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Microbial Steroids

Overview of attention for book
Cover of 'Microbial Steroids'

Table of Contents

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    Book Overview
  2. Altmetric Badge
    Chapter 1 Steroid Bioconversions
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    Chapter 2 Chemical Pathways of Corticosteroids, Industrial Synthesis from Sapogenins
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    Chapter 3 Genome Sequencing of Steroid-Producing Bacteria with Illumina Technology
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    Chapter 4 Genome Sequencing of Steroid Producing Bacteria Using Ion Torrent Technology and a Reference Genome
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    Chapter 5 RNA-Seq-Based Comparative Transcriptomics: RNA Preparation and Bioinformatics
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    Chapter 6 Intra- and Extra-cellular Proteome Analyses of Steroid-Producer Mycobacteria
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    Chapter 7 Genetic Techniques for Manipulation of the Phytosterol Biotransformation Strain Mycobacterium neoaurum NRRL B-3805
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    Chapter 8 Identification and Characterization of the Genes and Enzymes Belonging to the Bile Acid Catabolic Pathway in Pseudomonas
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    Chapter 9 Selection of Biodegrading Phytosterol Strains
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    Chapter 10 Stigmasterol Removal by an Aerobic Treatment System
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    Chapter 11 Production and Biotransformation of Phytosterol Microdispersions to Produce 4-Androstene-3,17-Dione
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    Chapter 12 β-Sitosterol Bioconversion to Androstenedione in Microtiter Plates
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    Chapter 13 Bioconversion of Phytosterols into Androstenedione by Mycobacterium
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    Chapter 14 Scale-Up of Phytosterols Bioconversion into Androstenedione
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    Chapter 15 Bioconversion of Phytosterols into Androstadienedione by Mycobacterium smegmatis CECT 8331
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    Chapter 16 Process for Biotransformation of Androsta-4-ene-3, 17-Dione (4-AD) to Androsta-1,4-Diene-3,17-Dione (ADD)
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    Chapter 17 Laboratory-Scale Hydroxylation of Steroids by P450BM3 Variants
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    Chapter 18 Obtaining of 11α-Hydroxyandrost-4-ene-3,17-dione from Natural Sterols
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    Chapter 19 Steroid 11-Alpha-Hydroxylation by the Fungi Aspergillus nidulans and Aspergillus ochraceus
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    Chapter 20 Biotransformation of DHEA into 7α,15α-diOH-DHEA
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    Chapter 21 Stabilization of Enzymes by Using Thermophiles
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    Chapter 22 Biocatalysis of Steroids with Mycobacterium sp. in Aqueous and Organic Media
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    Chapter 23 Downstream Process Synthesis for Microbial Steroids
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    Chapter 24 Analysis of Intermediates of Steroid Transformations in Resting Cells by Thin-Layer Chromatography (TLC)
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    Chapter 25 A Ligand-Binding Assay to Measure the Affinity and Specificity of Sterol-Binding Proteins In Vitro
Attention for Chapter 13: Bioconversion of Phytosterols into Androstenedione by Mycobacterium
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Chapter title
Bioconversion of Phytosterols into Androstenedione by Mycobacterium
Chapter number 13
Book title
Methods in Molecular Biology
Published in
Methods in molecular biology, July 2017
DOI 10.1007/978-1-4939-7183-1_13
Pubmed ID
Book ISBNs
978-1-4939-7182-4, 978-1-4939-7183-1
Authors

Josefsen, Kjell D., Nordborg, Anna, Sletta, Håvard, Kjell D. Josefsen, Anna Nordborg, Håvard Sletta

Abstract

The chapter describes the bioconversion of phytosterols to androstenedione (AD) with Mycobacterium spp. in shake flasks and fermenters, as well as LC-MS based methods for analysis of phytosterols and steroid products.Phytosterols are derived as a by-product of vegetable oil refining and of manufacture of wood pulp. Phytosterols contain the same four-ring nucleus as steroids, and may be converted to high-value steroids by removing the side chain at C17 and minor changes at other sites in the ring structure.Many bacteria, including Mycobacterium spp., are able to degrade phytosterols. Mutants of Mycobacterium spp. unable of ring cleavage can, when growing on phytosterols, accumulate the steroid intermediates androstenedione (AD) and/or androstadienedione (ADD).The practical challenge with microbial conversion of phytosterols to steroids is that both the substrate and the product are virtually insoluble in water. In addition, some steroids, notably ADD, may be toxic to cells.Two main strategies have been employed to overcome this challenge: the use of two-phase systems, and the addition of chemically modified cyclodextrins. The latter method is used here.Defined cultivation and bioconversion media for both shake flask and fermenter are given, as well as suggestions to minimize the practical problems caused by the water-insoluble phytosterol. Sampling, sample extraction, and quantification of substrates and products using LC-MS analysis are described.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 18 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 18 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 5 28%
Researcher 4 22%
Professor > Associate Professor 2 11%
Student > Master 1 6%
Student > Doctoral Student 1 6%
Other 2 11%
Unknown 3 17%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 6 33%
Chemistry 2 11%
Agricultural and Biological Sciences 2 11%
Chemical Engineering 1 6%
Environmental Science 1 6%
Other 2 11%
Unknown 4 22%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 16 July 2017.
All research outputs
#20,434,884
of 22,988,380 outputs
Outputs from Methods in molecular biology
#9,931
of 13,150 outputs
Outputs of similar age
#272,116
of 312,216 outputs
Outputs of similar age from Methods in molecular biology
#212
of 274 outputs
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So far Altmetric has tracked 13,150 research outputs from this source. They receive a mean Attention Score of 3.4. This one is in the 1st percentile – i.e., 1% of its peers scored the same or lower than it.
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We're also able to compare this research output to 274 others from the same source and published within six weeks on either side of this one. This one is in the 1st percentile – i.e., 1% of its contemporaries scored the same or lower than it.