

Authors:  Katrin E Giel; Cynthia M Bulik; Fernando Fernandez-Aranda; Phillipa Hay; Anna Keski-Rahkonen; Kathrin Schag; Ulrike Schmidt; Stephan Zipfel
Journal:  Nat Rev Dis Primers       Date:  2022-03-17       Impact factor: 52.329

6.  Isolation of a gramicidin S hyperproducing strain of Bacillus brevis by use of a fluorescence activated cell sorting system.

Authors:  T Azuma; G I Harrison; A L Demain
Journal:  Appl Microbiol Biotechnol       Date:  1992-11       Impact factor: 4.813

7.  Sorting of Streptomyces cell pellets using a complex object parametric analyzer and sorter.

Authors:  Marloes L C Petrus; G Jerre van Veluw; Han A B Wösten; Dennis Claessen
Journal:  J Vis Exp       Date:  2014-02-13       Impact factor: 1.355

  7 in total

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