In:
eLife, eLife Sciences Publications, Ltd, Vol. 8 ( 2019-01-14)
Abstract:
Gram-negative bacteria are a large group of single-celled organisms that share a typical external envelope. This casing is formed of an inner and an outer membrane, which have different structures and properties. The outer membrane lets nutrients penetrate inside the cell, but blocks out other compounds, such as antibiotics. It is made of a complex assembly of molecules, including glycerolphospholipids (GPL) that are produced inside the cells. Very little is known about how this external shield is created and maintained. For example, it was still unclear how GPLs were exported through the inner membrane to the outer one. To investigate these questions, Kamischke et al. exposed a species of Gram-negative bacteria to a molecule that is normally blocked by the outer membrane. If the outer membrane is not working properly, the compound can cross it and the cell turns blue. Kamischke et al. then introduced genetic changes at random locations in the genomes of the bacteria. If colonies became blue, this meant that the mutations had happened in a gene essential for the outer membrane. Sequencing these blue bacteria revealed 58 genes involved in keeping the outer membrane working properly. Amongst them, four genes coded for a transport machine, the Mla system, which allowed GPLs to cross the inner membrane and reach the outer membrane. The experiments also showed that a working Mla system was required for bacteria to survive antibiotics. Certain dangerous Gram-negative bacteria are now resistant to many drugs, having evolved unique envelopes that keep antibiotics at bay. By learning more about the outer membrane, we may be able to create new treatments to bypass or to disable this shield, for example by targeting the Mla system.
Type of Medium:
Online Resource
ISSN:
2050-084X
DOI:
10.7554/eLife.40171.001
DOI:
10.7554/eLife.40171.002
DOI:
10.7554/eLife.40171.003
DOI:
10.7554/eLife.40171.004
DOI:
10.7554/eLife.40171.005
DOI:
10.7554/eLife.40171.006
DOI:
10.7554/eLife.40171.007
DOI:
10.7554/eLife.40171.008
DOI:
10.7554/eLife.40171.009
DOI:
10.7554/eLife.40171.010
DOI:
10.7554/eLife.40171.011
DOI:
10.7554/eLife.40171.012
DOI:
10.7554/eLife.40171.013
DOI:
10.7554/eLife.40171.014
DOI:
10.7554/eLife.40171.015
DOI:
10.7554/eLife.40171.016
DOI:
10.7554/eLife.40171.017
DOI:
10.7554/eLife.40171.018
DOI:
10.7554/eLife.40171.019
DOI:
10.7554/eLife.40171.020
DOI:
10.7554/eLife.40171.021
DOI:
10.7554/eLife.40171.022
DOI:
10.7554/eLife.40171.023
DOI:
10.7554/eLife.40171.029
DOI:
10.7554/eLife.40171.030
Language:
English
Publisher:
eLife Sciences Publications, Ltd
Publication Date:
2019
detail.hit.zdb_id:
2687154-3
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