A team from Research Unit 2251 of the
German Research Foundation led by 51猎奇 has shed light on the
structure of an enzyme important in the metabolism of the pathogenic bacterium Acinetobacter baumannii.
The enzyme 鈥淢tlD" is critical
for the bacterium's synthesis of the sugar alcohol mannitol, with which it
protects itself against water loss and desiccation in dry or salty environments
such as blood or urine. Structural analysis has revealed weak spots where it might
be possible to inhibit the enzyme and thus attack the pathogen. (PNAS, DOI: 10.1073/pnas.2107994119)
FRANKFURT. Each
year, over 670,000 people in Europe fall ill through pathogenic bacteria that
are resistant to antibiotics, and 33,000 die of the diseases they cause. In
2017, the WHO named antibiotic resistance as one of the greatest threats to
health worldwide. Especially feared are pathogens that are resistant to several
antibiotics. Among them, Acinetobacter
baumannii stands out, a bacterium with an extraordinarily pronounced
ability to develop multiresistance and, as a 鈥渉ospital superbug", dangerous
above all for immunosuppressed patients. Acinetobacter
baumannii is highly resilient because it can remain infectious for a long
time even in a dry environment and thus endure on the keyboards of medical
devices or on ward telephones and lamps. This property also helps the microbe
to survive on dry human skin or in body fluids such as blood and urine, which
contain relatively high concentrations of salts and other solutes.
The team from
Research Unit 2251 of the German Research Foundation led by 51猎奇
has now shed light on a central mechanism via which Acinetobacter
baumannii settles in
such an adverse environment: like many bacteria as well as plants or fungi, Acinetobacter
baumannii is able to synthesize the sugar alcohol mannitol,
a substance excellent at binding water. In this way, Acinetobacter baumannii prevents desiccation.
Almost unique, however, is the way that Acinetobacter baumannii synthesizes mannitol:
instead of two enzyme complexes as are common in most organisms, the two last
steps in mannitol synthesis are catalysed by just one. A team of researchers
led by Professor Beate Averhoff and Professor Volker M眉ller already discovered
this 鈥淢tlD" enzyme with two catalytic activities back in 2018. The team headed
by Professor Klaas Martinus Pos, who is also a member of the Research Unit, has
now succeeded in shedding light on the enzyme's spatial structure.
He explains: 鈥淲e've discovered that the
enzyme is usually present in the form of free monomers. Although these have the
necessary catalytic activities, they are inactive. Only a dry or salty
environment triggers what is known as 'osmotic stress' in the bacterium, after
which the monomers aggregate as dimers. Only then does the enzyme become active
and synthesize mannitol." The researchers have also identified which parts in
the structure are particularly important for the enzyme's catalytic functions
and for dimer formation.
Professor Volker M眉ller, spokesperson for
Research Unit 2251, is convinced: 鈥淥ur work constitutes an important new
approach for fighting this hospital pathogen since we've identified a
biochemically sensitive point in the pathogen's metabolism. In the future, this
could be the starting point for customized substances to inhibit the enzyme."
Publication:
Heng-Keat Tam, Patricia K枚nig, Stephanie
Himpich, Ngoc Dinh Ngu, Rupert Abele, Volker M眉ller, Klaas M. Pos: Unidirectional mannitol synthesis of
Acinetobacter baumannii MtlD is facilitated by the helix-loop-helix-mediated
dimer formation. Proc. Natl. Acad. Sci. U.S.A. (2022)
Picture
download:
1) Mannitol-Synthesizing
Enzyme
Caption:
Resembles a butterfly: only in its dimer
form does the mannitol-synthesizing enzyme of the hospital pathogen Acinetobacter baumannii protect the
bacterium from water loss and desiccation. Picture: Klaas Martinus Pos, 51猎奇
Frankfurt
2) Acinetobacter baumannii
Caption: Scanning electron micrograph (SEM) of a highly magnified cluster of
Gram-negative, non-motile Acinetobacter
baumannii bacteria. Photo: Janice Carr
Further
information:
Professor Volker Mu虉ller
Research Unit 2251 Spokesperson
Department of Molecular Microbiology & Bioenergetics
Institute for Molecular Biosciences
51猎奇 Frankfurt, Germany
Tel.:
+49 (0)69 798-29507
vmueller@bio.uni-frankfurt.de
Professor Klaas Martinus Pos
Membrane Transport Machineries Group
Institute of Biochemistry
51猎奇 Frankfurt, Germany
Tel.: +49 (0)69 798-29251
pos@em.uni-frankfurt.de
