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![Page 1: Siderophores and Metallophoresinoue/assets/img/archive-pdf/190105_LS.pdfJan. 5, 2019 | Literature Seminar The structure of the CntA-staphylopine-Co(II) complex (PDB ID: 5YHE):](https://reader034.vdocuments.us/reader034/viewer/2022042103/5e801b4e9f18f4466309742e/html5/thumbnails/1.jpg)
Jan. 5, 2019 | Literature Seminar
The structure of the CntA-staphylopine-Co(II) complex (PDB ID: 5YHE):Song, L.; Zhang, Y.; Chen, W.; Gu, T.; Zhang, S.-Y.; Ji, Q. Proc. Natl. Acad. Sci. USA 2018, 115, 3942.
Hiroaki Itoh
Siderophores and Metallophores
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Transition Metal Ions for Organisms
1) Waldron, K. J.; Rutherford, J. C.; Ford, D.; Robinson, N. J. Nature 2009, 460, 823. 2) Raymond, K. N.; Dertz, E.
A.; Kim, S. S. Proc. Natl. Acad. Sci. 2003, 100, 3584. 3) Yang, N.; Zhang, H.; Wang, M.; Hao, Q.; Sun, H. Sci.
Rep. 2012, 2, 999.
All organisms must acquire transition metals
(More than 30% of all proteins contain a transition metal cofactor)1)
e.g. iron
utilized as a cofactor of
hemeproteins (heme): hemoglobin,
cytochrome C
Fe(III) as free aqueous ion at pH 7.4:
10-18 M
Fe(III) in human serum:
10-24 M by the effect of transferrin
(iron transport protein)2)
diferric human serum transferrin and metal binding sites (PDB ID 3QYT)3)
Mechanisms for transition metal acquisition are required for each cell and the whole organisms
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Siderophores
Fe(III) in human serum: 10-24 M by the effect of
transferrin (iron transport protein)1)
transferrin
bacteria
host cell
siderophore
FeIII
Fe
Fe
FeFeIII
FeFeIII
uptake
endocytosis
stage 1
stage 2
1) Raymond, K. N.; Dertz, E. A.; Kim, S. S. Proc. Natl. Acad. Sci. 2003, 100, 3584.
Bacteria produce siderophores for uptake of iron
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Classification of Siderophores by Structures
enterobactin
(P. aeruginosa, E. coli, K. pneumoniae)
aerobactin
(K. pneumoniae, E. coli)
catecholate
hybrid (hydroxamate and carboxylate)
carboxylate
hybrid (phenolate and thiazoline)
yersiniabactin (K. pneumoniae)
staphyloferrin A
(S. aureus)
desferrioxamine B (Streptomyces sp.)
hydroxamate
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Biological Function of Siderophores
enterobactin:
produced by many Gram-negative bacteria
(Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumoniae,
Salmonella enterica etc.)
biosynthesis, transport, and process of enterobactin:1,2)
24 kb gene cluster
outer
membrane
inner
membrane
periplasm
EntS
FeIII
FepA
Fep
D
Fe
pG
(TolC-dependent) ?
Fes
FepC
FeIII
release of Fe(III)
1) Fischbach, M. A.; Lin, H.; Liu, D. R.; Walsh, C. T. Nat. Chem. Biol. 2006, 2, 132.
2) Lin, H.; Fischbach, M. A.; Liu, D. R.; Walsh, C. T. J. Am. Chem. Soc. 2005, 127, 11075.
EntB, EntE, EntF
ATP
ADP + Pi
cytoplasm
Fe:Fe FeFeIII
FeFeIIIFe
Fe FeFeIII
3× 3×3×
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Enterobactin is not Optimal Compounds in Hosts
1) Luo, M.; Lin, H.; Fischbach, M. A.; Liu, D. R.; Walsh, C. T.; Groves, J. T. ACS Chem. Biol. 2006, 1, 29.
2) Konopka, K.; Neilands, J. B. Biochemistry 1984, 23, 2122.
serum albumin
lipid bilayer
enterobactin: hydrophobic molecule
binding2)
partitioning1)
Enterobactins are captured by lipid bilayer and serum albumins in hosts
due to hydrophobic catechol moieties
iron acquisition rate constant (mM-1s-1) 0.041
membrane partitioning coefficient 15000
relative iron acquisition rate with 10 mM lipida 0.27
1)
aThe iron acquisition rate in the absence of lipid (SUVs
consisting of DMPC) are defined as 1.
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Host Defense System by Iron-binding Proteins
lactoferrin (PDB ID 1B0L)2)
neutrophil gelatinase-associated lipocalin
(NGAL)-Fe(III)-enterobactin complex1)
Sequestration of Fe(III)
1) Goetz, D. H.; Holmes, M. A.; Borregaard, N.; Bluhm, M. E.; Raymond, K. N.; Strong, R. K. Mol. Cell 2002, 10,
1033. 2) Sun, X. L.; Baker, H. M.; Shewry, S. C.; Jameson, G. B.; Baker, E. N. Acta Crystallogr. D Biol. Crystallogr.
1999, 55, 403.
Sequestration of Fe(III)-enterobactin complex
electrostatic potential (blue, positive; red, negative)
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Production of “Stealth” Siderophores
“stealth”
siderophores
lactoferrin
/transferrin
1) Wilson, B. R.; Bogdan, A. R.; Miyazawa, M.; Hashimoto, K.; Tsuji, Y. Trends Mol. Med. 2016, 22, 1077.
NGAL
bacteria
host cell
enterobactin
FeIII
Fe
Fe
FeFeIII
FeFeFeIII
FeIII
uptake
FeFeIII
uptake
endocytosis
endocytosisFe
FeFeFeIII
stage 1
stage 2
stage 3
stage 4
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Enzymatic Modification of Enterobactin
1) Bister, B.; Bischoff, D.; Nicholson, G. J.; Valdebenito, M.; Schneider, K.; Winkelmann, G.; Süssmuth, R. D.
BioMetals 2004, 17, 471.
enterobactin
(binder of NGAL)
salmochelin S4
(no binding to NGAL)
IroB1)
C-glycosylation
Fe
Fe
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Iron Uptake by Salmochelins
enterobactin
IroC
IroN?
IroD
release of Fe(III)salmochelin S4
1) Luo, M.; Lin, H.; Fischbach, M. A.; Liu, D. R.; Walsh, C. T.; Groves, J. T. ACS Chem. Biol. 2006, 1, 29.
2) Fischbach, M. A.; Lin, H.; Liu, D. R.; Walsh, C. T. Nat. Chem. Biol. 2006, 2, 132.
IroB
enterobactin salmochelin S4
iron acquisition rate constant (mM-1s-1) 0.041 0.045
membrane partitioning coefficient 15000 3100
relative iron acquisition rate with 10 mM lipida 0.27 0.64
aThe iron acquisition rate in the absence of lipid (SUVs consisting of DMPC) are
defined as 1.
Fe
outer
membrane
inner
membrane
periplasm
cytoplasm
Fe
Fe
Fe
FeIII
FeFeIII
FeFeIII
FeFeIII
?
FeIII + degradated
peptides
1)
2)
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Salmochelin is Essential for Virulence
1) Crouch, M.-L. V.; Castor, M.; Karlinsey, J. E.; Kalhorn, T.; Fang, F. C. Mol. Microbiol. 2008, 67, 971.
The biosynthesis and secretion of salmochelin S4 was found to play a role in the virulence1)
requirement for siderophore synthesis and secretion during systemic Salmonella
infection of mice
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Metallophores and Virulence
1) Remy, L.; Carrière, M.; Derré-Bobillot, A.; Martini, C.; Sanguinetti, M.; Borezée-Durant, E. Mol. Microbiol. 2013,
87, 730.
survival of mice infected with S. aureus bacterial counts within kidneys of mice
24 h after intravenous infection
square: wild type (RN6390), circles: cntABCDF mutant
A carrier of these heavy metals had been unknown
A nickel/cobalt uptake system (CntA, CntB, CntC, CntD, and CntF) in S. aureus
was found to play a role in the virulence in animal models of infection1)
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Nicotianamine-Like Molecule in Bacteria
1) Ghssein, G.; Brutesco, C.; Ouerdane, L.; Fojcik, C.; Izaute, A.; Wang, S.; Hajjar, C.; Lobinski, R.; Lemaire, D.;
Richaud, P.; Voulhoux, R.; Espaillat, A.; Cava, F.; Pignol, D.; Borezée-Durant, E.; Arnoux, P. Science 2016, 352,
1105.
nicotianamine: a metal chelator (copper, nickel, zinc, and iron) found in plants
biosynthesized by nicotianamine synthase
nicotianamine
A gene cording for nicotianamine synthase-like
enzyme was found in bacterial genome, including
that of S. aureus1)
ABC transporter: ATP-binding cassette transporters, MFS: major facilitator superfamily
1. cloning, expression and purification
of CntA from E. coli
2. incubation in supernatant of
S. aureus cntA mutant with Ni(II)
3. repurification of CntA
4. buffer exchange and MS analysis
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Discovery of Staphylopine
1) Ghssein, G.; Brutesco, C.; Ouerdane, L.; Fojcik, C.; Izaute, A.; Wang, S.; Hajjar, C.; Lobinski, R.; Lemaire, D.;
Richaud, P.; Voulhoux, R.; Espaillat, A.; Cava, F.; Pignol, D.; Borezée-Durant, E.; Arnoux, P. Science 2016, 352,
1105.
HILIC/ICP-MS chromatograms
HILIC/ESI-MS chromatogram (extracted ion chromatograms)
staphylopine
C13H19N4O6
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Biosynthesis of Staphylopine
1) Ghssein, G.; Brutesco, C.; Ouerdane, L.; Fojcik, C.; Izaute, A.; Wang, S.; Hajjar, C.; Lobinski, R.; Lemaire, D.;
Richaud, P.; Voulhoux, R.; Espaillat, A.; Cava, F.; Pignol, D.; Borezée-Durant, E.; Arnoux, P. Science 2016, 352,
1105. 15
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1) Ghssein, G.; Brutesco, C.; Ouerdane, L.; Fojcik, C.; Izaute, A.; Wang, S.; Hajjar, C.; Lobinski, R.; Lemaire, D.;
Richaud, P.; Voulhoux, R.; Espaillat, A.; Cava, F.; Pignol, D.; Borezée-Durant, E.; Arnoux, P. Science 2016, 352,
1105.
CntK: Histidine-Specific Racemase
CntK was found to be histidine-specific racemase
Marfey’s analysis (derivatization with FDAA)
Aeris peptide column 3.6 mm
4.6 x 250 mm
triethylamine phosphate buffer
/acetnitrile
2 mL/min
L-His
D-His
D-His + CntK
L-His + CntK
L-Ala
L-Met
L-His
D-His
L-His
D-His
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1) Ghssein, G.; Brutesco, C.; Ouerdane, L.; Fojcik, C.; Izaute, A.; Wang, S.; Hajjar, C.; Lobinski, R.; Lemaire, D.;
Richaud, P.; Voulhoux, R.; Espaillat, A.; Cava, F.; Pignol, D.; Borezée-Durant, E.; Arnoux, P. Science 2016, 352,
1105.
Functions of CntL and CntM
The results were consistent with the above
biosynthesis.
TLC analysis of reaction products incubating 14C-labelled
SAM with purified enzymes (CntK, CntL, and CntM), D-or L-
histidine, pyruvate, and NADPH
staphylopine
xNA
staphylopine
xNA
Dc
ntL
wild
typ
e
cn
tKL
M
S. aureusE. coli
TLC analysis of reaction products E. coli
cell extracts separately expressing CntK,
CntL, and CntM with 14C-labelled SAM
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Metal Selectivity of Staphylopine
pKd values for staphylopine complexes estimated by metal competition assay
with nicotianamine by ESI-MS
pKd (-log10Kd) at pH 7
staphylopine nicotianamine
Cu(II) 19.0 18.6
Ni(II) 16.4 16.1
Co(II) 15.1 14.8
Zn(II) 15.0 14.7
Fe(II) 12.3 12.1
Mn(II) 9.1 8.8
staphylopine has the similar Kd and affinity order:
Cu2+ > Ni2+ > Co2+ > Zn2+ > Fe2+ > Mn2+
(Fe(III) has a weak affinity for staphylopine at neutral pH)
staphylopine: a broad-spectrum metallophore, which is similar to nicotianamine
1) Ghssein, G.; Brutesco, C.; Ouerdane, L.; Fojcik, C.; Izaute, A.; Wang, S.; Hajjar, C.; Lobinski, R.; Lemaire, D.;
Richaud, P.; Voulhoux, R.; Espaillat, A.; Cava, F.; Pignol, D.; Borezée-Durant, E.; Arnoux, P. Science 2016, 352,
1105. 2) For metal selectivity of a related molecule, aspergillomarasamine A, see: Zhang, J.; Wang, S.; Bai, Y.;
Guo, Q.; Zhou, J.; Lei, X. J. Org. Chem. 2017, 82, 13643. 18
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Cellular Uptake of Metals
Intracellular metal content of the S. aureus was
determined by ICP-MS
left: wild type
middle: cntL mutant
right : cntABCDF mutant
These strains were grown in chemically defined
medium (CDM)
**P <0.01, ***P < 0.001
• Both cntL and cntA-F mutants caused decrease of intracellular accumulation of copper, nickel,
and cobalt
• A cntABCDF gene is involved with cellular uptake of metal or metal-staphylopine complexes
1) Ghssein, G.; Brutesco, C.; Ouerdane, L.; Fojcik, C.; Izaute, A.; Wang, S.; Hajjar, C.; Lobinski, R.; Lemaire, D.;
Richaud, P.; Voulhoux, R.; Espaillat, A.; Cava, F.; Pignol, D.; Borezée-Durant, E.; Arnoux, P. Science 2016, 352,
1105. 19
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Transportation of Metal-Staphylopine Complexes
chemically defined medium (CDM) supplemented
or not with 2 mM cobalt (Co), 10 μM of
staphylopine (Sp), or both (Co+Sp).
1) Ghssein, G.; Brutesco, C.; Ouerdane, L.; Fojcik, C.; Izaute, A.; Wang, S.; Hajjar, C.; Lobinski, R.; Lemaire, D.;
Richaud, P.; Voulhoux, R.; Espaillat, A.; Cava, F.; Pignol, D.; Borezée-Durant, E.; Arnoux, P. Science 2016, 352,
1105.
The addition of staphylopine restored the toxicity
of cobalt in cntL mutant but not in cntABCDF
A gene cntABCDF is likely involved with a
transportation of metal-staphylopine complexes
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Intracellular and Extracellular Staphylopines
staphylopine level of the intracellular (left)
and supernatant (right) fractions of the wild
type, cntABCDF, cntL, and cntE mutant
strains
*P <0.05, **P < 0.01; ND: not detected
These results supported that the functions of cntABCDF and cntE are involved with the import of
staphylopine-metal complexes and the export of staphylopine, respectively
cn
tE
cn
tAB
CD
F
cn
tL
wild
typ
e
cn
tE
cn
tAB
CD
F
cn
tL
wild
typ
e
1) Ghssein, G.; Brutesco, C.; Ouerdane, L.; Fojcik, C.; Izaute, A.; Wang, S.; Hajjar, C.; Lobinski, R.; Lemaire, D.;
Richaud, P.; Voulhoux, R.; Espaillat, A.; Cava, F.; Pignol, D.; Borezée-Durant, E.; Arnoux, P. Science 2016, 352,
1105. 21
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Biosynthesis and Function of Staphylopine
Homologous biosynthetic genes are encoded by other microbial pathogens, including
Psudomonas aeruginosa and Yersinia pestis
1) Ghssein, G.; Brutesco, C.; Ouerdane, L.; Fojcik, C.; Izaute, A.; Wang, S.; Hajjar, C.; Lobinski, R.; Lemaire, D.;
Richaud, P.; Voulhoux, R.; Espaillat, A.; Cava, F.; Pignol, D.; Borezée-Durant, E.; Arnoux, P. Science 2016, 352,
1105.
Further study on metallophores would reveal the influence of them in bacterial pathogenicity
22