Evidence map›Paper›PMID 26215140›Full record

ArticleMicrobial cell factories2015

Functionalized PHB granules provide the basis for the efficient side-chain cleavage of cholesterol and analogs in recombinant Bacillus megaterium.

Adrian Gerber, Michael Kleser, Rebekka Biedendieck, Rita Bernhardt, Frank Hannemann

Open access · goldAbstract read
In one paragraph

Article in Microbial cell factories, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.1field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Cytochrome P450The Journal of biological chemistry · 2025
    Article
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  8. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Adrian GerberCentre for Human and Molecular Biology, Institute of Biochemistry, Saarland University, 66123, Saarbrücken, Germany. a.gerber@mx.uni-saarland.de.
Michael KleserCentre for Human and Molecular Biology, Institute of Biochemistry, Saarland University, 66123, Saarbrücken, Germany. mic.kl@web.de.
Rebekka BiedendieckInstitute of Microbiology, Technische Universität Braunschweig, 38106, Braunschweig, Germany. r.biedendieck@tu-bs.de.
Rita BernhardtCentre for Human and Molecular Biology, Institute of Biochemistry, Saarland University, 66123, Saarbrücken, Germany. ritabern@mx.uni-saarland.de.
Frank HannemannCentre for Human and Molecular Biology, Institute of Biochemistry, Saarland University, 66123, Saarbrücken, Germany. f.hannemann@mx.uni-saarland.de.
Saarland University · DETechnische Universität Braunschweig · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCholesterol, the precursor of all steroid hormones, is the most abundant steroid in vertebrates and exhibits highly hydrophobic properties, rendering it a difficult substrate for aqueous microbial biotransformations. In the present study, we developed a Bacillus megaterium based whole-cell system that allows the side-chain cleavage of this sterol and investigated the underlying physiological basis of the biocatalysis.

resultsCYP11A1, the side-chain cleaving cytochrome P450, was recombinantly expressed in the Gram-positive soil bacterium B. megaterium combined with the required electron transfer proteins. By applying a mixture of 2-hydroxypropyl-β-cyclodextrin and Quillaja saponin as solubilizing agents, the zoosterols cholesterol and 7-dehydrocholesterol, as well as the phytosterol β-sitosterol could be efficiently converted to pregnenolone or 7-dehydropregnenolone. Fluorescence-microscopic analysis revealed that cholesterol accumulates in the carbon and energy storage-serving poly(3-hydroxybutyrate) (PHB) bodies and that the membrane proteins CYP11A1 and its redox partner adrenodoxin reductase (AdR) are likewise localized to their surrounding phospholipid/protein monolayer. The capacity to store cholesterol was absent in a mutant strain devoid of the PHB-producing polymerase subunit PhaC, resulting in a drastically decreased cholesterol conversion rate, while no effect on the expression of the recombinant proteins could be observed.

conclusionWe established a whole-cell system based on B. megaterium, which enables the conversion of the steroid hormone precursor cholesterol to pregnenolone in substantial quantities. We demonstrate that the microorganism's PHB granules, aggregates of bioplastic coated with a protein/phospholipid monolayer, are crucial for the high conversion rate by serving as substrate storage. This microbial system opens the way for an industrial conversion of the abundantly available cholesterol to any type of steroid hormones, which represent one of the biggest groups of drugs for the treatment of a wide variety of diseases.

Indexed as

2-Hydroxypropyl-beta-cyclodextrinBacillus megateriumbeta-CyclodextrinsBiocatalysisBiotransformationCholesterolCholesterol Side-Chain Cleavage EnzymeHydroxybutyratesPolyestersPolyhydroxybutyratesPregnenoloneProhibitinsQuillaja SaponinsRecombinant Proteins2-Hydroxypropyl-beta-cyclodextrinbeta-CyclodextrinsCholesterolCholesterol Side-Chain Cleavage EnzymeHydroxybutyratesPHB protein, humanpoly-beta-hydroxybutyratePolyestersPolyhydroxybutyratesPregnenoloneProhibitinsQuillaja SaponinsRecombinant Proteins

Identifiers

PMID26215140
PMCPMC4517628
OpenAlexW1858927617

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.