#METABOLOMICS WORKBENCH UTM_20211118_000251 DATATRACK_ID:2934 STUDY_ID:ST001995 ANALYSIS_ID:AN003254 VERSION 1 CREATED_ON 02-08-2024 #PROJECT PR:PROJECT_TITLE Mutasynthetic production and antimicrobial characterisation of Darobactin PR:PROJECT_TITLE darobactin analogs_NMR analysis PR:PROJECT_SUMMARY There is great need for therapeutics against multi-drug resistant, Gram-negative PR:PROJECT_SUMMARY bacterial pathogens. Recently, darobactin A, a novel bicyclic heptapeptide that PR:PROJECT_SUMMARY selectively kills Gram-negative bacteria by targeting the outer-membrane protein PR:PROJECT_SUMMARY BamA, was discovered. Its efficacy was proven in animal infection models of PR:PROJECT_SUMMARY Escherichia coli, Klebsiella pneumoniae and Pseudomonas aeruginosa, thus PR:PROJECT_SUMMARY promoting darobactin A as a promising lead compound. Originally discovered from PR:PROJECT_SUMMARY members of the nematode symbiotic genus Photorhabdus, the biosynthetic gene PR:PROJECT_SUMMARY cluster (BGC) encoding for the synthesis of darobactin A can also be found in PR:PROJECT_SUMMARY other γ-proteobacterial families. Therein, the precursor peptides DarB-F, which PR:PROJECT_SUMMARY differ in their core sequence from darobactin A, were identified in silico. Even PR:PROJECT_SUMMARY though production of these analogs was not observed in the putative producer PR:PROJECT_SUMMARY strains, we were able to generate them by mutasynthetic derivatization of a PR:PROJECT_SUMMARY heterologous expression system. The generated analogs were isolated and tested PR:PROJECT_SUMMARY for their bioactivity. The most potent compound, darobactin B, was used for PR:PROJECT_SUMMARY co-crystallization with the target BamA, revealing an identical binding site to PR:PROJECT_SUMMARY darobactin A. Besides its potency, darobactin B did not exhibit cytotoxicity and PR:PROJECT_SUMMARY was slightly more active against Acinetobacter baumanii isolates than darobactin PR:PROJECT_SUMMARY A. Furthermore, we evaluated the plasma protein binding of darobactin A and B, PR:PROJECT_SUMMARY indicating their different pharmacokinetic properties. This is the first report PR:PROJECT_SUMMARY on new members of this new antibiotics class, which is likely to expand to PR:PROJECT_SUMMARY several promising therapeutic candidates PR:INSTITUTE Justus-Liebig-University Giessen PR:LABORATORY Schäberle Laboratory PR:LAST_NAME Mettal PR:FIRST_NAME Ute PR:ADDRESS Ohlebergsweg 12, 35392 Giessen, Germany PR:EMAIL Ute.Mettal@chemie.uni-giessen.de PR:PHONE +49 641 97219 142 PR:PUBLICATIONS Mutasynthetic production and antimicrobial characterisation of Ddarobactin PR:PUBLICATIONS analogs PR:DOI http://dx.doi.org/10.21228/M8XX3Q PR:CONTRIBUTORS Nils Böhringer, Robert Green, Yang Liu, Ute Mettal, Michael Marner, Seyed Majed PR:CONTRIBUTORS Modaresi, Roman P. Jakob, Zerlina G. Wuisan, Timm Maier, Akira Iinishi, PR:CONTRIBUTORS Sebastian Hiller, Kim Lewis, Till F. Schäberle #STUDY ST:STUDY_TITLE Mutasynthetic production and antimicrobial characterisation of Darobactin ST:STUDY_TITLE darobactin analogs (MS analysis) ST:STUDY_SUMMARY There is great need for therapeutics against multi-drug resistant, Gram-negative ST:STUDY_SUMMARY bacterial pathogens. Recently, darobactin A, a novel bicyclic heptapeptide that ST:STUDY_SUMMARY selectively kills Gram-negative bacteria by targeting the outer-membrane protein ST:STUDY_SUMMARY BamA, was discovered. Its efficacy was proven in animal infection models of ST:STUDY_SUMMARY Escherichia coli, Klebsiella pneumoniae and Pseudomonas aeruginosa, thus ST:STUDY_SUMMARY promoting darobactin A as a promising lead compound. Originally discovered from ST:STUDY_SUMMARY members of the nematode symbiotic genus Photorhabdus, the biosynthetic gene ST:STUDY_SUMMARY cluster (BGC) encoding for the synthesis of darobactin A can also be found in ST:STUDY_SUMMARY other γ-proteobacterial families. Therein, the precursor peptides DarB-F, which ST:STUDY_SUMMARY differ in their core sequence from darobactin A, were identified in silico. Even ST:STUDY_SUMMARY though production of these analogs was not observed in the putative producer ST:STUDY_SUMMARY strains, we were able to generate them by mutasynthetic derivatization of a ST:STUDY_SUMMARY heterologous expression system. The generated analogs were isolated and tested ST:STUDY_SUMMARY for their bioactivity. The most potent compound, darobactin B, was used for ST:STUDY_SUMMARY co-crystallization with the target BamA, revealing an identical binding site to ST:STUDY_SUMMARY darobactin A. Besides its potency, darobactin B did not exhibit cytotoxicity and ST:STUDY_SUMMARY was slightly more active against Acinetobacter baumanii isolates than darobactin ST:STUDY_SUMMARY A. Furthermore, we evaluated the plasma protein binding of darobactin A and B, ST:STUDY_SUMMARY indicating their different pharmacokinetic properties. This is the first report ST:STUDY_SUMMARY on new members of this new antibiotics class, which is likely to expand to ST:STUDY_SUMMARY several promising therapeutic candidates. ST:INSTITUTE Justus-Liebig-University Giessen ST:LABORATORY Schäberle Laboratory ST:LAST_NAME Mettal ST:FIRST_NAME Ute ST:ADDRESS Ohlebergsweg 12, Gießen, Hesse, 35392, Germany ST:EMAIL Ute.Mettal@chemie.uni-giessen.de ST:PHONE +49 641 97219 142 ST:SUBMIT_DATE 2021-11-18 #SUBJECT SU:SUBJECT_TYPE Bacteria SU:SUBJECT_SPECIES Escherichia coli SU:TAXONOMY_ID 679895 SU:GENOTYPE_STRAIN BW25113 #SUBJECT_SAMPLE_FACTORS: SUBJECT(optional)[tab]SAMPLE[tab]FACTORS(NAME:VALUE pairs separated by |)[tab]Additional sample data SUBJECT_SAMPLE_FACTORS E. coli BW25113 SA184025 Forward Primer:CCTAAGATCCCTGAGATCACGGCCTGGAACTGGACAAAAAGATTC | Reverse Primer:TTTAGAATCTTTTTGTCCAGTTCCAGGCCGTGATCTCAGGGATCT RAW_FILE_NAME=DaroB; Plasmid=pNBDaroMod SUBJECT_SAMPLE_FACTORS E. coli BW25113 SA184024 Forward Primer:CCTAAGATCCCTGAGATCACGGCCTGGAACTGGTCAAAAAGCTTC | Reverse Primer:TTTAGAAGCTTTTTGACCAGTTCCAGGCCGTGATCTCAGGGATCT RAW_FILE_NAME=DaroA; Plasmid=pNBDaroMod SUBJECT_SAMPLE_FACTORS E. coli BW25113 SA184027 Forward Primer:CCTAAGATCCCTGAGATCACGGCCTGGAACTGGTCAAGAAGCTTC | Reverse Primer:TTTAGAAGCTTCTTGACCAGTTCCAGGCCGTGATCTCAGGGATCT RAW_FILE_NAME=DaroD; Plasmid=pNBDaroMod SUBJECT_SAMPLE_FACTORS E. coli BW25113 SA184029 Forward Primer:CCTAAGATCCCTGAGATCACGGCCTGGAAGTGGTCAAAGAATCTT | Reverse Primer:TTTAAAGATTCTTTGACCACTTCCAGGCCGTGATCTCAGGGATCT RAW_FILE_NAME=DaroF; Plasmid=pNBDaroMod SUBJECT_SAMPLE_FACTORS E. coli BW25113 SA184028 Forward Primer:CCTAAGATCCCTGAGATCACGGCCTGGTCATGGTCAAAGAGCTTC | Reverse Primer:TTTAGAAGCTCTTTGACCATGACCAGGCCGTGATCTCAGGGATCT RAW_FILE_NAME=DaroE; Plasmid=pNBDaroMod SUBJECT_SAMPLE_FACTORS E. coli BW25113 SA184026 Forward Primer:CCTAAGATCCCTGAGATCACGGCCTGGTCATGGTCAAGATCATTC | Reverse Primer:TTTAGAATGATCTTGACCATGACCAGGCCGTGATCTCAGGGATCT RAW_FILE_NAME=DaroC; Plasmid=pNBDaroMod #COLLECTION CO:COLLECTION_SUMMARY E. coli strains for cloning and expression were grown in LB broth or on agar CO:COLLECTION_SUMMARY medium supplemented with appropriate antibiotics or supplements at 37° C or CO:COLLECTION_SUMMARY 30° C using standard working concentrations. Plasmid DNA was isolated using the CO:COLLECTION_SUMMARY innuPREP plasmid mini kit 2.0 (AnalytikJena, Jena, Germany) according to the CO:COLLECTION_SUMMARY manufacturer’s protocol. Genomic DNA was extracted using the innuPREP CO:COLLECTION_SUMMARY bacteriaDNA kit (AnalytikJena, Jena, Germany). PCR amplification for cloning CO:COLLECTION_SUMMARY purposes was performed using Q5 DNA polymerase (NEB Biolabs, New Brunswick, USA) CO:COLLECTION_SUMMARY according to the given instruction. Restriction digestion was performed using CO:COLLECTION_SUMMARY standard techniques and employing NEB enzymes (NEB Biolabs, New Brunswick, USA). CO:COLLECTION_SUMMARY DNA fragments were analysed on and excised from 1% or 2% TAE-agarose with CO:COLLECTION_SUMMARY GeneRuler 1kb Plus (ThermoFisher, Waltham, USA) as marker. DNA for cloning CO:COLLECTION_SUMMARY purposes was purified using the Zymoclean large fragment DNA recovery kit CO:COLLECTION_SUMMARY according to manufacturer’s instruction. DNA concentrations were determined CO:COLLECTION_SUMMARY photometrically with an Eppendorf BioSpectrometer (Eppendorf AG, Hamburg, CO:COLLECTION_SUMMARY Germany) using a 1 mm light path UV cuvette. DNA fragments to be fused by CO:COLLECTION_SUMMARY isothermal assembly were gel purified and fused using self-made isothermal CO:COLLECTION_SUMMARY assembly master mix (Nat Methods 2009, 6, 343–345) using NEB enzymes (NEB CO:COLLECTION_SUMMARY Biolabs, New Brunswick, USA). Assembled plasmids were transferred to E. coli CO:COLLECTION_SUMMARY cells using standard electroporation protocols (Nature 2019, 576, 459-464, Metab CO:COLLECTION_SUMMARY Eng 2021, 66, 123-136). Construcion of pNBDaroMod for modification of the CO:COLLECTION_SUMMARY precursor peptide was performed by linearising pNB03 (Nature 2019, 576, 459-464) CO:COLLECTION_SUMMARY by PCR using 5’ TCCCTTAACGTGAGTTTTCG-3’/ CO:COLLECTION_SUMMARY 5’-TTTTATAACCTCCTTAGAGCTCGAA-3’, amplification of truncated (3’ minus 50 CO:COLLECTION_SUMMARY nt) darA using 5’ GCTCTAAGGAGGTTATAAAAATGCATAATACCTTAAATGAAACCGTTAAA-3’/ CO:COLLECTION_SUMMARY 5’-TAGGTTTATTGCTTAATTCGTTTAGTGCTT-3’, the lacZ spacer from pCRISPOMYCES-2 CO:COLLECTION_SUMMARY (5’ CGAATTAAGCAATAAACCTAAAGTCTTCTCAGCCGCTACA-3’/ 5’ CO:COLLECTION_SUMMARY ACCTGATGGGATAAGCTTTAATGTCTTCACCGGTGGAAAG-3’) and the rest of the P. khanii CO:COLLECTION_SUMMARY DSM3369 BGC using 5’-TAAAGCTTATCCCATCAGGTTATTT-3’/ 5’ CO:COLLECTION_SUMMARY CGAAAACTCACGTTAAGGGATTACGCCGCGATGGTTTGTTTTATT-3’ and subsequent isothermal CO:COLLECTION_SUMMARY assembly of the plasmid. After transformation and selection on CO:COLLECTION_SUMMARY LBKan/Apra/IPTG/X-gal, blue colonies were picked and the correct assembly of the CO:COLLECTION_SUMMARY plasmid was corroborated by test restriction. AA modifications were designed in CO:COLLECTION_SUMMARY silico and ordered as complementary oligonucleotides with 4 nt overlap to the CO:COLLECTION_SUMMARY pNBDaroMod backbone. Oligonucleotides were annealed and assembled into CO:COLLECTION_SUMMARY pNBDaroMod using the protocol described in ACS Synth Biol 2015, 4, 723-728 and CO:COLLECTION_SUMMARY the resulting plasmids were transferred to E. coli BW25113 and selected on CO:COLLECTION_SUMMARY LBKan/Apra/IPTG/X-gal. White colonies were picked and grown in LBKan/IPTG for CO:COLLECTION_SUMMARY three days at 220 rpm and 30° C. The correct assembly of the plasmid was CO:COLLECTION_SUMMARY corroborated by UHPLC-MS profiling, i.e. detection of the expected product ion. CO:COLLECTION_SUMMARY For increased production titter, the modified BGCs were recloned into pRSF-duett CO:COLLECTION_SUMMARY using the primers 5’-GTATAAGAAGGAGATATACAATGCATAATACCTTAAATGA-3’/ 5’ CO:COLLECTION_SUMMARY TGCTCAGCGGTGGCAGCAGCTTACGCCGCGATGGTTTGTT-3’ for all constructs to match the CO:COLLECTION_SUMMARY layout of pRSF-ADC5 and produced in E. coli Bap1 (Metab Eng 2021, 66, 123-136). CO:COLLECTION_PROTOCOL_FILENAME Collection_Protocol_Mutasynthetic_production_of_darobactin_analogs.docx CO:SAMPLE_TYPE Bacterial cells #TREATMENT TR:TREATMENT_SUMMARY Purification of DaroB from the producer strain was achieved with a modified TR:TREATMENT_SUMMARY purification strategy from DaroA. Briefly, E. coli production strains were TR:TREATMENT_SUMMARY incubated for 5 days in a 2 L Erlenmeyer flask with 1 L LB medium supplemented TR:TREATMENT_SUMMARY with 50 μg/mL kanamycin at 30 °C. Cells were removed via centrifugation and TR:TREATMENT_SUMMARY the culture supernatant was mixed with XAD16N resin (Sigma-Aldrich) overnight TR:TREATMENT_SUMMARY under agitation. DaroB was subsequently eluted from the resin with a 50/50 TR:TREATMENT_SUMMARY solution of methanol and water, containing 0.1% formic acid. The eluate was then TR:TREATMENT_SUMMARY concentrated via rotary evaporator and loaded onto a cation-exchange column (SP TR:TREATMENT_SUMMARY Sepharose XL). DaroB was eluted by step gradients of 50 mM ammonium acetate pH TR:TREATMENT_SUMMARY 7, pH 8, and pH 10. Eluates were then concentrated by freeze drying, resuspended TR:TREATMENT_SUMMARY in Milli-Q water 0.1% (v/v) formic acid, and loaded onto a C18 reversed-phase TR:TREATMENT_SUMMARY high-performance liquid chromatography (RP-HPLC) column (Agilent, C18 5 µm: 250 TR:TREATMENT_SUMMARY x10mm, Restek). HPLC conditions for purification of DaroB are: solvent A, TR:TREATMENT_SUMMARY Milli-Q water and 0.1% (v/v) formic acid; solvent B, acetonitrile and 0.1% (v/v) TR:TREATMENT_SUMMARY formic acid. The initial concentration of 2% solvent B is maintained for 2 min, TR:TREATMENT_SUMMARY followed by a linear gradient to 26% B over 12 min with a flow rate of 5 mL TR:TREATMENT_SUMMARY min−1; UV detection by diode-array detector from 210 to 400 nm. Pure DaroB was TR:TREATMENT_SUMMARY then collected at 11.5 min. For purification of DaroE, fermentation broth was TR:TREATMENT_SUMMARY pelleted by centrifugation. The cell pellet was extracted using 80% acetonitrile TR:TREATMENT_SUMMARY and water by sonification. The resulting crude extract was fractionated by flash TR:TREATMENT_SUMMARY chromatography using a C18 F0120 column with the following gradient: 1) 0-28 min TR:TREATMENT_SUMMARY 5% ACN, 2) 28-37 min increased to 15% ACN, 3) 37-50 min, keeping 15% ACN, 4) TR:TREATMENT_SUMMARY 50-60 min, increased to 30% ACN, 5) 60-80 min, increased to 100% ACN and keeping TR:TREATMENT_SUMMARY 100% ACN for 15 min. By LCMS guided isolation, the DaroE-containing fraction was TR:TREATMENT_SUMMARY identified and further separated by HPLC using the following gradient: 1) 0-10 TR:TREATMENT_SUMMARY min 23% MeOH, 2)10-20 min increased to 50% MeOH, 3) 20-30 min increased to 100% TR:TREATMENT_SUMMARY MeOH, 4) 30-37 min 100% MeOH. Afterwards, the DaroE fraction was further TR:TREATMENT_SUMMARY purified by HPLC (gradient: 1) 0-5 min 25 %MeOH, 2) 5-45 min increased to 42.5% TR:TREATMENT_SUMMARY MeOH, 3) 45-52 min keeping 100% MeOH to obtain pure compound. For DaroD the same TR:TREATMENT_SUMMARY procedure via flash chromatography was followed. Then, the following HPLC TR:TREATMENT_SUMMARY gradient was applied: 1) 0-5 min 15% ACN, 2) 5-25 min increased to 25% ACN, 3) TR:TREATMENT_SUMMARY 25-30 min increased to 60% ACN, 4) 30-39 min 100% ACN. As before, a further HPLC TR:TREATMENT_SUMMARY separation followed to obtain DaroD as pure compound. TR:TREATMENT_PROTOCOL_FILENAME Treatment_Protocol_Isolation_of_compounds.docx #SAMPLEPREP SP:SAMPLEPREP_SUMMARY LCMS samples from culture supernatant, were desalted and concentrated ~ 6 times SP:SAMPLEPREP_SUMMARY using C18 stage tips before LCMS analysis. Stage tips were washed with 200 μL SP:SAMPLEPREP_SUMMARY 100 % MeOH and equilibrated using 200 μL 95:5 H2O/MeCN + 0.1 % FA and SP:SAMPLEPREP_SUMMARY centrifugation at 3000 rcf. Subsequently, 400 - 500 μL of cleared supernatant SP:SAMPLEPREP_SUMMARY were applied to the stage tips and the C18 matrix was washed with 30 μL 95:5 SP:SAMPLEPREP_SUMMARY H2O/MeCN + 0.1 % FA to remove salts. Finally, the samples were eluted using two SP:SAMPLEPREP_SUMMARY times 30 μL 20:80 H2O/MeCN + 0.1 % FA. For LCMS analysis of the pellet, cells SP:SAMPLEPREP_SUMMARY were harvested by centrifugation and the pellet was resuspended in 10 % of the SP:SAMPLEPREP_SUMMARY harvested volume 20:80 H2O/MeCN + 0.1 % FA. The resulting suspension was SP:SAMPLEPREP_SUMMARY sonicated for 10 min. Subsequently any cell debris was removed by centrifugation SP:SAMPLEPREP_SUMMARY at maximum speed for 10 min. SP:SAMPLEPREP_PROTOCOL_FILENAME Sample Preparation Protocol_Mass_Spectrometry.docx #CHROMATOGRAPHY CH:CHROMATOGRAPHY_SUMMARY High accuracy measurements were performed on a 1290 UHPLC system (Agilent, Santa CH:CHROMATOGRAPHY_SUMMARY Clara, CA, USA) equipped with DAD, ELSD and maXis II™ (Bruker, Billerica, MA, CH:CHROMATOGRAPHY_SUMMARY USA) ESI-qTOF-UHRMS with the following gradient: 0 min: 95% A; 0.30 min: 95% CH:CHROMATOGRAPHY_SUMMARY A; 18.00 min: 4.75% A; 18.10 min: 0% A; 22.50 min: 0% A; 22.60 min: 95% CH:CHROMATOGRAPHY_SUMMARY A; 25.00 min: 95% A (A: H2O, 0.1% formic acid; B: acetonitrile, 0.1% formic CH:CHROMATOGRAPHY_SUMMARY acid; flow: 600 μL/min). The employed column was an Acquity UPLC BEH C18 CH:CHROMATOGRAPHY_SUMMARY 1.7 μm (2.1 × 100 mm) column with an Acquity UPLC BEH C18 1.7 μm CH:CHROMATOGRAPHY_SUMMARY VanGuard Pre-Column (2.1 × 5 mm). The column oven temperature was CH:CHROMATOGRAPHY_SUMMARY maintained at 45°C. The injection volume was either 1 or 2 µL. CH:METHODS_FILENAME Chromatography_Protocol.docx CH:INSTRUMENT_NAME Agilent 1290 Infinity CH:COLUMN_NAME Waters Acquity BEH C18 (100 x 2mm,1.7um) CH:COLUMN_TEMPERATURE 45 °C CH:FLOW_RATE 600 μL/min CH:SOLVENT_A 100% water; 0.1% formic acid CH:SOLVENT_B 100% methanol; 0.1% formic acid CH:CHROMATOGRAPHY_TYPE Reversed phase #ANALYSIS AN:ANALYSIS_TYPE MS AN:ANALYSIS_PROTOCOL_FILE Mass_Spectrometry_Protocol.docx #MS MS:INSTRUMENT_NAME Bruker maXis II MS:INSTRUMENT_TYPE QTOF MS:MS_TYPE ESI MS:MS_COMMENTS For standard measurements on the Agilent Infinity 1290 + Bruker maXis II system MS:MS_COMMENTS MS data was acquired over a range from 50 to 2000 m/z in positive mode. Auto MS:MS_COMMENTS MS/MS fragmentation was achieved with rising collision energy (for single MS:MS_COMMENTS charged ions: 35–70 eV over a gradient from 500 to 2000 m/z; for double MS:MS_COMMENTS charged ions: 25–50 eV over a gradient from 500 to 2000 m/z). Calibration of MS:MS_COMMENTS mass spectra was achieved using sodium formate in H2O/ iPrOH (1:1) as internal MS:MS_COMMENTS standard. Mass spectra were analysed using Bruker Data Analysis 4.2 software MS:MS_COMMENTS (Bruker Daltonics, Bremen, Germany). Masses of the expected compounds were MS:MS_COMMENTS determined using ChemDraw Professional 16.0.1.4 (PerkinElmer, Waltham, USA) and MS:MS_COMMENTS recorded chromatograms were extracted for the respective m/z. Ions with fitting MS:MS_COMMENTS m/z (Δ<10 ppm) and plausible retention time were fragmented and fragments MS:MS_COMMENTS were matched to in silico identified plausible decay products. MS:ION_MODE POSITIVE MS:CAPILLARY_VOLTAGE 4500 #MS_METABOLITE_DATA MS_METABOLITE_DATA:UNITS N/A (structure elucidation) MS_METABOLITE_DATA_START Samples SA184024 SA184027 SA184029 SA184028 Factors Forward Primer:CCTAAGATCCCTGAGATCACGGCCTGGAACTGGTCAAAAAGCTTC | Reverse Primer:TTTAGAAGCTTTTTGACCAGTTCCAGGCCGTGATCTCAGGGATCT Forward Primer:CCTAAGATCCCTGAGATCACGGCCTGGAACTGGTCAAGAAGCTTC | Reverse Primer:TTTAGAAGCTTCTTGACCAGTTCCAGGCCGTGATCTCAGGGATCT Forward Primer:CCTAAGATCCCTGAGATCACGGCCTGGAAGTGGTCAAAGAATCTT | Reverse Primer:TTTAAAGATTCTTTGACCACTTCCAGGCCGTGATCTCAGGGATCT Forward Primer:CCTAAGATCCCTGAGATCACGGCCTGGTCATGGTCAAAGAGCTTC | Reverse Primer:TTTAGAAGCTCTTTGACCATGACCAGGCCGTGATCTCAGGGATCT Darobactin A Darobactin D Darobactin E Darobactin F MS_METABOLITE_DATA_END #METABOLITES METABOLITES_START metabolite_name pubchem_id inchi_key kegg_id other_id other_id_type ri ri_type moverz_quant Darobactin A 3.7 483.7089 Darobactin D 3.7 497.7119 Darobactin E 3.5 470.2034 Darobactin F 2.7 487.2482 METABOLITES_END #END