- Research article
- Open Access
Epsilon-Fe2O3 is a novel intermediate for magnetite biosynthesis in magnetotactic bacteria
Biomaterials Research volume 23, Article number: 13 (2019)
Natural biological magnetite nanoparticles are widely distributed from microorganisms to humans. It is found to be very important in organisms, especially in navigation. Moreover, purified magnetite nanoparticles also have potential applications in bioengineering and biomedicine. Magnetotactic bacteria (MTB) is considered one of the most abundant species around the world which can form intracellular membrane enveloped magnetic nanoparticles, referred to as magnetosomes. To our knowledge, the biomineralization of magnetosome in MTB involves a serious of genes located on a large unstable genomic region named magnetosome island, which specially exists in MTB. The magnetite core of magnetosome formed via a Fe (III) ion intermediates, for instance, α-Fe2O3 and ferrihydrite. Though the biosynthesis of magnetosome represents a general biomineralization mechanism of biogenic magnetite, knowledge of magnetosome biosynthesis and biomineralization remains very limited.
Cells used in this study were cultured in a 7.5-L bioreactor, samples for intermediate capture were taken each certain time interval after the generation of magnetosome biosynthesis condition. High-resolution transmission electron microscopy were used to analyze the detailed structure of magnetosomes. The parameters of the crystal structures were obtained by Fast Fourier Transform analyses.
In this study, we identified a novel intermediate phase, ε-Fe2O3, during the magnetite maturation process in MTB via kinetic analysis. Unlike α-Fe2O3, which has been reported as a precursor during magnetosome biosynthesis in MTB before, ε-Fe2O3, due to its thermal instability, is a rare phase with scarce natural abundance. This finding confirmed that ε-Fe2O3 is an important novel intermediate during the biomineralization of magnetosome in MTB, and shed new light on the magnetosome biosynthesis pathway.
Magnetite nano-particles are widely distributed mineral compounds found in various organisms including bacteria, bees, pigeons or even in human beings [1,2,3,4]. Membrane-enveloped magnetite, biosynthesized by magnetotactic bacteria (MTB), is referred to as magnetosomes [5, 6]. Although magnetosomes have great potential in bioengineering and biomedicine applications [7,8,9], the intracellular biomineralization mechanism of magnetosomes remains poorly understood. Since the discovery of MTB, it has been believed to be an optimal material for the study of biogenic magnetite biomineralization because of the simple structure of these organisms.
In most MTB, the magnetosomes are composed of magnetic magnetite (Fe3O4) or sulfide greigite (Fe3S4) [10, 11] enveloped by biological membrane . Under the action of a skeleton-like protein MamK and its binding partner MamJ, single magnetosome are arranged in chains parallel to the long axis of the cell [13,14,15].
Many studies using genetic, biochemical and physicochemical approaches have been performed to reveal the biological control of magnetosome synthesis in MTB. A series of genes were identified to be involved in this process, the mam genes, comprising the magnetosome island (MAI), which is a large unstable genomic region spanning 80–150 kb in length in different MTBs [16, 17]. However, knowledge about the chemical route of iron during the magnetosome formation process is limited and how iron ions are incorporated into magnetite is still a matter of debate. Previous studies using Mőssbauer spectroscopy suggested that ferrihydrite is a precursor for magnetite formation [18, 19]. This was further confirmed in Magnetospirillum gryphiswaldense MSR-1, a type strain for MTB study, using Fe K-edge X-ray absorption near edge structure (XANES) and high-resolution transmission electron microscopy (HRTEM) analysis . Real-time study about magnetosome biosynthesis using transmission electron microscopy (TEM) and X-ray absorption spectroscopy in MSR-1 revealed that full-sized magnetosomes formed within 15 min and immature magnetosomes contain a surface layer of hematite phase . In mamXY gene cluster mutants of MSR-1, distinct types of α-Fe2O3 particles co-existed with magnetite, hinting that the transformation of hematite phase to magnetite phase is a biocatalysis process . Magnetite formation from a phosphate-rich ferric hydroxide via nanometric ferric (oxyhydr) oxide intermediates was recently shown in Magnetospirillum magneticum AMB-1 . Together, these studies showed that the formation of magnetite in organisms possibly occured via Fe (III) ion intermediates and their oxides, hydroxides or oxyhydroxides.
It was suggested in the previous study that a thermal unstable phase of ferric oxide, ε-Fe2O3, was found in a mutant of MSR-1, which raised the possibility of a new type of intermediate during biomineralization process . In the present study, a kinetic analysis was performed to study the magnetosome maturation process from the early stage of its formation. The results showed that at each time point during maturation of magnetosomes after induction, magnetite co-existed with various iron-containing phases, including α-Fe2O3, ε-Fe2O3 and other undefined phases. This result indicated that mature magnetosomes form via different types of iron-containing intermediates, including some rare phases such as ε-Fe2O3.
Materials and methods
Bacteria and growth conditions
M. gryphiswaldense MSR-1 was cultured in SLM at 30 °C as described previously . The medium contained (per liter double distilled water) 2.5 g sodium lactate, 0.4 g NH4Cl, 0.1 g yeast extract, 0.5 g K2HPO4, 0.1 g MgSO4 • 7H2O, 0.05 g sodium thioglycolate and 5 mL trace element mixture. The strains were cultured at 30 °C in 250-mL serum bottles containing 100 mL medium with shaking at 100 rpm. Antibiotics nalidixic acid (Nx) was applied at 5 μg/mL for MSR-1.
Cell magnetic response curve of MSR-1 strain
The coefficient of magnetism (Cmag) value of MSR-1 was calculated from measurements of the maximal and minimal optical density (OD600) using a UV-visible spectrophotometer (UNICO2100; UNICO Instrument Co., Shanghai, China) .
Transmission electron microscope measurement
The structural details of the nanoparticles in MSR-1 samples from different time interval were analyzed by the HRTEM method using a JEM-2100F, which was operated at 200 kV, and it was equipped with a field emission gun, ultra-high-resolution pole piece, and ultrathin window JEOL detector. HRTEM images were obtained with an OSIS CANTEGA CCD camera. The crystals’ structural parameters were obtained by Fast Fourier Transform (FFT) analyses.
Time-course experiment for the detection of the intermediate phase at the early stage of magnetosome formation
MSR-1 cells were cultured in 5.0 L of SLM medium in a 7.5-L bioreactor as described previously , until the relative dissolved oxygen concentration (DO) decreased to 1%. Then, 30 mL of 10 mM ferric citrate was added to the culture to induce the synthesis of magnetosomes. Samples for HRTEM observation were collected at 0, 5, 10, 15 and 25 min after induction and fixed immediately with 2.5% glutaraldehyde. After washing three times with double-distilled water, the cells were dispersed onto a copper grid for HRTEM analysis.
For this study, in order to initiate the biomineralization of large amount of magnetite accurately, cultivation of M. gryphiswaldense MSR-1 was carried out in a 7.5-L bioreactor. After the relative dissolved oxygen decreased to 1%, ferric citrate was added to induce magnetosome biosynthesis, samples were taken at different time points and fixed in 2.5% glutaraldehyde to maintain their original state (Fig. 1). Then, cells were prepared for HRTEM analysis. From the result, even at the 0-min interval, the formation of several iron-containing nanoparticles was evident, though the size of the particles are very small. Then, the average diameter of magnetosomes grows with time passed (Fig. 2). During this time, the predominant phase composing the particles was magnetite, but other iron-containing phases, including α-Fe2O3 and ε-Fe2O3, were present (Fig. 3a and Fig. 4, the data of ε-Fe3O3 measured in this work and the theoretical data of ε-Fe2O3 and Fe3O4 (magnetite) are listed in Additional file 1: Table S1). The finding of α-Fe2O3 as an intermediate in magnetite biomineralization is in accordance with previously reports, but the existence of ε-Fe2O3, which is an unstable phase under normal conditions, has never been reported before. For this assay, a total of more than 400 particles were analyzed, and Fig. 5 shows the phase ratio of different iron species by induction time point, Fe3O4 (magnetite), ε-Fe2O3, and α-Fe2O3 (hematite) phases are denoted by subscripted M, ε, and H, respectively (Some of the data measured in this assay are listed in Additional file 1: Figure S1). At each induction time point before the formation of mature magnetosomes, iron oxides always co-exist and proportion of magnetite increased with time passed. This result indicates that various iron-containing precursors co-exist as intermediate phases at the initiation phase of magnetosome biomineralization. The HRTEM data are shown in Fig. 3a, Fig. 4 and the original images with high resolution are available in Additional file 1: Fig. S2. Other iron-containing phases will be discussed in detail in another paper.
Recent studies have confirmed the existence of α-Fe2O3 at the early stage of magnetosome formation and act as a precursor phase [20, 21, 23]. In this study, we discovered that a thermodynamically unstable iron oxide phase, ε-Fe2O3, co-existed with α-Fe2O3 at the early stage of magnetosome synthesis, thus demonstrating that both of these two iron oxide phases are intermediates during the maturation of magnetosomes.
α-Fe2O3, γ-Fe2O3, and Fe3O4 are the most frequent iron oxides present in bulk in nature (crystal structures of Fe3O4 and α-Fe2O3 are shown in Fig. 3b) . By contrast, ε-Fe2O3 is a rare phase with scarce natural abundance due to its thermal instability [29, 30]. Recently, the natural occurrence of a ε-Fe2O3 phase in some plants has been reported . The crystal structure of the ε-Fe2O3 phase is an orthorhombic non-centrosymmetric structure with Fe atoms occupying four distinct nonequivalent crystallographic sites, including one tetrahedral site and three different octahedral sites (Fig. 3b) . In the context of nano-materials, this structure is interesting, perhaps indicating a critical role of high surface energy, a characteristic of most nanostructures, in the formation of the epsilon phase with diameters of approximately 20 nm.
Similarities between the crystal structures of magnetite and ε-Fe2O3 are shown in Fig. 3b. Both tetrahedral and octahedral coordination of Fe and O occur in the two iron oxides; the stacking pattern of the two is formed by octahedral layers alternating with tetrahedral layers, with the exception of ordered octahedral vacancies in ε-Fe2O3. These similarities facilitate the structural transformation of ε-Fe2O3 to magnetite. Therefore, the formation of magnetite-containing magnetosomes via a ε-Fe2O3 intermediate may be more facile, even though α-Fe2O3 is more thermally stable.
The chemical synthesis of highly crystalline magnetite requires harsh conditions, and the ability of organisms to form such particles rapidly under moderate conditions remains an interesting question. Based on our current data and evidence from previous studies, a new chemical route model of magnetite biomineralization in MTB is proposed (Fig. 6): ferric ion is taken up into the cell and stored as a phosphate-rich ferric hydroxide phase . After dephosphorization, ferric ion is transferred to a magnetosome vesicle to form water- or hydroxyl-containing ferric oxide, followed by transformation into a variety of iron oxides that act as the precursors of mature magnetosomes, including Fe3O4, α-Fe2O3, ε-Fe2O3 and other phases that have not yet been defined. The mature magnetite crystals finally form from these intermediate phases.
Availability of data and materials
All data generated and analyzed in this study are available from the corresponding author on request.
Gould JL, Kirschvink JL, Deffeyes KS. Bees have magnetic remanence. Science. 1978;201(4360):1026–8.
Kirschvink JL, Kobayashi-Kirschvink A, Woodford BJ. Magnetite biomineralization in the human brain. Proc Natl Acad Sci U S A. 1992;89(16):7683–7.
Komeili A. Molecular mechanisms of magnetosome formation. Annu Rev Biochem. 2007;76:351–66.
Walcott C, Gould JL, Kirschvink JL. Pigeons have magnets. Science. 1979;205(4410):1027–9.
Blakemore RP. Magnetotactic bacteria. Annu Rev Microbiol. 1982;36:217–38.
Frankel RB, Blakemore RP, Wolfe RS. Magnetite in freshwater magnetotactic bacteria. Science. 1979;203(4387):1355–6.
Matsunaga NN. Highly sensitive detection of allergen using bacterial magnetic particles. Anal Chim Acta. 1993;281(3):585–9.
Alphandéry E, Faure S, Seksek O, Guyot F, Chebbi I. Chains of magnetosomes extracted from AMB-1 magnetotactic bacteria for application in alternative magnetic field cancer therapy. ACS Nano. 2011;5(8):6279–96.
Borg S, Hofmann J, Pollithy A, Lang C, Schüler D. New vectors for chromosomal integration enable high-level constitutive or inducible magnetosome expression of fusion proteins in Magnetospirillum gryphiswaldense. Appl Environ Microbiol. 2014;80(8):2609–16.
Bazylinski DA, Frankel RB, Heywood BR, Mann S, King JW, Donaghay PL, Hanson AK. Controlled biomineralization of magnetite (Fe3O4) and greigite (Fe3S4) in a magnetotactic bacterium. Appl Environ Microbiol. 1995;61(9):3232–9.
Pósfai M, Lefèvre CT, Trubitsyn D, Bazylinski DA, Frankel RB. Phylogenetic significance of composition and crystal morphology of magnetosome minerals. Front Microbiol. 2013;4(4):344.
Jogler C, Schüler D. Genomics, genetics, and cell biology of magnetosome formation. Annu Rev Microbiol. 2009;63:501–21.
Scheffel A, Gruska M, Faivre D, Linaroudis A, Plitzko JM, Schüler D. An acidic protein aligns magnetosomes along a filamentous structure in magnetotactic bacteria. Nature. 2006;440(7080):110–4.
Komeili A, Li Z, Newman DK, Jensen GJ. Magnetosomes are cell membrane invaginations organized by the actin-like protein MamK. Science. 2006;311(5758):242–5.
Pradel N, Santini CL, Bernadac A, Fukumori Y, Wu LF. Biogenesis of actin-like bacterial cytoskeletal filaments destined for positioning prokaryotic magnetic organelles. Proc Natl Acad Sci U S A. 2006;103(46):17485–9.
Grünberg K, Müller EC, Otto A, Reszka R, Linder D, Kube M, Reinhardt R, Schüler D. Biochemical and proteomic analysis of the magnetosome membrane in Magnetospirillum gryphiswaldense. Appl Environ Microbiol. 2004;70(2):1040–50.
Murat D, Quinlan A, Vali H, Komeili A. Comprehensive genetic dissection of the magnetosome gene island reveals the step-wise assembly of a prokaryotic organelle. Proc Natl Acad Sci U S A. 2010;107(12):5593–8.
Faivre D, Böttger LH, Matzanke BF, Schüler D. Intracellular magnetite biomineralization in bacteria proceeds by a distinct pathway involving membrane-bound ferritin and an iron (II) species. Angew Chem Int Ed Engl. 2007;46(44):8495–9.
Frankel RB, Blakemore RP. Magnetite and magnetotaxis in microorganisms. Bioelectromagnetics. 1989;10(3):223–37.
Fdez-Gubieda ML, Muela A, Alonso J, Garcia-Prieto A, Olivi L, Fernandez-Pacheco R, Barandiaran JM. Magnetite biomineralization in Magnetospirillum gryphiswaldense: time-resolved magnetic and structural studies. ACS Nano. 2013;7(4):3297–305.
Staniland S, Ward B, Harrison A, Laan GVD, Telling N. Rapid magnetosome formation shown by real-time x-ray magnetic circular dichroism. Proc Natl Acad Sci U S A. 2007;104(49):19524–8.
Raschdorf O, Müller FD, Pósfai M, Plitzko JM, Schüler D. The magnetosome proteins MamX, MamZ and MamH are involved in redox control of magnetite biomineralization in Magnetospirillum gryphiswaldense. Mol Microbiol. 2013;89(5):872–86.
Baumgartner J, Morin G, Menguy N, Perez Gonzalez T, Widdrat M, Cosmidis J, Faivre D. Magnetotactic bacteria form magnetite from a phosphate-rich ferric hydroxide via nanometric ferric (oxyhydr) oxide intermediates. Proc Natl Acad Sci U S A. 2013;110(37):14883–8.
Zhang Y, Wen T, Guo F, Geng Y, Liu J, Peng T, Guan G, Tian J, Li Y, Li J, et al. The disruption of an OxyR-like protein impairs intracellular magnetite biomineralization in Magnetospirillum gryphiswaldense MSR-1. Front Microbiol. 2017;08:208.
Guo FF, Yang W, Jiang W, Geng S, Peng T, Li JL. Magnetosomes eliminate intracellular reactive oxygen species in Magnetospirillum gryphiswaldense MSR-1. Environ Microbiol. 2012;14(7):1722–9.
Zhao L, Dan W, Wu LF, Tao S. A simple and accurate method for quantification of magnetosomes in magnetotactic bacteria by common spectrophotometer. J Biochem Biophys Methods. 2007;70(3):377–83.
Liu Y, Li GR, Guo FF, Jiang W, Li Y, Li LJ. Large-scale production of magnetosomes by chemostat culture of Magnetospirillum gryphiswaldense at high cell density. Microb Cell Factories. 2010;9:99.
Bursill LA, Withers RL. On the multiple orientation relationships between hematite and magnetite. J Appl Crystallogr. 1979;12(3):287–94.
Forestier H, Guiot-Guillain G. Ferromagnetic variety of Fe2O3. C R Académie des Sciences. 1934;199:720.
Tronc E, Chanéac C, Jolivet JP. Structural and magnetic characterization of ε-Fe2O3. J Solid State Chem. 1998;39:93–104.
McClean RG, Kean WF, Dick T, Gajdardziska-Josifovska M. Botanical iron minerals correlation between nanocrystal structure and modes of biological self-assembly. Eur J Mineral. 2001;13(6):1235–42.
Kelm K, Mader W. Synthesis and structural analysis of ε-Fe2O3. Z Anorg Allg Chem. 2005;631(12):2383–9.
This work was supported by The Project for Extramural Scientists of State Key Laboratory of Agrobiotechnology (Grant No. 2015SKLAB6–21) and National Natural Science Foundation of China (Grant Nos. 31570067, 31170089, 31270093, 31860013 and 21201012).
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Figure S1. HRTEM images with high resolution and the corresponding FFT analyses of intracellular iron oxide nanoparticles in MSR-1 wild type after the induction of ferric citrate for different time interval. Figure S2. Some representative HRTEM images of epsilon-Fe2O3 and alpha-Fe2O3 used for the phase ratio determination in Fig. 5 of the main text. Table S1. Crystallographic information of the ε-Fe2O3 exhibited in Fig. 3a, Fig. 4 and the theoretical data of ε-Fe2O3 and Fe3O4 (magnetite). For further crystallographic information, people can refer to pdf card as 33–0664 for α-Fe2O3, 65–3107 for magnetite and 52–1449 for ε-Fe2O3, respectively. (DOCX 19846 kb)