Moonlighting Arabidopsis molybdate transporter 2 family and GSH

Communications Biology volume 6, Article number: 801 (2023) Cite this article

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Molybdenum (Mo) as essential micronutrient for plants, acts as active component of molybdenum cofactor (Moco). Core metabolic processes like nitrate assimilation or abscisic-acid biosynthesis rely on Moco-dependent enzymes. Although a family of molybdate transport proteins (MOT1) is known to date in Arabidopsis, molybdate homeostasis remained unclear. Here we report a second family of molybdate transporters (MOT2) playing key roles in molybdate distribution and usage. KO phenotype-analyses, cellular and organ-specific localization, and connection to Moco-biosynthesis enzymes via protein-protein interaction suggest involvement in cellular import of molybdate in leaves and reproductive organs. Furthermore, we detected a glutathione-molybdate complex, which reveals how vacuolar storage is maintained. A putative Golgi S-adenosyl-methionine transport function was reported recently for the MOT2-family. Here, we propose a moonlighting function, since clear evidence of molybdate transport was found in a yeast-system. Our characterization of the MOT2-family and the detection of a glutathione-molybdate complex unveil the plant-wide way of molybdate.

Moco-biosynthesis is crucial for the functionality of Moco-dependent enzymes (Moco-enzymes), key elements of basic metabolic pathways in planta1. The four-step process involves six enzymes and is conserved throughout all kingdoms of life2. Molybdate insertion into molybdopterin is maintained by molybdenum-insertase Cnx1 (Cofactor for nitrate reductase and xanthine dehydrogenase 1) acting in a multi-enzyme complex3. The Moco key user nitrate reductase (NR) catalyzes the first step of nitrate assimilation4. Moco-enzymes are, inter alia, involved in abscisic acid (ABA) biosynthesis by the abscisic aldehyde oxidase (AAO)5 and sulfite detoxification by the sulfite oxidase6.

Efficient absorption of molybdate (MoO42-) and distribution from soil into cells is essential for Moco-biosynthesis in plants and is maintained by specialized molybdate transporter (MOT) proteins7. Two independent MOT families are thought to exist8,9, however, only members of the MOT1-family have been characterized to date, playing distinct physiological roles in Moco-biosynthesis7.

MOT1.1 (formerly known as MOT17; AT2G25680) is a plasma membrane (PM) protein with a high-affinity molybdate transport activity (Km of 20 nM)10 and is most prominently produced in roots11. Therefore, MOT1.1 functions as radicular molybdate importer from soil but is not involved in leaf cell import or in molybdate delivery to the Moco-biosynthesis complex7. The highly-related, tonoplast-localized MOT1.2 (formerly known as MOT27; AT1G80310)12 is the second member of the MOT1-family. It controls the release of stored molybdate from the vacuole by direct interaction with Cnx17.

Despite the reported functions of MOT1-family members, two mechanisms remained unclear to fully understand molybdate homeostasis in plants: (i) how molybdate enters leaf and seed cells and (ii) how it is imported into the vacuole. It is conceivable that members of the second MOT-family might maintain these tasks.

The independent and unrelated MOT2-family was first discovered in Chlamydomonas reinhardtii8. CrMOT2 showed high-affinity molybdate uptake activity (Km of 550 nM) when heterologously produced in yeast. Orthologues of genes are present in most eukaryotes, including animals8 and higher plants like Oryza sativa13. Even though the presence of three MOT2-family members in Arabidopsis thaliana (A. thaliana) were postulated8,9, as to yet, a MOT function for this family has not been proven9,14.

Recently, Arabidopsis MOT2-family was associated with an additional putative S-adenosyl methionine (SAM) Golgi import function for polysaccharide methylation, necessary for correct cell wall biosynthesis14.

Here we report the identification of four members of the MOT2-family in A. thaliana and show their molybdate transport activity. PM-localization and interaction with molybdenum-insertase Cnx1 reveal their role as molybdate importers. Due to the additional function as Golgi-SAM importers, we postulate a moonlighting character. Our findings of global expression of one MOT2-family member and its importance for Moco key-user NR show its pivotal role in molybdate distribution and cellular import to directly supply Moco-biosynthesis. Remaining MOT2-family members are produced in flowers and a role in seed and pollen maturation is suggested. We detected a glutathione-molybdate complex, which shows how vacuolar storage of molybdate is functioning. Altogether, our findings outline the plant-wide way of molybdate from uptake, distribution, storage, and usage in Moco-biosynthesis.

Two MOT-families are present in Chlamydomonas reinhardtii consisting of one member each: CrMOT115 and CrMOT28. According to its homology to CrMOT2 the protein AtMOT2.1 of A. thaliana encoded by gene AT4G277208 was identified. The encoded proteins CrMOT2 and AtMOT2.1 share an amino acid (aa) similarity of 71% and contain four highly conserved motifs8 characteristic for MOT2 proteins (Fig. 1a). In a phylogenetic analysis, Huang et al.9 identified two more mot2-related genes in A. thaliana: Atmot2.2 (AT1G64650) and Atmot2.3 (AT3G49310). Analyses of the encoded proteins revealed a sequence similarity of over 83% on aa level, showed their association to the major facilitator superfamily, and, most importantly, identified four MOT2 specific motifs (Fig. 1a). mot2.2 encodes for two proteins: MOT2.2 A consists of 462 aa and its splice variant MOT2.2B which lacks the first 41 aa. MOT2.3 consists of 460 aa.

a ClustalW alignment of MOT2 sequences from Chlamydomonas reinhardtii (Cr) and A. thaliana (At). Identical aa are marked in dark grey, similar in light grey and different in white. Four highly conserved domains are marked with red boxes. b Representative growth curve of Moco-yeasts in molybdate-chlorate medium with induced (black; +Gal) and non-induced (grey; –Gal) mot1.1 expression. Biomass index of 40 RLU is marked with a red dotted line. c Time in hours to reach a biomass index of 40 RLU of Moco-yeasts with induced (black; +Gal) and non-induced (white, –Gal) mot expression. Mean of two independent experiments is plotted and error bars depict standard deviation. Unpaired T-test was used to test for significance. **P ≤ 0.01; ***P ≤ 0.001. d Ranking according the time to reach biomass index of 40 RLU of Moco-yeasts with induced mot expression as indicated. Growth behaviour was normalized to chlorate-free controls. Quantitative data in Fig. 1c was additionally analyzed by two-way ANOVA and Sidak post hoc test for multiple comparison (Table S2).

Molybdate transport function of the MOT2-family was tested by an in vivo yeast-based growth assay. Wild type (WT) Saccharomyces cerevisiae lacks genes connected to molybdenum metabolism, including MOTs16. Fungal genes encoding the Moco-biosynthesis and NR derived from Neurospora crassa were integrated into the yeast genome (Table S1) following the approach of Perli et al.17, and both Moco-biosynthesis as well as NR-activity were detected when co-expression of mot candidate genes was induced in growth media containing a physiological amount of 100 nM molybdate.

As next step, an in vivo-growth assay with the Moco-yeast strains was performed. NR not only reduces nitrate to nitrite but also chlorate to cytotoxic chlorite18,19. When co-expressed mot candidates are capable of active molybdate transport, Moco-yeasts become more sensitive towards chlorate due to functional Moco-biosynthesis which yields active NR capable of producing cytotoxic chlorite. Resulting growth inhibition can be quantified using a BioLector® growth analyzer.

Moco-yeasts expressing mot1.1 as positive control (Fig. 1b) showed significantly impaired growth in presence of chlorate and molybdate when gene expression was induced by galactose. Analyses of mot1.2 and all mot2 candidates (Fig. 1c) revealed significant growth inhibition after galactose induction comparable to the positive control. Thus, induced expression of all tested mot2 candidates caused a molybdate transport dependent growth inhibition based on the production of cytotoxic chlorite due to an increased NR-activity. Furthermore, an apparent order of molybdate transport capacity was observed (Fig. 1d). MOT1.1 and MOT1.2 showed the highest capacity, followed by MOT2.3, MOT2.2B, MOT2.2 A, and MOT2.1.

Intracellular localization of MOT2 was elucidated by fluorescence microscopy in Nicotiana benthamiana (N. benthamiana) mesophyll protoplasts. All N-terminally fused Venus-MOT2 constructs showed no or only weak signals. Consequently, only C-terminally fused MOT2-Venus constructs were analyzed. All MOT2-family members localized similarly as a thin layer encircling the protoplast at its periphery (Fig. 2). Co-expression with the cytosol marker eqFP611 (Fig. 2a1–d1) showed clear differentiation of the signals whereas co-localization with the PM-marker AtPIP2A20 (Fig. 2a2–d2) was observed indicating PM-localization of MOT2. In addition, fluorescence was detected in vesicle like structures. An additional localization experiment in A. thaliana seedlings verified PM-localization and showed co-localization with the cis-Golgi marker GmMan-121 (Fig. S2).

a–d Transient chemical transformation of N. benthamiana mesophyll protoplasts with MOT2-Venus fusion constructs and co-expression of eqFP611 as cytosolic marker (a1–d1) or AtTPIP2A-RFP as PM-marker (a2–d2). Images are merge of Venus (yellow), chloroplast auto-fluorescence (red) and marker (eqFP611 in blue, a1-d1; AtPIP2A-RFP in cyan, a2–d2) detection channels. A splitted image, showing each fluorescence channel individually can be found in Fig. S1. e–l Split-10 + 1 GFP topology studies by Agrobacterium-mediated transient transformation of N. benthamiana leaves with GFP11-MOT2 (e, g, i and k) and MOT2-GFP11 (f, h, j and l). Co-transformation after 2 days with cytosolic GFP-10 (e1-l1) or apoplastic SP-GFP1-10 (e2-l2). Images are merge of GFP (green) and chloroplast auto-fluorescence (red) detection channels. Images were taken after 2-3 days using a C-Apochromat 40x/1.2 water immersion objective (a–d) or a Plan-Neofluar 10x/0.3 objective (e–l). Scale bars depict 20 μm.

Topology studies were performed to determine N- and C-terminus orientation using a split-GFP system in N. benthamiana leaf epidermis cells22. MOT2 proteins were tagged N- (Fig. 2e1 + 2, 2g1 + 2, 2i1 + 2 and 2k1 + 2) or C-terminally (Fig. 2f1 + 2, 2h1 + 2, 2j1 + 2 and 2l1 + 2) with the 11th β sheet of GFP (GFP11) and were co-expressed with either a cytosolic GFP1-10 or with GFP1-10 tagged with an apoplast signal peptide (SP-GFP1-10). All MOT2-family members tagged N-terminally with GFP11 (GFP-11-MOT2) showed a fluorescence signal after reporter reconstitution with the apoplastic SP-GFP1-10 (Fig. 2e2, g2, i2 and k2). Fluorescence was also detected after all C-terminally GFP-11-tagged MOT2-family members (MOT2-GFP11) interacted with cytosolic GFP1-10 (Fig. 2f1, h1, j1 and l1). Consequently, the N-terminus of all MOT2 proteins is oriented into the apoplast, whereas the C-terminus is oriented into the cytosol further underlining their PM-localization.

To assign a physiological role to MOT2-family members their spatial and temporal organ-specific expression patterns were studied. Histochemical analysis of mot2.1:gus plants (Fig. 3a–e) showed signals in roots concentrated in vascular tissue. Expression was also detected in epidermis and vascular tissue of shoots and in developing flowers with strong signals in ovaries. Young leaves showed global expression reduced to main leaf venation with increasing age (Fig. 3b, c) as also quantified by fluorimetric assay (Fig.3f). Interestingly, the fluorimetric assay also revealed a significant increase of mot2.1 expression under molybdate abundance in all organs except the flower. mot2.2:gus plants showed very distinct signals in pollen grains of mature flowers (Fig. 3g). Analysis of mot2.3:gus showed signals in ovaries (Fig. 3h). Availability of molybdate had no influence on expression patterns of mot2.2:gus and mot2.3:gus. Expression of mot2.2 and mot2.3 in the flower did not allow a fluorimetric analysis.

a–e Histochemical GUS assay of mot2.1:gus Arabidopsis plants. Depicted are root (a), old leaf (b), young leaf (c), shoot cross-section (d) and ovary (e). f Fluorimetric GUS assay of mot2.1.gus plants. Plotted is the mean of 7-10 plants of three independent lines for both conditions. Each organ was analyzed as technical triplicate. Error bars depict standard deviation. Unpaired t-test was used to test for significance. ns = not significant, *P ≤ 0.05, **P ≤ 0.01. g Histochemical assay of mot2.2:gus flower. h Histochemical assay of mot2.3:gus flower. WT shows no background activity (Fig. S3). Images 3a, b, c, e, g and h are identical to the respective images in Supplementary Fig. S3. Scale bars depict 500–2000 µm as indicated for each panel. Plants for histochemical assay were grown hydroponically under +Mo conditions and for fluorimetric assays under +Mo and -Mo conditions. Quantitative data in f was additionally analyzed by two-way ANOVA and Sidak post hoc test for multiple comparison (Table S3).

Molybdate deprivation has a striking effect on plants and leads to reduced activity of Moco-enzymes resulting in retarded growth, leaf necrosis, dwarfism, and ultimately death23. Loss of MOTs can cause this phenotype under molybdate shortage, as demonstrated for members of the MOT1-family7. Phenotype of Arabidopsis mot2 T-DNA knockout (KO) lines (Table 1) were analyzed to reveal whether the loss of MOT2-family members impacts vegetative growth and molybdate homeostasis. The interplay between members of the MOT1- and the MOT2-family in maintaining molybdate homeostasis was analyzed by characterizing KO lines with a higher degree in comparison to WT and a mot1.1 single-KO, encoding the main root molybdate importer MOT1.1, regarding their impact on vegetative growth. A loss of the vacuolar exporter MOT1.2 showed no effects neither on the macroscopic nor the molecular phenotype as observed in a recent study7. Due to the organ-specific expression patterns of mot2.2 and mot2.3 (Fig. 3g, h; Fig. S3), both were excluded from higher degree KO analyses.

Interestingly, no notable alterations in plant survival, development (Fig. S4) or growth behavior were observed (Fig. 4a–c). As MOT2.1 is primarily present in root vascular tissue (Fig. 3a), a molybdate uptake assay was performed to test whether uptake is impaired in mot2.1-KO plants (Fig. 4d). Whereas molybdate uptake rate of the positive control mot1.1-KO was significantly decreased compared to WT, mot2.1-KO showed only a minor reduction. NR-activity is directly linked to Moco availability and, thus, an important indicator to show functionality of molybdate supply. Molybdate deprivation reduced NR-activity in the WT (Fig. 4e) significantly from 0.47 nmol ∙ (h ∙ mgFW)−1 by 32% to 0.32 nmol ∙ (h ∙ mgFW)−1. Comparable results were observed for mot2.2-KO and mot2.3-KO. Interestingly, mot2.1-KO showed a significant reduction of NR activity by 30 % under both, molybdate availability and deprivation conditions.

Arabidopsis mot2-KOs were grown under molybdate availability (+/+Mo) and deprivation (–/–Mo) in a hydroponic system for 85 days. a Fresh weight of rosette leaves. b Root length. c Leaf area growth curve within 85 days. Plotted is the mean of 8–15 individuals. d Molybdate uptake rate normalized to leaf area of WT, mot1.1-KO and mot2.1-KO of 56 days old plants. Plotted is the mean of 6–9 individuals for controls and 26 individuals of the mot2.1-KO. Quantitative Data was additionally analyzed by one-way ANOVA and Dunnet post hoc test for multiple comparison (Table S4). e NR-activity of mot2-KOs grown hydroponically for 60 days. Plotted is the mean of 8–15 individuals. Error bars depict standard deviation. Unpaired T-test was used for significance tests. ns = not significant, *P ≤ 0.05, **P ≤ 0.01. Quantitative data was additionally analyzed by two-way ANOVA and Tukey post hoc test for multiple comparison (Table S5).

The mot1.1 mot2.1 double KO (dKO) and a mot1.1 mot1.2 mot2.1 triple KO (tKO) showed only slight alterations when grown hydroponically under molybdate deprivation in fresh weight, leaf area production and root length (Fig. S5a–c) compared to molybdate availability. Under the same conditions the mot1.1 showed a significant reduction of leaf area production as observed recently7. Interestingly, the a mot1.1 mot1.2 mot2.1 tKO showed a plant survival that was significantly reduced by 45 % compared to control conditions (Fig. S5d). The observed significant reduction in NR activity in the mot1.1 mot2.1 dKO (Fig. S5e) was comparable to that of the mot1.1 KO under molybdate deprivation as already described earlier7. Interestingly, the mot1.1 mot1.2 mot2.1 tKO showed a drastically reduced NR activity even under molybdate availability conditions that was further decreased significantly under molybdate deprivation.

Cytosolic Moco-biosynthesis proteins undergo tight protein-protein interactions in a multi-protein complex anchored to actin by Cnx124. Additionally, Cnx1 is supplied with molybdate from the vacuole by interaction with MOT1.27. Therefore, a direct supply of Cnx1 with extracellular molybdate by protein-protein interaction with the MOT2-family was investigated by bimolecular fluorescence complementation (BiFC).

Here, only a C-terminal reporter fusion to MOT2-family members was taken into consideration as topology studies revealed that only the C-terminus is oriented into the cytosol. Aquaporin AtPIP2A is PM-localized20 and served as negative control. MOT2.1-VYNE co-expressed with Cnx1-SCYCE showed brighter fluorescence intensity (Fig. 5a1) than the negative control (Fig. 5a2). Abundance controls (Fig. S6) displayed comparable fluorescence intensities indicating that MOT2.1 and AtPIP2A were present in equal amounts. Results demonstrate interaction of MOT2.1 with Cnx1. Analysis of MOT2.1 and Cnx1 by split-luciferase (split-LUC) experiments underline this interaction and designate the G-domain of Cnx1 as main interaction partner (Fig. S7). BiFC interaction approaches of MOT2.2A (Fig. 5b1) and MOT2.3 (Fig. 5d1) showed higher fluorescence intensities compared to the respective negative controls demonstrating interactions with Cnx1 (Fig. 5b2, d2). Solely the shorter MOT2.2B showed no interaction with Cnx1 (compare Fig. 5c1, c2).

a1–d1 Interaction approaches with transiently transformed leaves of N. benthamiana co-expressing MOT2-VYNE and Cnx1-SCYCE. a2–d2 Negative controls with AtPIP2A-VYNE. Images depict the lower leaf epidermis cell layer and were taken with a Plan-Neofluar 10x/0.3. Scale bars depict 20 μm. Abundance controls, where CLuc replaces Cnx1, showed comparable fluorescence intensities of the proteins of interest and the negative control to display artefacts derived from random interaction (Fig. S6).

Until now it remained unclear how molybdate is imported into the vacuole. Since no member of the MOT2-family was localized in the tonoplast an independent mechanism is suggested. Therefore, we hypothesized complex formation of glutathione (GSH) and the heavy metal (HM) ion molybdate. In general, HMs (e.g. cadmium) are nonspecifically sequestered by GSH, channeled into the vacuole and released25.

Complex formation of GSH with cadmium ions induces charge transfer of sulfhydryl groups showing absorption in the far ultra-violet (UV) spectral region26. To study if such an effect could account for molybdate sequestration, equimolar concentrations of GSH and molybdate were co-incubated and analyzed by spectroscopy (Fig. 6a). After subtraction of the molybdate background, a bathochrome shift from λmax = 221 nm to λmax = 261 nm and an increased peak intensity were observed when both components were mixed giving a first indication of GSH-molybdate complexes.

a UV spectra of GSH and GSH with molybdate. b HRMS spectra of GSH, molybdate and a GSH-molybdate mixture recorded in negative mode. Shown are absolute ion intensities in the range of m/z = 420–445. No dominant ions are present in the GSH sample. Unassigned ions in the molybdate MS possibly originate from poly-molybdates. The solution containing both molybdate and GSH shows new ions that are not present in the stock solutions containing solely GSH or molybdate. Comparison with calculated isotopic pattern of a GSH-molybdate complex sum formula C10H14MoN3O8S-. c MS2 fragmentation of C10H14MoN3O8S- with 25 normalized collision energy. Experimentally observed fragment masses were in agreement with calculated ones (Panel d). d Proposed fragmentation of a molybdate chelate complex with bidentate GSH, matching the ions observed ions observed in MS2 experiments (Panel c). Listed are exact masses and respective sum formulas.

The presence of GSH-molybdate complexes was verified by high-resolution mass spectrometry (HRMS). Mixed solutions of GSH and molybdate show an ion that is not present in pure solutions of both components. The new ion ([M-H+] = 433.9561) was assigned the molecular formula C10H14MoN3O8S- (Fig. 6b), indicating the formation of a chelate complex with bidentate GSH and molybdate under the elimination of water. This complex formed reproducibly under different molar ratios of GSH and molybdate (1:1 to 9:1) and various pH values (pH = 3–9). Observed isotopic pattern is in agreement with calculated isotopic ratio for a GSH-molybdate complex (Fig. 6b). The ambidentate character of GSH allows several types of molybdate complexation. Thus, the corresponding ion (m/z = 433.9561) was analyzed by tandem mass spectrometry (MS2) at different collision energies to decipher its structure (Fig. 6c). Use of isotopically enriched (98MoO42-) simplified the MS2 spectra, which showed the loss of a fragment consistent with C5H7NO3. This fragment was assigned as glutamine (Fig. 6d), indicating that molybdate is complexed by glycine and cysteine. Accordingly, a fragment corresponding to HMoO3S- supported the complexation of cysteine by sulfur (Fig. 6c, d). These HRMS experiments suggest that GSH acts as bidentate ligand, chelating molybdate via the carboxylate of glycine and the thiol in cysteine.

Molybdate is a crucial micronutrient for plants and acts as active component of Moco, on which activity of important Moco-enzymes is relying. Molybdate uptake is maintained by specialized MOT proteins. Whereas the physiology of the MOT1-family in Arabidopsis is well understood7, global molybdate homeostasis remained unclear until now. The presence of a MOT2-family in A. thaliana was repeatedly postulated, however, their MOT function has never been experimentally proven so far. By in silico studies, three mot2-genes encoding four MOT2-proteins with high sequence similarity to the characterized CrMOT2 were identified8,9. All of the encoded proteins share four highly conserved motifs essential for molybdate transport8. All four MOT candidates imported molybdate into yeast cells with lower capacity than MOT1.1 which has been characterized as high-affinity importer10. Furthermore, all MOT2s are localized in the PM. Therefore, MOT2-family members generally maintain molybdate import from extracellular space into cytosol. However, their individual organ-specific expression pattern suggests versatile physiological functions, complementing the MOT1-family.

Recently it was shown that loss of the main radicular molybdate importer MOT1.1 led to dwarfism and dramatically reduced NR-activity under molybdate shortage caused by a reduced molybdate uptake7. Observed expression of mot2.1 in roots could indicate a supportive role in molybdate uptake. However, loss of MOT2.1 has no impact on molybdate uptake from soil, which points to a different function after molybdate has been taken up by MOT1.1. MOT2.1 might rather be responsible for molybdate distribution within the plant as well as delivery of molybdate to Moco-biosynthesis. This model is supported by a strong expression of mot2.1 in young leaf tissue, shoot vascular tissue and main leaf venation that is induced by presence of molybdate, by its PM-localization, and by its direct protein interaction with molybdenum-insertase Cnx1. Loss of MOT2.1 affected efficiency of Moco-biosynthesis due to reduced supply with molybdate, observed by reduction of NR-activity. In contrast, lack of MOT2.2 A, MOT2.2B, and MOT2.3 had neither an effect on vegetative growth nor on NR-activity. This leads to the conclusion that, even though, an interaction of MOT2.2 A and MOT2.3 with Cnx1 was detected, they only play minor roles in Moco-biosynthesis supply.

Strikingly, all members of the MOT2-family are expressed in the flower. Both, mot2.1 and mot2.3, are highly expressed in ovaries where import of essential nutrients into developing seeds takes place. Taken their organ-specific expression into account, one can assume an involvement in loading molybdate into developing seeds.

In addition of making molybdate available for the daughter generation, high amounts of molybdate in developing seeds might fulfil two additional roles. First, the Moco-enzyme AAO catalyzes the last step of ABA biosynthesis which is the key-hormone in promoting seed dormancy5. Although the majority of ABA originates from vegetative tissue and is transported to the seed, ABA is also produced in seed coating tissues27. This demand of molybdate for functional Moco can be met by MOT activity. Secondly, high molybdate concentrations (>250 µM) in reproductive organs might be necessary with regard to their inhibitory effect on purple acid phosphatases (PAP)28. The main storage form of phosphor in seeds and pollen grains is phytic acid. One member of PAPs, AtPAP15, is localized in pollen grains and is thought to be the key-phytase during pollen germination to mobilize phosphorous reserves28. A genome wide analysis of pap genes in Brassica rapa revealed potential functions of several PAPs in pollen maturation, germination, and pollen tube elongation29. Therefore, it can be assumed that molybdate acts as key-inhibitor on PAPs to avoid premature pollen maturation and germination. Expression of mot2.2 in pollen grains suggests involvement in this important process.

Elucidation of the physiological roles of the MOT2-family gives a broad insight into molybdate homeostasis. The radicular importer MOT1.1 absorbs molybdate from soil with a strikingly high-affinity7,10. In younger plants, MOT2.1 is involved in plant wide distribution, cellular import, and supply of Moco-biosynthesis with molybdate via direct interaction with Cnx1. Previous studies revealed that the vacuole serves as main storage12 from where molybdate is exported by MOT1.2 and handed over to Cnx1 for Moco-biosynthesis7. A perturbation of this interplay, interestingly, has a severe effect on vegetative growth. The simultaneous loss of the main radicular importer MOT1.1, the main cellular importer MOT2.1, and the tonoplast exporter MOT1.2 showed a drastic reduction in NR activity culminating in a strongly reduced plant survival rate independent of molybdate presence.

Since free molybdate as HM-ion has a hazardous potential25, the route of molybdate throughout the plant raises an interesting question: How is molybdate imported into the vacuole after cellular import? One general coping mechanism is the conjugation of HM-ions with GSH mediated by GSH-S-Transferases30. The conjugate is imported to the vacuole and dissociates due to pH shifts25. Therefore, we hypothesize that excess molybdate is sequestered by GSH to avoid toxic processes. This model was supported by a bathochrome shift in absorption caused by formation of GSH/molybdate-complexes as shown for several HM/GSH-complexes26,31 and additionally evidenced by mass spectrometry experiments. These results support a model in which molybdate is channelled in conjugation with GSH into the vacuole by unspecific HM/GSH transporters32. There, the complex dissociated due to the pH shift so that molybdate can be stored and exported by MOT1.2 when needed for Moco-biosynthesis. All MOT2-family members are expressed in the reproductive organs to import molybdate. Both splice variants of MOT2.2, thereby, might fulfil different roles: While MOT2.2 A directly interacts with Moco-biosynthesis to supply AAO, MOT2.2B is not interacting with Moco-biosynthesis and might supply free molybdate for PAP inhibition and seed nutrition storage.

Recently, MOT2-family proteins were implicated as SAM-transporters located in the Golgi14. In this study, the double KO of mot2.1 (GoSAMT2) and mot2.2 (GoSAMT1) showed reduced Golgi synthesized polysaccharide methylation and changed cell wall architecture. Furthermore, fluorescence signals of MOT2-GFP co-localized with the GFP-tagged Golgi marker GmMan-1. Results of the present study confirmed Golgi localization of all MOT2-family proteins but also showed their clear PM-localization and, most importantly, molybdate transport activity. Given their different localization and different substrates one can assume moonlighting character for the MOT2-family by fulfilling more than only one function33. Activity of MOT2-family proteins in Golgi and PM is likely, since the Golgi is a station of MOT2-family members on their way to their final destination, the PM34. Also for other members of Moco-metabolism moonlighting activity was demonstrated35. For example, gephyrin, the human homologue of Cnx1, is involved neuronal transporter/microtubule interaction36, while Moco binding proteins are also involved in cytokinin-biosynthesis37. Therefore, the moonlighting transporters of the MOT2-family are of pivotal importance for SAM-import into Golgi and plant wide molybdate homeostasis

Molybdate transport activities of MOT2 candidates were tested in yeast. As baker’s yeast Saccharomyces cerevisiae has lost molybdenum metabolism during evolution and hence harbors no Moco-enzymes16 it is a suitable model organism to test for molybdate transport, as described in detail in Table S1.

N. benthamiana WT plants were used for localization, topology and BiFC analysis. WT A. thaliana Col-0 ecotype was used to generate stable transgenic lines carrying endogenous mot2:gfp-gus constructs and as control plants. A. thaliana T-DNA insertion KO lines (Table 1) were maintained from NASC (Nottingham, UK). Presence of T-DNA insertion at correct loci and homozygotic status of used KO lines were verified with genotyping PCRs. Higher degree KOs were generated by manually crossing of single KO lines. The status of molybdate availability between lines purchased from NASC and of that generated by manually crossing could not be validated.

Atmot2.1 was identified according to Tejada-Jiménez8 using TAIR38. Analysis of mot2.1 with EnsmblPlants39 revealed two highly-related paralogues in A. thaliana (AT1G64650 and AT3G49310). A ClustalW alignment of the MOT2-family using MEGA1140 was performed to analyze sequence similarity. Alignment was visualized using BioEdit software41. The sequence of mot2.2b was excluded from this analysis due to full alignment with mot2.2a.

Molybdate transport activity of MOT2 candidates was investigated by an in vivo growth assay using transgenic Moco-yeast strains (Table S1). Growth medium pH 5.8 consisted of yeast-nitrogen-base medium (6.7 g/L; Carl Roth, Karlsruhe, Germany) was supplemented with 10x dropout solution (200 mg/L arginine, 300 mg/L isoleucine, 300 mg/L lysine, 200 mg/L methionine, 500 mg/L phenylalanine, 2000 mg/L threonine, 300 mg/L tyrosine, 1500 mg/L valine, 100 mg/L L-adenine-hemisulfate, 200 mg/L histidine, 1000 mg/L leucine, 400 mg/L tryptophan) diluted to 1x concentration and 0.2% (w/v) fructose (Duchefa Biochemie, Haarlem, Netherlands). After shaking at 200 rpm for 48 h at 30 °C, 10 mL of pre-culture inoculated with a Moco-yeast strain was added to 190 mL growth medium for main-culture and incubated analogously. Subsequently, yeast suspension was filled into 50 mL tubes and centrifuged for 15 min at 5200 × g. Supernatant was dismissed and the pellet was split into 1 mL reaction tubes, followed by centrifugation for 5 min at 5200 × g. After dismission of the supernatant, the pellet was frozen in liquid nitrogen. Galactose (Duchefa Biochemie, Haarlem, Netherlands) was added to a final concentration of 2% (w/v) to growth medium containing 250 mM sodium chlorate (NaClO3; Carl Roth, Karlsruhe, Germany) and 100 nM sodium molybdate (Na2MoO4; Sigma Aldrich, St. Louis, MI, USA) for induction of mot gene expression. For non-induction conditions the same volume of water was added instead. Growth medium was inoculated to an OD600 of 0.1 with transgenic Moco-yeast strains. A control approach contained no sodium chlorate. A 48-well MTP flower plate (m2p labs Beckman Coulter, Aachen, Germany) was loaded with 1 mL of cell suspension per well in duplicates and sealed with semi-permeable foil (F-GPR48-10, m2p labs Beckman Coulter, Aachen, Germany) to allow gas exchange. The flower plate was loaded to a BioLector® I (m2p labs Beckman Coulter, Aachen, Germany) allowing incubation of the plate shaking at 1200 rpm for 7 days at 30 °C and while simultaneous monitoring of biomass increase. Therefore, light scattering at 620 nm was detected as relative light unit (RLU)-output as biomass index. A biomass threshold of 40 RLU was selected to allow comparison of different strains and to further analyze the growth behavior. In control approaches it was shown that the influence of single growth assay components (sodium chlorate, sodium molybdate and sugar combinations) on the growth behavior of each Moco-yeast strain was neglectable.

The coding sequences (CDS) of A. thaliana genes mot2.1 (AT4G27720), mot2.2a (AT1G64650.1), mot2.2b (AT1G64650.2) and mot2.3 (AT3G49310) were amplified by Phusion polymerase (Thermo Scientific, Waltham, MA, USA) from cDNA of A. thaliana with attB site flanked primers to use the GATEWAY cloning system (Invitrogen, Waltham, MA, USA). PCR fragments were inserted into the pDONR/Zeo vector by BP reaction generating pEntry-mot2 entry vectors.

For localization studies the resulting entry vectors were recombined with pDest-GW-venus vectors using LR reaction to generate expression vectors coding for mot2-venus fusion constructs. As cytosolic marker eqFP61142 was used. To create a PM-marker, the CDS of Atpip2a (AT3G53420) from A. thaliana was amplified with attB site flanked primers and sub cloned by BP reaction into the pDONR/Zeo vector. Recombination with pDest-GW-rfp43 by LR reaction led to the expression vector pExp-Atpip2a-rfp. The Golgi marker man1 from soybean (Glycine max) was synthesized from two oligonucleotides that were annealed and amplified in a first PCR. A second PCR with attB site flanked primers allowed to use the fragment in a BP reaction to create an entry vector. A LR reaction with pDest-GW-rfp generated the expression vector pExp-GmMan-1-RFP.

Topology studies of the MOT2 family were carried out using the GATEWAY-based Split-10 + 1 GFP system22. Vectors were kindly provided by Prof. Thordal-Christensen from University of Copenhagen. LR reaction of pEntry-mot2 vectors and pDest-GW-gfp11 and pDest-gfp-GW expression vectors were generated coding for constructs with GFP11 either fused to the N- or the C-terminus of MOT2. The GFP1-10 fragment was co-expressed with either cytosolic localization (GFP1-10) or with localization in the apoplast by using the signal peptide of AtWAK2 (A. thaliana Wall Associated-Kinase 2, AT1G21270) resulting in SP-GFP1-1044.

For BiFC assays, entry vectors with CDS of mot2 and Atpip2a were recombined by LR reaction with the pDest-GW-vyne destination vector resulting in expression vectors coding for mot2-vyne and Atpip2a-vyne constructs. The C-terminal half of the cytosolic Luciferase (CLuc)24 was used as abundance control. The CDS was amplified by Phusion PCR with attB site flanked primers and used in a BP reaction to generate entry vectors. Those were used in LR reaction with pDest-GW-vyne and pDest-GW-scyce to generate pExp-Atpip2a-vyne and pExp-nsp3-scyce expression vectors. Generation of pExp-cnx1-scyce expression vectors was generated by LR reaction with the pDest-GW-scyce destination vector and the entry vector pEntry-cnx1 (AT5G20990)43.

For split-Luc analyses LR reaction using pEntry-mot2.1 and pDest-GW-cluc generated pExp-mot2.1-cluc expression vectors. Expression vectors pExp-cnx1-nluc, pExp-cnx1e-nluc, pExp-cnx1g-nluc, negative controls pExp-nsp3-nluc and abundance control pExp-scyce-nluc were generated by cloning via LR reaction the entry vectors pEntry-cnx1 (AT5G20990), pEntry-nsp3 (AT3G16390) and the BiFC-terminus pEntry-scyce into the destination vector pDest-GW-nluc45. Expression vector pExp-Atpip2a-cluc was generated by LR-reaction with pEntry-Atpip2a and pDest-GW-cluc. Primers used to generate the vectors (Table S6) of this study are listed in Table S7. Plant transformation for localization, topology, BiFC and split-Luc assay was carried out according to Minner-Meinen et al.7. Expression in N. benthamiana leaves was carried out by Agrobacterium tumefaciens mediated transformation45,46,47. Protoplast preparation and chemical transformation were carried out according to Negrutiu et al.48. A. thaliana seedlings were transformed by the FAST (fast agro-mediated seedling transformation) method49.

Germination of N. benthamiana was achieved in common potting soil at 22–25 °C with 10 h of artificial light ( ≈ 60 µE) per day under greenhouse conditions and sufficient water supply. Seedlings were transferred two weeks after germination, into 9 × 9 cm pots containing pot soil mixed with 1% NPK-fertilizer (Blaukorn® classic, Compo Expert, Münster, Germany) and 5% Perlite. Five to 12 weeks old plants were used for experiments. A. thaliana seeds were stratified at 4 °C for 48–72 h. Two weeks after germination on common pot soil, seedlings were transferred into 5 × 5 cm pots and cultivated at 22–25 °C in a walk-in phyto-chamber with 10 h of artificial light ( ≈ 60 µE) per day and 60–70% humidity.

Plants were grown in a hydroponic growth system50 modified according to Minner-Meinen et al.7. Germination and basal nutrient solution (¼ Hoagland´s solution) with a pH value of 5.6 were prepared either with 100 nM of sodium molybdate ( + Mo, molybdate availability) or by excluding sodium molybdate from the original recipe (-Mo, molybdate deprivation). A. thaliana seeds were sown on microcentrifuge tube lids with a pin-hole and placed in a germination tank. After 20 days plants were transferred to aerated tanks and harvested after a total time span of 60 days. From germination tanks seedlings were also transferred to 130 mL centrifuge tubes and grown under molybdate availability conditions for the molybdate uptake assay.

Petals and stamen of a flower of the mother plant carrying one T-DNA insertion KO were removed to avoid the self-fertilization of the ovary. Stamen harboring mature pollen from a father plant carrying a second T-DNA insertion KO was used to fertilize the prepared ovary of the mother plant. The fertilized ovary was brought to seed maturation. The harvested seeds were grown under antibiotics selection and the presence of the inherited T-DNA insertion was tested using genotyping PCR.

Endogenous promoters were defined as the region of 1998 bp (mot2.1), 1924 bp (mot2.2) and 1980 bp (mot2.3) upstream of each start codon. Regions were amplified from genomic DNA of A. thaliana by phusion PCR with attB site flanked primers. Fragments were sub-cloned using the GATEWAY cloning system (Invitrogen, Waltham, MA, USA) into pDONR/Zeo via BP reaction generating entry vectors. By recombination via LR reaction with pKGWFS751 expression vectors coding for a GFP-GUS-fusion construct expressed under the control of the endogenous mot2 promoters (mot2.1:gus, mot2.2:gus and mot2.3:gus) were generated. To generate stable A. thaliana lines, floral dip52 with Agrobacterium tumefaciens was carried out. Selection for transformants in T0 and T1 generation was carried out with kanamycin (Duchefa Biochemie, Haarlem, Netherlands). To avoid positional effects of random T-DNA integration after Agrobacterium transformation, three individually generated lines were used for further experiments. The presence of the mot2.gus constructs was tested by PCR using genomic DNA.

Histochemical and fluorimetric GUS assays are well suited to gather both, qualitative as well as quantitative information about organ-specific gene expression of the mot2-family members. Assays were carried out according Minner-Meinen et al.7. Transgenic A. thaliana mot2:gus lines were grown hydroponically under molybdate availability for histochemical staining. Plant material was incubated with GUS staining solution53 via vacuum chamber and incubated at 37 °C over night. After chlorophyll extraction with 70% (v/v) ethanol, documentation was carried out using a Keyence VHX digital microscope (Keyence, Osaka, Japan). WT plants used as control showed no background signal in the analyzed organs (Fig. S3).

Fluorimetric assay was performed with mot2.1:gus plants grown hydroponically under molybdate availability and deprivation. Plant material was separated into roots, young leaves, old leaves, shoot and flower during harvest and protein extraction was carried out in triplicates. Samples were loaded into a 96-well plate and mixed with GUS reaction solution containing methylumbelliferylglucuron (MUG; Duchefa Biochemie, Haarlem, Netherlands) that can be cleaved by GUS into the fluorescent product MU (methylumbelliferyl; excitation: 365 nm, emission: 455 nm). Fluorescence was measured using a Tristar LB941 multimode reader (Berthold Technologies, Bad Wildbad, Germany) over a time span of 40 min. GUS activity was calculated as the rate of gain in fluorescence intensity over time normalized to the amount of total protein measured via Bradford assay using Roti®Quant reagent (Carl Roth, Karlsruhe, Germany). WT plants were used as negative control and showed no fluorescence signal in the analyzed organs.

The leaf area of A. thaliana plants growing hydroponically was measured using Easy Leaf Area software54. A red square with an area of 4 cm2 was used as reference. By setting the number of green pixels into relation to the known number of red pixels the leaf area was determined in a non-invasive and rapid manner. For 60 days pictures were taken as triplicates with a Panasonic Lumix DMC-GX80 and a Panasonic H-FS 1442 A camera lens (Panasonic, Kadoma, Japan) every 2 days. Furthermore, the developmental stages of the plants were recorded55 every 2 days and overall plant survival was analyzed. After 60 days plants were harvested and fresh weight as well as root length were measured.

A. thaliana (8 weeks old) were grown in 130 mL tubes filled with molybdate containing basic nutrient solution. After two weeks the medium was harvested in 50 mL duplicates and leaf area was determined. Molybdate concentrations were measured in a modified manner according to Cardenas and Mortensen56. A sample volume of 50 mL lowered the detection limit of the assay to 10 nM molybdate. Samples were mixed thoroughly with 50 µL of sulfuric acid and 250 µL of assay reagent (2% (w/v) sodium hydroxide, 2 g/L 1,2-Dimercapto-4-methylbenzene, Thermo Scientific, Waltham, MA, USA; 16 mL/L thioglycolic acid, Supelco, Sigma Aldrich, St. Louis, MI, USA) for 1 min and shaken for 20 min. After adding 1 mL of pure isoamyl acetate, mixing for 2 min and shaking for another 20 min, the organic phase was extracted from the conical end of the tube. Extinction was measured in a solvent-resistant cuvette at 680 nm blanked against pure solvent. A calibration curve from 0 to 150 nM sodium molybdate enabled in basic nutrient solution was measured to determine molybdate concentration. The amount of absorbed molybdate was calculated and normalized with the leaf area. WT plants and mot1.1-KO plants served as positive and negative control, respectively.

The NR enzyme activity assay57 was carried out according to Minner-Meinen et al.7. Leaf material of mot2-KO lines grown hydroponically under molybdate availability and deprivation was harvested and homogenized under liquid nitrogen cooling. Homogenate was mixed with extraction buffer, mixed thoroughly and centrifuged. Assay reaction was started by mixing the extract with assay buffer and stopped after 10 min, 20 min, and 30 min by adding zinc acetate. The amount of formed nitrite was measured colorimetrical after reaction with sulfaniamid (SA; Merck, Darmstadt, Germany) and N-[Naphthyl-(1)]-ethylendiammoniumchlorid (NED; Sigma Aldrich, St. Louis, MI, USA). NR enzyme activity was calculated in nmol NO2- per mg of fresh weight and hour.

Stock solutions of reduced GSH (Duchefa, Harlem, Netherlands) and sodium molybdate (Sigma-Aldrich, St. Louis, MI, USA) were prepared in water with a concentration of 2 mM. The 2 mM GSH sample was diluted with water to a concentration of 1 mM. The spectrum of each sample was recorded by measuring the extinction of light in the UV region ranging from 190 nm to 350 nm in special UV cuvettes with a layer thickness of 1 cm using an Ultrospec 2100 pro UV/VIS spectrophotometer (Amersham Biosciences, Amersham, UK). Subsequently, the background of a sodium molybdate solution with a concentration of 1 mM was subtracted from the spectrum by blanking. The GSH and molybdate solution was mixed equimolar to a concentration of 1 mM each and the extinction spectrum was recorded.

Liquid chromatography mass spectrometry (LC-MS) measurements were performed using Q Exactive Orbitrap (high-performance benchtop quadrupole Orbitrap mass spectrometer; Thermo Fisher Scientific, Bremen, Germany) HRMS with electrospray ion source (mass range in negative mode: m/z = 100–1500) and Ultimate3000 UHPLC system (Thermo Fisher Scientific, Bremen, Germany). Samples were either injected by direct injection (flow rate was 0.6 mL·min−1) or by UHPLC. The following UHPLC conditions were used: An Accucore C18 column (2.1 × 100 mm, 2.6 μm, Thermo Fisher, Bremen, Germany) was used with gradient elution as follows: MeCN (0.1% (v/v) HCOOH)/H2O (0.1% (v/v) HCOOH) initially at 5:95, reaching 2:98 over 7 min, then maintaining 2:98 for 3 min. The flow rate was 0.2 mL·min−1 and injection volume was 3 µL. Isotopically enriched molybdenum (enrichment >98%) was purchased from Eurisotop (Saint-Aubin Cedex, France). The molybdenum oxide 98MoO3 was dissolved in sodium hydroxide solution to maintain a sodium molybdate solution. Subsequently, the prepared isotope solution was diluted with deionized water to maintain a stock solution containing 10−2 mol L−1 molybdate.

Three separate stock solutions (1 mL each) with Na2MoO4, Na298MoO4 and GSH at a concentration of 10-2 mol·L−1 in water were prepared. GSH stock solution (100 μL) was diluted with water (900 μL) prior to the MS measurement. Na2MoO4 stock solution (100 μL, 1 eq.) and GSH stock solution (100 μL, 1 eq.) were mixed and stored at room temperature (~22 °C) for 1 h. Prior to the MS measurement, the solution was diluted with water (1800 μL). The Na2MoO4 stock solution (100 μL) was diluted with water (900 μL) prior to the MS measurement. All samples were measured with HRMS by direct injection. Subsequently, solutions containing both molybdate and GSH were prepared with molar ratios of 1:1 to 1:9. Upon MS measurement, identical results were maintained, i.e. m/z = 433.9556 was detected in all samples. In addition, the pH values of the solutions were set to 3, 5, 6, 7, and 9 and measured by HRMS. In all cases, the same ion with m/z = 433.9556 was observed.

Protein-protein interaction was analyzed using bi-molecular fluorescence complementation assay43,47 according to Minner-Meinen et al.7. To allow comparable results the lower epidermis of 5–10 leaf discs from 2–3 N. benthamiana plants was analyzed with identical cLSM settings. The interaction approach included MOT2-VYNE and Cnx1-SCYCE fusion constructs expressed in one leaf half. The negative control consisted of AtPIP2A-VYNE and Cnx1-SCYCE expressed in the other leaf half. An abundance control was carried out where Cnx1-SCYCE was exchanged with the C-terminal half of cytosolic luciferase (Luc) fused to SCYCE (CLuc-SCYCE) to allow the estimation of different concentration levels of the negative control protein in correlation with the interaction approach counterpart and resulting random fluorescence signals43.

Localization, topology and BiFC studies were carried out using a confocal Laser Scanning Microscope (cLSM) LSM 510 Meta from Zeiss (Göttingen, Germany)7,46. The cLSM-510META scan head was connected to Axiovert 200 M. All objects were analyzed either with a Plan-Neofluar 10x/0.3 or a C-Apochromat 40x/1.2 water-immersion objective. Excitation was carried out using both an argon laser (488 nm line for all VENUS approaches, as well as chlorophyll auto fluorescence) or a Helium-Neon Laser (543 nm line for eqFP611). Primary beam splitting was achieved by UV/488/543/633 mirrors. Secondary beam splitters acted at 545 nm. Filter sets for the detection of fluorescence was used as followed: BP 505-530 nm for all split-GFP (Emmax: 510-515 nm) and VENUS (Emmax: 525 nm) approaches; BP 560-615 for eqFP611 (Emmax: 611 nm); LP 650 nm for chlorophyll auto fluorescence. The Lambda mode was used to examine spectral signature of all fluorophores. All images were taken using ZEISS Microscope Software ZEN 2009.

Split-Luc assay to analyze protein-protein interaction was performed by floated leaf luciferase complementation imaging (FLuCI) according to Kaufholdt et al.45. Interaction approach consisted of leaves co-expressing MOT2.1-CLuc and either Cnx1-NLuc, Cnx1E-NLuc or Cnx1G-NLuc. Negative control replaced either MOT2.1-CLuc with AtPIP2A-CLUc or Cnx1-constructs with NSP3-NLuc. Abundance control to depict signals originating from random interaction consisted of SCYCE-NLuc and replaced Cnx1-constructs. Interaction approach and negative control or abundance control were infiltrated into one leaf half each. After 2–7 days of transformation, 6 leaf discs (12 mm diameter) per leaf half from 4 leaves of 4 plants each were infiltrated with luciferin solution (10 mM MES pH 5.6, 10 mM MgCl2, 0.5% (v/v) DMSO, 0.1 mM luciferin). Luminescence was measured as RLU using a Tristar LB941 multimode reader (Berthold Technologies, Bad Wildbad, Germany) at 560 nm for 20 min. Interaction approach split-Luc factor was calculated by dividing the mean of the interaction approaches with the negative controls from the other leaf half. Abundance control split-Luc factors was calculated analogously. Interaction takes place, when the interaction approach split-Luc factor is higher than the abundance control split-Luc factor.

All experiments were performed with multiple independent samples as described in Materials and Methods and the figure legends. Experiments addressing localization, termini topology, BiFC, Split-Luc and GUS-staining were performed multiple times and had similar results to those reported here. Growth kinetics of Saccharomyces and plants are repeated at least three times. Means of independent experiments are plotted and error bars depict standard deviation. As stated in each figure/table legend, unpaired T-test was used to test for significance, two-way ANOVA analyses and Sidak post hoc tests for multiple comparison were used to analyze quantitative data. No data were excluded from results reported and all the biological replicates were used for statistical analyses.

Further information on research design is available in the Nature Portfolio Reporting Summary linked to this article.

All data supporting the findings of this study are available within the paper and its Supplementary Information. The numeric data used in the present work can be found in Supplementary Data 1 and are available from the corresponding author on reasonable request.

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We would like to thank Mattes Hintmann and the work group of Rebekka Biedendieck from the BRICS (TU Braunschweig, Germany) for help with the BioLector® and the supply with flower plates. We would like to appreciate the help of Prof. Hans Thordal-Christensen (University of Copenhagen, Denmark) for providing Split-10 + 1-GFP vectors. Arabidopsis T-DNA KO lines were kindly provided by the Nottingham Arabidopsis stock center (NASC, Nottingham, UK). Furthermore, we would like to thank Prof. Dr. Erwin Grill for help with the topic of heavy metals and glutathione. We also would like to thank the work group of Prof. Dr. Christian Hertweck for great help with mass spectrometry analyses and for sharing their facility with us. We would like to thank Nele Fiene, Moritz Friesch, Benedikt Gierling, Linda Hage, Melanie Heidecke, Jannik Heiligenstadt, Rena Hinrichs, Saskia Kell, Eike Kreitz, Jan-Hendrik Lenzen, Samuel Meckoni, Lena Meißner, Paul Meyfarth, Merve Saudhof, Fynn Schilling, Ina Schmidt, Alexa Schubert, Nico Sprotte, Luca Steinbacher, Claudia Strauch, Kaja Tünnermann, Hanna Willenbockel, Jess Arnold Siani Wouachi and Chris Zaydowicz for their help, their high commitment and great technical work in our lab. Our special thanks got to our technicians Kristin Eckhoff and Tanja Linke. This work was financially supported by the Deutsche Forschungsgemeinschaft (grant GRK2223/1) to R.H. and R.R.M.

Open Access funding enabled and organized by Projekt DEAL.

These authors contributed equally: Jan-Niklas Weber, Rieke Minner-Meinen

Institute of Plant Biology, Technische Universität Braunschweig, Humboldtstrasse 1, D-38106, Braunschweig, Germany

Jan-Niklas Weber, Rieke Minner-Meinen, Maria Behnecke, Thomas W. Hercher, Lena van den Hout, Lars Knüppel, Simon Sivov, Jutta Schulze, Ralf-R. Mendel, Robert Hänsch & David Kaufholdt

Institute of Microbiology and Braunschweig Integrated Centre of Systems Biology, Technische Universität Braunschweig, Rebenring 56, D-38106, Braunschweig, Germany

Rebekka Biedendieck

Department of Biomolecular Chemistry, Leibniz Institute for Natural Research and Infection Biology (HKI), Beutenbergstrasse 11a, Faculty of Biological Sciences, Friedrich Schiller University Jena, D-07743, Jena, Germany

Veit G. Hänsch & Christian Hertweck

Center of Molecular Ecophysiology (CMEP), College of Resources and Environment, , Southwest University, Tiansheng Road No. 2, 400715, Chongqing, Beibei District, PR China

Robert Hänsch

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J.N.W., R.M.M., R.H. and D.K. planned and designed the project. RH and RRM acquired funding. R.M.M., M.B. and J.N.W. performed in silico analysis. TWH, RRM, D.K. and J.N.W. generated yeast strains. SS, J.N.W., D.K., R.H. and R.B. performed yeast growth assays and discussed the results. R.M.M. designed and generated vectors for localization, topology and BiFC. J.S. performed protoplast isolation and transformation. R.M.M., M.B. and J.N.W. carried out localization studies. R.M.M. performed topology studies. R.M.M. and J.N.W. generated mot2:gus plant lines. Lv.d.H. carried out histochemical GUS assays. J.N.W. carried out fluorimetric GUS assays. Lv.d.H. and J.N.W. handled hydroponical growth, phenotype analysis. J.N.W. carried out molybdate uptake assays. Lv.d.H. performed NR assays. R.M.M., L.K. and D.K. carried out BiFC analyses. J.N.W. performed UV-spectra analysis of GSH-molybdate complexes. C.H. and V.H. carried out MS experiments. All authors analyzed and discussed the results. J.N.W. and D.K. were primarily involved in drafting the manuscript. J.N.W., V.H., D.K., Lv.d.H., L.K. and R.R.M. produced figures and tables. J.S., R.H. and R.R.M. critically read the manuscript and improved the text; all authors finalized it. J.N.W., D.K. and R.H. coordinated the work. All authors have read and agreed to the published version of this manuscript.

Correspondence to Robert Hänsch.

The authors declare no competing interests.

Communications Biology thanks the anonymous reviewers for their contribution to the peer review of this work. Primary Handling Editors: David Favero and Manuel Breuer. A peer review file is available.

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Weber, JN., Minner-Meinen, R., Behnecke, M. et al. Moonlighting Arabidopsis molybdate transporter 2 family and GSH-complex formation facilitate molybdenum homeostasis. Commun Biol 6, 801 (2023). https://doi.org/10.1038/s42003-023-05161-x

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Received: 04 April 2023

Accepted: 21 July 2023

Published: 02 August 2023

DOI: https://doi.org/10.1038/s42003-023-05161-x

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Moonlighting Arabidopsis molybdate transporter 2 family and GSH