Patent Application
20190085338
A computer readable text file, entitled “SequenceListing.txt,” created on or about Jun. 13, 2018 with a file size of about 18 kb contains the sequence listing for this application and is hereby incorporated by reference in its entirety.
The present invention relates to bacteria engineered to synthesize compounds which increase their ability to resist as well as to take up cobalt and/or nickel from their environment. More specifically, the invention concerns magnetotactic bacteria modified to express metallophores and their use in bioremediation, biodetection, imaging, as well as the use of magnetosomes extracted from such bacteria in several indications including antitumor treatment and in a process of metal recovery.
Magnetotactic bacteria (or MTB) are a polyphyletic group of Gram-negative bacteria discovered by Richard P. Blakemore in 1975. They passively align and actively swim along the geomagnetic field and other magnetic fields. This unique feature is based on specific intracellular organelles, the magnetosomes, which, in most MTB, comprise nanometer-sized, membrane bound crystals of magnetic iron and are organized into chains via a dedicated cytoskeleton.
Because of the special properties of the magnetosomes, MTB are of great interest for paleomagnetism, environmental magnetism, biomarkers in rocks, magnetic materials and biomineralization in organisms; bacterial magnetite has been exploited for a variety of applications in modern biological and medical sciences.
MTB can be found in freshwater and salt water, and in oxygen rich as well as anoxic zones at depths ranging from the near-surface to 2000 meters beneath the surface. However, the majority of MTB discovered so far gather at the so-called oxic-anoxic transition zone. They can be spiral-shaped, rods and spheres.
The present invention concerns a genetically modified magnetotactic bacteria (MTB) expressing a cobalt and/or nickel-specific metallophore.
As used herein, a “cobalt and/or nickel-specific metallophore” is a compound able to form a complex with a cobalt or a nickel ion. Such metallophore may be able to bind cobalt or nickel, or both.
The inventors have previously identified two compounds able to chelate cobalt and nickel. These metallophores are synthesized by two bacteria: Staphylococcus aureus and Pseudomonas aeruginosa, and have been respectively named staphylopine and pseudopaline.
In one embodiment, the genetically modified MTB of the invention produces a molecule of formula (I):
Among the molecules of formula (I), two preferred molecules are staphylopine and pseudopaline. Thus, in a preferred embodiment, the invention concerns a genetically modified MTB expressing a metallophore which is staphylopine of formula (II):
In another preferred embodiment, the invention concerns a genetically modified MTB expressing a metallophore which is pseudopaline of formula (III):
The inventors have shown that bacteria able to produce a metallophore can be obtained by introducing the genes responsible for the biosynthesis of said metallophores into the bacteria. In particular, they demonstrated that:
Thus, in a particular embodiment, the invention concerns a genetically modified MTB expressing genes encoding the proteins of Staphylococcus aureus of SEQ ID NO: 1, SEQ ID NO: 2 and SEQ ID NO: 3 or variants thereof. Such a bacterium produces staphylopine. In another particular embodiment, the invention concerns a genetically modified MTB expressing genes coding the proteins of Pseudomonas aeruginosa of SEQ ID NO: 4 and SEQ ID NO: 5 or variants thereof. Such a bacterium produces pseudopaline.
The invention also concerns a genetically modified magnetotactic bacterium characterized in that it expresses a cobalt and/or nickel-specific metallophore, wherein the metallophore is chosen among staphylopine and pseudopaline, and (i) when the metallophore is staphylopine, said bacteria expresses the proteins of SEQ ID NO:1, SEQ ID NO:2 and SEQ ID NO:3 or variants thereof, and (ii) when the metallophore is pseudopaline, said bacteria expresses the proteins of SEQ ID NO: 4 and SEQ ID NO: 5 and variants thereof.
As used herein, the term “variant” corresponds to a sequence which differs by at least one amino acid from the sequence of reference, provided that the function of the protein is retained. An homologous sequence can, for example, be qualified of variant. Also modified or isoform sequences having retained at least one of the properties that make them biologically active are encompassed in the scope of this definition. Typically, a variant sequence presents at least 40%, 50%, 60%, 70%, 75%, 80%, 85%, 90%, 95%, 98% or 99% of identity with the protein of reference, as measured by BLAST method. In a preferred embodiment, a variant sequence presents at least 40% of identity with the sequence of reference. Further, for example, a protein having a sequence identical to SEQ ID NO: 1 and a tag at its N-terminal or C-terminal extremity is a variant of SEQ ID NO: 1, provided that it conserves its activity. For example, a variant of the protein of SEQ ID NO: 1, when co-expressed in a bacterium with the proteins of SEQ ID NOs: 2 and 3, enables the biosynthesis of staphylopine by said bacterium.
It has been previously shown that the two preferred metallophores of the invention, staphylopine and pseudopaline, are able to chelate both cobalt and nickel.
At relatively high concentration, cobalt and nickel are toxics to bacteria. The degree of toxicity is metal-dependent. For example, cobalt is more toxic than nickel.
The inventors of the present invention have demonstrated that expressing these metallophores in magnetotactic bacteria allows to increase their resistance to cobalt and to nickel.
MTB is a large group of bacteria wherein only a limited number have been isolated in pure cultures so far. Among them, Magnetospirillum gryphiswaldense MSR-1, Magnetospirillum magneticum AMB-1, Magnetospirillum magneticum MGT-1, Magnetovibrio MV-1, Magnetococcus sp. MC-1, Marine magnetic spirillum QH-2, Magnetospirillum sp. WM-1 and Magnetospirillum magnetotacticum MS-1 are all affiliated to the α-Proteobacteria; Desulfovibrio magneticus RS-1 is affiliated to the β-Proteobacteria. These and any other MTB can be used in the frame of the present invention.
According to a preferred embodiment, the genetically modified MTB used in this invention are Magnetospirillum gryphiswaldense MSR-1 or Magnetospirillum magneticum AMB-1.
In addition, genetically modified MTB expressing genes responsible for the biosynthesis of a cobalt and/or nickel-specific metallophore from other bacteria than Staphylococcus aureus and Pseudomonas aeruginosa, for example homologous genes from Serratia marcescens or Yesinia pestis, are also part of the invention.
The present invention also concerns MTB which have acquired new properties.
The inventors have demonstrated that genetically modified MTB able to synthesize staphylopine or pseudopaline present unexpected properties relating to their capacity to both resist to metal and accumulate metal.
In particular, a genetically modified MTB of the invention is more resistant to cobalt and/or nickel than the parent magnetotactic strain which does not express the metallophore.
This property is illustrated in the experimental part, especially on
A used herein, “a bacteria that is more resistant to metal than the parent strain” corresponds to a bacteria which is able to survive in a medium containing a concentration of metal lethal for the parent strain. Most of the time, this strain is able to grow better than the parent strain when placed in sublethal concentrations of such metal. Such a strain is also a strain which will survive longer than the parent strain in an environment containing metal.
Thus, in a particular embodiment, a genetically modified MTB of the invention which is more resistant to cobalt and or nickel than the parent magnetotactic strain can be a recombinant M. gryphiswaldense MSR-1 or M. magneticum AMB-1.
In another particular embodiment, a genetically modified MTB of the invention which is more resistant to cobalt and/or nickel than the parent magnetotactic strain synthesizes staphylopine or pseudopaline.
In a further embodiment, a genetically modified MTB of the invention which is more resistant to metal than the parent magnetotactic strain is indeed more resistant to cobalt.
In a further embodiment, a genetically modified MTB of the invention which is more resistant to metal than the parent magnetotactic strain is indeed more resistant to nickel.
In a further embodiment, a genetically modified MTB of the invention which is more resistant to metal than the parent magnetotactic strain is indeed more resistant to both cobalt and nickel.
In another aspect of the invention, a genetically modified MTB of the invention accumulates higher quantity of cobalt and/or nickel than the parent strain.
In a particular embodiment, a genetically modified MTB of the invention exhibit a cobalt or nickel accumulation capacity that is at least 20% superior to the cobalt accumulation capacity of the parent strain which does not produce the metallophore.
In a particular embodiment, a genetically modified MTB expresses pseudopaline and the cobalt accumulation is at least twice higher than the cobalt accumulation in the parent strain (
In another particular embodiment, a genetically modified MTB expresses staphylopine and the cobalt accumulation is at least three times higher than the cobalt accumulation in the parent strain.
The cobalt accumulation in these bacteria can even be more than three times higher than in parent strain (
In another embodiment, a genetically modified MTB expresses pseudopaline or staphylopine and the nickel accumulation is higher than the nickel accumulation in the parent strain (
This nickel accumulation is at least 30% higher than the nickel accumulation in the parent strain.
In another aspect of the invention, a genetically modified MTB of the invention accumulates cobalt and/or nickel in the magnetosomes.
In a particular embodiment, such bacteria contain at least 50 ng of cobalt per mg dry weight. In a preferred embodiment, such bacteria contain at least 75 ng of cobalt per mg dry weight, as illustrated in
In further embodiment, the invention concerns a recombinant MTB expressing a cobalt and/or nickel specific metallophore and a cobalt and/or nickel permease.
As used herein, a “cobalt and/or nickel permease” is a permease located at the cellular membrane which is specific for cobalt and nickel importation.
The inventors have demonstrated that a recombinant MTB expressing both a metallophore and a cobalt and/or nickel permease presents an improved resistance to metal and a higher accumulation capacity than the parent MTB strain and than the MTB expressing only a metallophore.
In a particular embodiment, the cobalt and/or nickel permease is encoded by the NxiA gene. In a particular embodiment, the NxiA gene is from Rhodopseudomonas palutris and corresponds to the sequence SEQ ID NO: 10.
The NxiA permease belongs to a gene family also retrieved in several bacterial strains as for example in H. pylori, N. aromaticivirans, R. rodochrous and R. pulustris . . . In R. palustris (CGA009 strain), this permease is identified in the public database Cyanobase (http://genome.microbedb.jp/CyanoBase) as “RPA0724 gene” and as corresponding to nxiA (in H. pylori), nixA (in S. aureus), HoxN (in R. rhodochrous) and NhIF (in R. Eutropha). All these genes code for cobalt and/or nickel permeases. The use of these permeases for the bioremediation is known from literature; they can be used in the frame of the invention.
According to the above-described features, a recombinant MTB of the invention thus corresponds a bacteria which expresses a metallophore or to a bacteria which expresses both a metallophore and a cobalt and/or nickel permease.
In another aspect, the invention also concerns magnetosomes extracted from the magnetotactic bacteria of the invention. These magnetosomes are made of a proteo-lipidic membrane surrounding a single crystal of magnetite. The biosynthesized magnetite is of higher purity than chemically synthesized ones and has also a narrow size range of 50-100 nm, which participates to its singular properties when compared to chemically synthesized magnetite.
Thus, in a particular embodiment, the invention concerns a nickel- or cobalt-doped magnetosome isolated from a genetically modified MTB of the invention, especially when isolated from bacteria having accumulated cobalt and/or nickel. Such doped-magnetosomes can thus be extracted from bacteria expressing a metallophore or from bacteria expressing both a metallophore and a cobalt and/or nickel permease.
As used herein, a “doped-magnetosome” according to this invention contains at least 20% more cobalt than a magnetosome from a MTB non-expressing a metallophore. In particular, the quantity of cobalt contained in a magnetosome can be measured by comparison to the quantity of iron; the quantity of iron being not modified by the expression of metallophore, it can be used as a reference to evaluate the accumulation of cobalt or nickel. Using this system, the inventors have shown that the MTB producing staphylopine and/or pseudopaline can accumulate in their magnetosomes a relative quantity of cobalt/iron around 1.3% whereas this ratio is of 1% in non-recombinant MTB (Table 4).
Thus, in one embodiment, the invention concerns a cobalt- and/or nickel-doped magnetosome. Such magnetosome can be defined as presenting a ratio cobalt/iron of at least 1.25.
Further, magnetosomes extracted from bacteria expressing both a metallophore and a cobalt and/or nickel permease contain a higher quantity of cobalt and/or nickel than those extracted from bacteria expressing only a metallophore. Such magnetossome may contain at least 25%, and preferably 30%, preferably 40%, and even more preferably 50% more cobalt than a magnetosome from a parent MTB. Further, they present a ratio cobalt/iron of at least 1.5, more preferably of at least 2.
Another aspect of the invention concerns the use of cobalt- and/or nickel-doped magnetosome isolated from a MTB of the invention in antitumor treatment.
Indeed, bacterial magnetosomes can efficiently be used to generate heat in a solution when exposed to an alternative magnetic field. For anti-tumoral application, magnetosomes can be used as such or encapsulated within a vesicule and possibly targeted by any appropriate means including for example antibody, aptamer, recombinant protein, synthetic molecule . . .
The antitumor treatment can be administered directly to the patient for in vivo treatment. The heat treatment is generated by applying a magnetic field which provokes the production of heat by magnetosomes. The frequency of such magnetic field should lie between about 50 kHz and 1000 kHz, preferably between about 100 kHz and 500 kHz, more preferably between about 100 hKz and 200 kHz. The strength of the magnetic field is comprised between about 0.1 mT and 200mT, preferably between 1 mT and 100 mT, more preferably between about 10 mT and 60 mT.
A person skilled in the art would know how to determine the appropriate characteristic of the magnetic field in order to obtain an efficient heat but without toxic side-effects. The thermotherapy can be optimized by adjusting the different parameters including the amount of magnetosomes administered to the patient, the characteristics of the magnetic field, the duration of the application of the magnetic field and the protocol of the treatment regarding the number of repetitions of the treatment (i.e., one application or repeated ones).
This invention also concerns the use of nickel- or cobalt-doped magnetosome isolated from MTB of the invention, in imaging.
An example of imaging application is now described. The membrane surface of the magnetosomes allows the attachment of specific bacteriophages expressing targeting molecules such as antibodies. In addition, it is possible to rely on the magnetic properties conferred by the magnetism to control the bacteria's moving by applying an alternative magnetic field. Thus, one can surround a defined area using the MTB. If a bacteriophage-magnetosome complex meets a cell or molecule of interest, the magnetosome will stick on it through the bacteriophage. Then, the cell or molecule of interest can be detected by using magnetics crystals as contrast agent. Examples of other applications of MTB in imaging are the direct use of their magnetosomes as a contrast agent. Indeed magnetosomes are ultrasensitive magnetic resonance imaging (MRI) T2-contrast agents.
In a further aspect, the invention concerns the use of a bacterium according to the invention in bioremediation of cobalt and/or nickel.
For almost a century, intense human activities such as mining, chemical industries and intensive agriculture led to high accumulation of toxic metals in the environment. These toxic metals are difficult to remove from the environment, since they cannot be easily degraded and are ultimately indestructible. In this context, the inventors of the present application have proposed an efficient bioremediation process. For example, MTB engineered to produce pseudopaline or staphylopine could be grown in liquid media containing nickel and cobalt at subtoxic levels. Because these bacteria accumulate more metal, they can be used to extract these metals from the liquid solution. Furthermore, in another aspect, the present invention concerns a process of recovery of cobalt and/or nickel contained in the MTB.
The aim of this process is to provide a system which allows an easy recovery of metal present in a liquid medium using a magnet. With this aim, the inventors proposed to use MTB expressing a metallophore to recover metal for the environment.
In a preferred embodiment, the metallophore is staphylopine or pseudopaline and the metal trapped in the magnetosome is cobalt and/or nickel.
In a particular embodiment, a process of recovery of cobalt and/or nickel of the invention comprises the following steps: (i) contacting bacteria according to the invention with a medium containing cobalt and/or nickel, and (ii) after an incubation period, creating a magnetic field to recover bacteria containing cobalt and/or nickel.
The process of recovery of cobalt and/or nickel of the invention can be applied to any liquid medium containing such a metal. In a preferred embodiment, this medium containing cobalt and/or nickel from which this metal is recovered is a medium to be depolluted.
The incubation period can be between 3 hours (accumulation was demonstrated at this short period of time) to 120 Hours (cells begin to suffer and die after this period). A preferred incubation duration can be at least between 24 h and 90 h, for example of 48 h, 60 h or 72 h. A preferred incubation duration is 72 Hours.
The medium to be depolluted can be any liquid medium containing cobalt and/or nickel such as cooling water or radioactive waste from nuclear plants (mainly cobalt) or contaminated sludges from battery factories (mainly nickel).
Another aspect of the invention concerns the use of a recombinant MTB according to the invention as a biodetector for cobalt and/or nickel traces.
Indeed, a bacteria expressing a metallophore has the ability to take up cobalt and/or nickel from the environment and to concentrate it intracellularly. The presence of cobalt and/or nickel can then be detecting for example by introducing a reporter gene placed under the control of a promoter sensitive to cobalt and/or nickel. Such promoter can be for example the promotor controlling the expression of the nikABCDE Ni-uptake operon, or the promotor controlling the rcnAB operon which encodes a Ni and Co efflux system (Cayron J. et al., Environ Sci Pollut Res Int. 2015). According to this embodiment, the recombinant MTB strain of the invention can be used to detect very low quantity of cobalt and/or nickel.
A recombinant strain expressing both a metallophore and a reporter construct comprising a promoter sensitive to cobalt and/or nickel, is also part of the invention.
The invention will now be described in further details using the following non-limiting examples.
a. Description of the Genes
Two genes from Pseudomonas aeruginosa (PA4836 and PA4835) are responsible for the pseudopaline biosynthesis. Three genes from Staphylococcus aureus (SAV2470, SAV2469 and SAV2468) are responsible for staphylopine biosynthesis. One of these genes encodes a histidine racemase (SAV2470), two others encode Nicotianamine-like synthases (PA4836 and SAV2469) and finally the two remaining enzymes (PA4835 and SAV2468) encode a member of the DUF2338 family experimentally identified as a N-(CA)amino acid dehydrogenases. These enzymes (and their corresponding genes) are the hallmark of a bacterial metallophore biosynthetic machinery. Hereafter, for clarity, the two genes from Pseudomonas aeruginosa are named « paND » (for P. aeruginosa Nas-like and DUF2338 coding genes) and the three genes from Staphylococcus aureus are named « saEND » (for S. aureus Epimerase, Nas-like and DUF2338 coding genes).
b. Description of Gene Constructs
Plasmids have been designed in the laboratory and ordered at Genecust ©. They contain the DNA sequence of the genes from S. aureus Mu50 and P. aeruginosa PA-01 integrated into the broad host plasmid pBBR1-MCS2. The genes have been inserted downstream two promoters: 1/the lac promoter for the expression of the genes in E. coli 2/the promoter mamGFDC of Magnetospirillum gryphyswaldense for the expression of the genes in magnetotactic bacteria. The constructs designed for expressing the genes in magnetotactic bacteria are reproduced in
Transfer of the genetic constructions as described in Example 1, in magnetotactic bacteria (M. gryphyswaldense MSR-1 and Magnetospirillum magneticum AMB-1) has been done by conjugation of the magnetotactic strain using a strain of E. coli previously transformed with the genes constructs and harboring the genes tra required for conjugation. Thus, the strain E. coli WM3064 was chosen for its ability to transfer pBBR1-MCS2 in a large variety of hosts (including magnetotactic bacteria) with a counter-selection in a medium devoid of diaminopimelate, the strain being auxotrophic toward this molecule.
Both 1 mL of overnight culture of magnetotactic bacteria and 200 μL of an overnight culture of E. coli strain WM3064 carrying the pBBR1-MCS2 constructs have been collected and resuspended in 30 μL of appropriate medium (see below) supplemented with diaminopimelate (0.3 mM). The 30 μL of mixed bacteria have been disposed on an agar plate of appropriate medium supplemented with 0.3 mM diaminopimelate, and left at 30° C. for 24 H. The cells have then been collected and plated on solid medium with antibiotic and without diamniopimelate, thus ensuring the selection of magnetotactic bacteria carrying the pBBR1-MCS2 construct, and eliminating the E. coli strain. Magnetotactic strains have then been selected and screened for the plasmid presence and the integrity of the construction by simple PCR amplification of the paND fragment.
Primers used to amplify the paND sequence are the following:
M. gryphyswaldense MSR-1 and M. magneticum AMB-1 have been cultivated respectively in MSR-1 lactate medium pH 7 and MagMin 1.5 medium pH 6.9. MSR-1 lactate: (HEPES 10 mM, Na-lactate 0.15%, Soja-Peptone 0.3% Yeast extract 0.01%, NaNO3 4 mM, KH2PO4 0.7 mM, MgSO4 0.6 mM, Fe-citrate 50 μM, and 0.1% Trace Element Solution : H3Bo3 162 μM, Na2MoO4 74 μM, ZnSO4 250 μM, CuCl2 6 μM, NiCl2 50 μM, CoCl2 400 μM, MnCl2 250 μM, Na2EDTA 7 mM).MagMin 1.5: (KH2PO4 5 mM, NaNO3 1.5 mM, Na Acetate 850 μM, Ascorbic acid 0.2 mM, Tarataric acid 2.5 mM, Succinic acid 3.1 mM, Na thiosulfate 0.2 mM, 0.5% Modified Mineral Wolf Elixir:Nitrilotriacetic acid (NTA) 7.8 mM, MgSO412.2 mM, MnSO4 2.9 mM, NaCI 17 mM, FeSO4 360 μM, CoCl2 420 μM, CaCl2 680 μM, ZnSO4 348 μM, CuSO4 100 μM, AIK(SO4)2 21 μM, H3BO3 162 μM, Na2MoO4 1.65 mM, NiCl241 μM).
All strains have been cultivated under microaerophilic conditions (O2=2%) at 30° C. with the appropriate antibiotic.
25 mL of medium supplemented with different metals have been inoculated at a final OD600nm=0.1 for M. gryphiswaldense MSR-1 and OD600nm=0.03 for M. magneticum AMB-1 with an overnight preculture. Growth was then followed by measurement of optical density at 600 nm.
As shown in
From
In the case of resistance toward nickel, strain MSR-1 show a better growth when producing pseudopaline than when producing staphylopine.
Both strains, in the presence of cobalt or nickel, present better growth than the control strain.
The magnetotactic strains expressing the genes coding for the biosynthesis of pseudopaline and staphylopine resist to higher concentration of nickel and cobalt.
Magnetotactic strains have been cultivated in the appropriate medium (at least 200 mL) in the presence of cobalt (100 μM CoCl2) or nickel (500 μM NiCl2). Bacteria have then been collected by centrifugation and resuspended in a washing buffer (Tris 100 mM, glucose 10 mM). After centrifugation, the cell pellet has been dried at 70° C. overnight, weighted on a precision balance and dissolved in 5% nitric acid. Accumulated metal was measured by ICP-AES and the data are expressed as a function of the dry weight of the cell pellet.
Data from
M. gryphyswaldense MSR-1 strains have been cultivated in 1.5 L of lactate medium in the presence of cobalt (100 μM CoCl2). Bacteria have been then collected by centrifugation, and washed in the washing buffer. The cells have then been resuspended in 10 mL of resuspension buffer (HEPES 20 mM, NaCL 0.9% EDTA 1 mM glycerol 8%)+antiprotease and then disrupted by using a French press operating at 10.000 psi. 1 mL of the cell lysate has been kept for ICP-AES analysis of accumulated metals. The magnetosomes have been extracted from the rest of the lysate by simple magnetization, and washed 5 times with the resuspension buffer and then 5 times in using the same buffer except EDTA.
The final magnetosome resuspension has been eluted in 500 μL of an elution buffer (HEPES 20 mM glycerol 8%) and a fraction has been analyzed by ICP-AES. The content of cobalt in these magnetosomal preparations has been evaluated by comparison to the iron content.
Magnetosomes extracted from those samples have a cobalt to iron ratio of 1.05% in the control conditions, and 1.28% when using the pseudopaline producing strain. This corresponds to a 20% increase in cobalt accumulated inside the magnetosomes when the bacteria produce pseudopaline.
M. gryphyswaldense MSR-1 strains producing staphylopine have been cultivated in lactate medium in the presence of cobalt (100 μM CoCl2). Bacteria have been then collected by centrifugation, and washed in the washing buffer. The cells have then been resuspended in 10 mL of resuspension buffer (HEPES 20 mM, NaCL 0.9% EDTA 1 mM glycerol 8%)+antiprotease and then disrupted by using a French press operating at 10.000 psi. The magnetosomal fraction has been separated from the cytosolic fraction by simple magnetization, and washed 5 times with the resuspension buffer and then 5 times in using the same buffer except EDTA.
XANES spectra were recorded on biological samples (magnetosomal and cytosolic fractions prepared as described above) and on several cobalt containing references (Co(II)-acetylacetonate; Co(II)-glutathione; Co3O4, Co(II)-cysteine, Co(II)-nicotianamine, cobalamin (Vitamin B12), Co(II)-acetate, Co(II)-nitrate, Co(II)-phosphate and commercial CoFe2O4 pellets).
Data were collected at the Co K absorption edge (7.709 keV), by scanning in the energy range 7.65-7.90 keV (XANES) or 7.65-8.35 keV (EXAFS) with a nitrogen-cooled double crystal monochromator. Spectra were recorded in fluorescence mode, using the crystal analyzer spectrometer of CRG-FAME (BM30B) at ESRF operated in 7/8 bunches mode (200 mA). XANES spectra recorded on biological samples were analyzed by Linear combination fitting calculated using spectra of reference compounds.
Results presented in
a. Construction of the Plasmid for rpNxiA Expression
The vector used to express the permease was build using the pRK415 plasmid, as shown on
The mamGFDC promotor was subsequently cloned into prK415 using HindIII and BamHI (New England Biolabs ©) as restriction enzymes, resulting in the prK415-mam vector (
b. Resistance to Metal
The phenotypes associated with the presence of the permease and/or a metallophore were determined using recombinant M. gryphiswaldense MSR-1 cells cultivated in appropriated medium in the absence or presence of metals (100 μM cobalt or 1 mM nickel). The growth curves were obtained by following the OD each 2 hours during 48 H.
Data of
This result differs from the result obtained with metallophores which allow to increase both the accumulation of metal and the resistance.
c. Accumulation of Metal
In order to measure the quantity of cobalt accumulated, M. gryphiswaldense MSR-1 cells were incubated in the appropriate growth medium in the presence of 100 μM cobalt. After 24 H, cells were pelleted and washed (three times) using a washing buffer (Tris 100 mM glucose 10 mM pH 7.0). Cell pellets were then dried overnight and weighted before mineralization by addition of nitric acid (5%). Cobalt was subsequently quantified using ICP-AES.
| Number | Date | Country | Kind |
|---|---|---|---|
| 15306769.9 | Nov 2015 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2016/076856 | 11/7/2016 | WO | 00 |
