Mycolic acids are unique long chain fatty acids found in the cell walls of mycobacteria including the tubercle bacillus, Mycobacterium tuberculosis. The introduction of double bonds in mycolic acids remains poorly understood, however, genes encoding two potential aerobic desaturases have been proposed to be involved in this process. Here we show that one of these genes, desA1, is essential for growth of the saprophytic Mycobacterium smegmatis. Depletion of desA1 in a M. smegmatis conditional mutant led to reduction of mycolic acid biosynthesis and loss of viability. The DesA1-depleted cells exhibited two other phenotypes: using 14[C]-labelling, we detected the accumulation of minor mycolic acid-related species that migrated faster in a silver TLC plate. Spiral Time of Flight Mass Spectroscopic analysis suggested the presence of species with sizes corresponding to what were likely monoenoic derivatives of α-mycolic acids. Additionally, conditional depletion led to the presence of free fatty acyl species of lengths ~C26-C48 in the lysing cells. Cell viability could be rescued in the conditional mutant by Mycobacterium tuberculosis desA1, highlighting the potential of desA1 as a new drug target in pathogenic mycobacteria.
Citation: Singh A, Varela C, Bhatt K, Veerapen N, Lee OYC, Wu HHT, et al. (2016) Identification of a Desaturase Involved in Mycolic Acid Biosynthesis in Mycobacterium smegmatis. PLoS ONE 11(10): e0164253. https://doi.org/10.1371/journal.pone.0164253
Editor: Laurent Kremer, Centre National de la Recherche Scientifique, FRANCE
Received: May 18, 2016; Accepted: September 7, 2016; Published: October 14, 2016
Copyright: © 2016 Singh et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: KT is an employee of Jeol Ltd. The funder provided support in the form of salaries for author KT, but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of this author is articulated in the ‘author contributions’ section. AB received grant funding from the Medical Research Council (UK). The funder provided support did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of this author is articulated in the ‘author contributions’ section.
Competing interests: This affiliation does not alter our adherence to PLOS ONE policies on sharing data and materials.
Mycobacterium tuberculosis, the bacterium that causes tuberculosis (TB), synthesises a distinct class of long-chain fatty acids termed mycolic acids. These α-alkyl, β-hydroxy fatty acids are abundant in the waxy cell wall of the tubercle bacillus and the cell walls of other mycobacteria including the leprosy bacillus Mycobacterium leprae, bovine TB-causing Mycobacterium bovis and the saprophytic Mycobacterium smegmatis. Mycolic acids are found either esterified to the terminal carbohydrate moieties of the peptidoglycan-arabinogalactan complex, or as part of the outer glycolipids, glucose monomycolate, trehalose monomycolate and trehalose dimycolate (TDM; also known as cord factor). A combination of early biochemical studies and subsequent development of mycobacterial genetics has helped unravel the pathways leading to the biosynthesis of mycolic acids [1–3]. Mycolic acids in mycobacteria consist of a longer mero-chain, and a shorter α-chain. Biosynthesis of mycolic acids is initiated by the ‘housekeeping’ fatty acid synthase, the multidomain fatty acyl synthase—I (FAS-I) that produces C16–C18 and C24–C26 fatty acids in a bimodal fashion. The latter forms the α-chain of mycolic acids. The mero-chain is synthesised by the multienzyme fatty acid synthase II (FAS-II) that extends FAS-I derived palmitoyl/stearoyl-S-CoA to yield fatty acids of chain length C60. The mero-chain then undergoes Claisen condensation with the α-chain; a reaction catalysed by a polyketide synthase, Pks13 to yield a 3-oxo, α-alkyl fatty acid [4,5], which is subsequently reduced by a mycolyl reductase to form a mycolic acid [6,7]. Core to mycolic acid structure is the generation of double bonds found in the mero-chain. M. smegmatis produces three subclasses of mycolic acids: α, α’ and epoxy mycolic acids (Fig 1); α mycolic acids contain two double bonds in the mero-chain, while α’ mycolates contain one double bond. In M. tuberculosis, formation of cis-double bonds can be a precursor for subsequent modification steps such as cyclopropanation [8–10]. Asselineau et al.  hypothesised that a C24:0 fatty acyl chain is first desaturated to a cis-Δ5-C24:1 intermediate which is then elongated by FAS-II, and subsequently desaturated to yield cis-Δ3, cis-Δ15-C34:2 merochains which are eventually elongated further and incorporated into mycolic acids. In Escherichia coli, fatty acid desaturation is brought about by the action of FabA, a dual function enzyme that catalyses both the formation of a trans-double bond in a fatty acyl-chain, and its subsequent isomerisation to the cis configuration . In the absence of FabA homologues in the genomes of mycobacteria, two alternative pathways to double bond formation have been suggested . In Streptococcus pneumoniae, the novel isomerase/dehydratase pair FabM/FabZ diverts fatty acid biosynthesis to the unsaturated mode . The M. tuberculosis homologues echA10 and echA11, have been proposed as candidates, though their predicted non-essentiality makes it unlikely that they play any role in mycolic acid desaturation . An alternative pathway involving a Δ5 desaturase has also been proposed to convert C24:0 to C24:1 prior to further elongation to yield the α-mycolate mero-chain . Such a desaturase would require molecular oxygen, and interestingly the M. tuberculosis H37Rv genome contains genes encoding three candidate aerobic desaturases: desA1, desA2 and desA3 . Of these, desA3 has been shown to be involved in the biosynthesis of oleic acid, rather than mycolic acids . Homologues of M. tuberculosis desA1, desA2 and desA3 are found in other mycobacteria incuding M. bovis, M. leprae and M. smegmatis, though desA3 is predicted to be a pseudogene in M. leprae [16,17]. Dyer et al.  attempted structural studies on DesA1 and DesA2, and while the authors were unable to obtain soluble DesA1, the solved structure of DesA2  revealed that DesA2 exists as a homodimer and is structurally related to plant fatty acid desaturases. However, differences in the variable metal binding pockets of DesA2, including a possible alternative access of ligand to the metal center, suggested a structurally distinct substrate for this mycobacterial fatty acid desaturase. This, and the extent of disorder in the inter-subunit region of the protein indicated a specialised role for DesA2. Here, we have investigated the role of desA1 in the desaturation of mycolic acid mero-chains in the fast growing M. smegmatis.
DesA1 is essential for mycobacterial viability during growth in laboratory media
The protein encoded by M. tuberculosis desA1 (Rv0824c) shares 80% identity and 90% similarity with the M. smegmatis homologue encoded by MSMEG5773 (multiple sequence alignment shown in Fig 2). To test the potential essentiality of desA1, we first attempted to generate a null mutant of desA1 in M. smegmatis by Specialized Transduction [19,20] using phΔMSMEG5773, a recombinant phage designed to replace M. smegmatis desA1 (MSMEG5773) with a hygromycin resistance cassette (hyg). Repeated transductions of M. smegmatis mc2155 with phΔMSMEG5773 failed to generate any hygromycin resistant transductants suggesting that the gene was likely to be essential for growth in laboratory media. We then proceeded to demonstrate the essentiality of desA1 using CESTET, a gene essentiality-testing tool for M. smegmatis . First, we generated a merodiploid strain containing a second, integrated copy of desA1 under the control of an acetamide-inducible promoter. Following transduction of the merodiploid strain, we were able to obtain hygromycin resistant colonies on agar plates containing acetamide. One such transductant was confirmed by Southern blot to have the native copy of desA1 replaced with hyg, and was designated ΔMsdesA1. When broth cultures of ΔMsdesA1 were transferred to fresh medium containing acetamide, they continued growing, however when cultures were transferred to medium without acetamide, a relative decrease in viable counts was observed (Fig 3) indicating that desA1 was essential for growth of M. smegmatis in laboratory media. All together, these results validated the essentiality of desA1 in M. smegmatis.
Consensus residues found in all four amino acid sequences are indicated by uppercase letters.
Loss of M. smegmatis DesA1 leads to loss of mycolic acid biosynthesis
To determine the effect of loss of DesA1 on mycolic acids we extracted 14C-labelled mycolic acids methyl esters (MAMEs) from cultures of the ΔMsdesA1 strain grown in the presence or absence of acetamide, and analysed the extracts by 2D-argentation TLC. The second TLC dimension involves separation of saturated and unsaturated species in an AgNO3-treated section of the TLC plate, as the presence of double bonds retards migration in this dimension. Cultures grown in the absence of acetamide showed a decrease in the biosynthesis of subclasses of α, α´ and epoxy mycolic acids over time (Fig 4). Additionally, we also observed a previously described cyclopropanated α-mycolate species  in both cultures (Labelled X1 in Fig 4A). Levels of X1 did not decrease following depletion of DesA1, even at the later time point. This was surprising, as cyclopropane ring formation requires double bond formation.
(A) Direction-I separated in petroleum ether:acetone (95:5, v/v); direction-II separated thrice in AgNO3 treated silica gel in petroleum ether:ethyl acetate (9:1, v/v). The cyclopropanated derivative is indicated as X1 and the faster-migrating species that co-migrated with α-MAMES in direction-I are indicated as X2. The clear ‘imprint’ appearing superimposed on the comet shaped X2 spot in the 8h –acetamide TLC is likely due to unlabelled α2 mycolates synthesised at the early stages of DesA1 depletion. (B) Bar graph showing the relative amounts of each 14C-labelled mycolate subspecies indicated as a percentages of the total amounts of 14C-labelled mycolic acids detected on the TLC plates, as determined by densitometry.
In addition to the above phenotypes, DesA1-depleted cultures also revealed the presence of faint but detectable levels of extra species of fatty acyl methyl esters that predominantly co-migrated with α-MAMEs in the first dimension, but migrated further than the α-MAMEs in the second, AgNO3-containing dimension in the TLC plate (labelled ‘X2’ in Fig 4A). This result suggested that the faster migrating spots (X2) in the 2D-TLC plates were likely fatty acyl methyl esters related to α-mycolic acids.
To further characterise mycolic acid species in the conditional mutant, we first subjected purified, non-labelled α-MAMES to high-resolution matrix-assisted laser desorption /ionization time-of-flight mass spectrometry. Unlike 14C-labelled cultures, using non-labelled cells does not offer an opportunity to study mycolates in a time dependent fashion. Instead, MAMEs extracted from non-labelled, no-acetamide cultures represent both ‘regular’ mycolates produced during the early stages of DesA1 depletion, and those produced at later stages of DesA1 depletion. The levels of these early stage ‘regular’ mycolates (which would also be present in the +acetamide cultures) would thus dominate in any subsequent analysis. Thus, the unkown, accumulating MAMEs (species X2) in the DesA1-depleted cultures would represent only a fraction of the total MAMEs extracted from non-labelled cell pellets.
The molecular masses calculated for the observed MAME species in cultures grown the presence of acetamide indicated that dienoic C77:2 and C79:2 were the major α-MAMEs in the non-depleted cultures (+acetamide; Fig 5A) though other species, including, surprisingly those with masses corresponding to monoenoic derivatives, were also present. While the DesA1 depleted cultures (-acetamide; Fig 5B) showed the presence of same species, we detected slightly higher relative peak intensities for MAMEs with sizes predicted to represent monoenoic derivatives C74:1, C76:1,C78:1 and C80:1 (Fig 5C).
A, mass spectra of α-MAMES extracted from (A) + acetamide cultures and (B)–acetamide cultures. (C) Example of predicted sizes and structures based on observed masses.
We further analysed total mycolates extracted from cultures of ΔMsdesA1 grown in the presence or absence of acetamide, using MALDI-TOF MS with a spiral trajectory [23,24]. We chose this method over conventional MALDI-TOS MS as it gives high mass resolution and accuracy, and enables the separation of adjacent peaks with a 0.036 Da mass difference. Consistent with our findings with purified α-MAMES, we observed molecular masses corresponding to both monoenoic and dienoic α-MAMES (Fig 6; S1 and S2 Figs, S1 and S2 Tables). Given the accuracy of the method in distinguishing between species differing by 0.036 Da mass differences, we were also able to account for epoxy mycolates and distinguish these from potentially monoenoic α-mycolates of similar masses. For example the epoxy mycolate species C78H152O4Na (m/z 1176.158) could be differentiated from monoenoic α-mycolate C79H156O3Na, (m/z 1176.194). However, we could not distinguish between dienoic α-mycolates and their cyclopropanated derivatives as species with the same number of carbons would have an identical mass.
While 14C-acetate labelling afforded a sensitive method for visualising newly synthesised mycolates extracted from smaller culture volumes within defined time frames, further MS and NMR analysis required non-radioactive, unlabelled samples derived from scaled up cultures. Bacterial lysis limited the amount of cell material we could collect for this analysis. Furthermore, as mentioned earlier, unlabelled cell pellets would yield mycolates synthesised both in the early and late stages of depletion and thus the observed differences between the relative levels of monenoic and dienoic mycolates were perhaps under-represented here. Given the relatively low levels of species X2 expected in non-labelled samples, we were unable to further study structural features of this species from DesA1-depleted cultures.
In summary, the 2D-argentation TLC results and subsequent MS analysis indicate that loss of DesA1 leads to changes in the relative proportions of monoenoic and dienoic derivatives of α-MAMEs following loss of DesA1 function. We cannot conclude that depletion of DesA1 led to an overall accumulation of monoenoic derivatives of α-mycolic acids. However, using Mass Spectroscopy, we were able to show changes in the relative proportions of monoenoic and dienoic derivatives following loss of DesA1 function.
In parallel, we also analysed fatty acid methyl esters (FAMES) obtained from polar and apolar lipid extracts by 2D-argentation TLC and GC-MS. Unlike MAMEs, no additional FAME species were detected in the second dimension of the TLCs (Fig 7). We further analysed FAMEs using Gas Chromatography-Mass Spectroscopy (GC-MS). The GC-MS spectra did not reveal any major differences in unsaturated species (Fig 8), indicating that the role of desA1 was associated with mycolic acids, but not other fatty acids found in M. smegmatis.
(A) Direction-I separated in petroleum ether:acetone (95:5, v/v); direction-II separated thrice in AgNO3 treated silica gel in petroleum ether:ethyl acetate (9:1, v/v). Mycolate species from apolar extracts are indicated and are also present in lesser amounts in the polar extracts. F; fatty acyl methyl esters.
Lipid analysis of the conditional mutant
In addition to studying mycolic acid profiles of the conditional ΔMsdesA1 mutant, we also compared the total lipid profile of the conditional mutant, grown in the presence and absence of acetamide, by 2D-TLC particularly using System C that allows visualisation of free fatty acid and free mycolic acid species . While cultures of ΔMsdesA1 grown in the presence of acetamide showed the patterns expected of the wild type strain (M. smegmatis mc2155), i.e. a spot each corresponding to free fatty acids (FA) and free mycolic acids (MA; Fig 9), cultures of the strain grown for 8h in the absence of acetamide showed the accumulation of a lipid species that migrated close to the free MA and FA spots (Fig 9). We then monitored the incorporation of 14C acetate by cultures of the conditional mutant at different time intervals in the presence or absence of acetamide. Analysis of 14C-labelled lipids by 2D-TLC using System C showed an accumulation of the same, unknown lipid species in cultures grown for 8h in the absence of acetamide (Fig 9). The presence of this lipid spot predominantly in the cultures growing in the absence of acetamide implied that the accumulation of the spot was directly or indirectly related to the loss of desA1 function. Furthermore, the accumulation of this lipid species was accompanied by a decrease in the levels of free mycolic acids (Fig 9) suggesting that the accumulating lipid was related to mycolic acids. As expected, we also saw a decrease in levels of TDM after conditional depletion of DesA1 (Fig 10), but no immediate reduction was seen in other apolar lipids (Fig 10). Surprisingly, 2D-TLC of polar lipid fractions revealed relatively lower levels of PIMs in the DesA1-depleted cultures, though levels of other polar lipids remained similar.
Direction-I, chloroform:methanol, 96:4 (v/v); direction-II, toluene:acetone, 80:20 (v/v). MPA, 5% ethanolic molybdophosphoric acid, followed by charring; MA, free mycolic acids; FA, free fatty acids.
System A direction I; petroleum ether:ethyl acetate 98:2 (X3), direction II; petroleum ether:acetone 98:2. System D direction I; chloroform:methanol:water 100:14:0.8, direction II; chloroform:acetone:methanol:water 50:60:2.5:3. System E direction I; chloroform:methanol:water 60:30:6, direction II; chloroform:acetic acid:methanol:water 40:25:3:6. TAG, triacylated glycerol; TMM, trehalose monoycolcate; TDM, trehalose dimycolate; PIMs, phosphatidyl inositol mannosides.
Loss of DesA1 leads to the accumulation of a series of fatty acids
The 2D-TLC patterns obtained with the ΔMsdesA1 mutant in Fig 9 suggested that the lipid species accumulating in DesA1-depleted cells could be a fatty acyl species. To further probe the chemical composition of this lipid species, apolar free fatty acyl species (free mycolic acids, free fatty acids and unknown accumulating species) from cultures grown in the presence or absence of acetamide were extracted from preparative TLC plates (separated in System C), and converted into fluorescent dimethoxycoumarin (DMC) esters of fatty acids. The DMC esters were then analysed by reverse phase HPLC analysis (Fig 11). Differences were observed in the HPLC profiles from the extracts of cultures grown in the presence or absence of acetamide. The DesA1-depleted cultures showed the presence of a series of fatty acyl species which eluted with a retention times ranging from 15 to 50 min. Comparison of elution times to fatty acid standards and those of mycolic acids suggested that these potential fatty acyl species had chain lengths ranging from approximately C26 to C48. Thus, the apolar lipid species migrating close to the free MAs in System C consisted of a mix of fatty acid species ranging from ~C26-C48.
The M. tuberculosis desA1 ortholog is functional in M. smegmatis
To test whether M. tuberculosis desA1 (Rv0824c), could function compensate for the loss of M. smegmatis desA1 in the conditional mutant, we first transformed ΔMsdesA1 with a replicating plasmid, pMV206MtdesA1, containing Rv0824c and its native promoter. We then tested the ability of this strain to survive following growth in the absence of acetamide. Three independently obtained transformants were able to survive in the absence of acetamide in the media (Fig 12). In contrast, control strains of ΔMsdesA1 containing only the plasmid vector were unable to grown on plates without acetamide (Fig 12). These results demonstrated that M. tuberculosis desA1 was able to compensate for the loss of M. smegmatis desA1 and rescue the viability of cultures of ΔMsdesA1 grown in the absence of inducer.
The aim of this study was to determine whether desA1, one of three mycobacterial genes encoding putative aerobic desaturases, played a role in the biosynthesis of mycolic acids. We demonstrated that MSMEG5773 (desA1), homologue of M. tuberculosis desA1, is an essential gene in M. smegmatis, required for growth in laboratory media. We also showed that depletion of DesA1 in a conditional mutant caused loss of mycolic acid biosynthesis and cell viability, and resulted in distinct phenotypes. The first was the accumulation of a species that co-migrated with α-MAMEs in the first dimension of 2D-TLC plates. A comparative Mass Spectroscopic analysis showed that while extracts obtained from cultures grown in the presence of absence of acetamide both contained both monoenoic and dienoic α-mycolate species (based on expected masses), depletion of DesA1 led to change in the relative proportion of the two classes, with levels of the potential monoenoic forms increasing. A conclusive role in double bond addition, and potential identification of double bond position would require a fine structural analysis of these unique species using NMR, however bacterial cell lysis in DesA1-depleted cultures limited our ability to conduct these studies, which would require milligram quantities of purified lipid.
In addition to the phenotype described above, we also observed fatty acyl species of sizes ranging from ~C28-C48 in apolar lipid extracts of cells of the conditional mutant following depletion of DesA1, with a concurrent reduction in levels of free mycolic acids. As FAS-I derived fatty acids are not known to extend beyond C26, these intermediate length fatty acyl species (~C28-C48) were thus likely to be truncated mero-mycolate species produced by aborted FAS-II elongation events resulting from a loss of DesA1-catalysed desaturation. Thus, while monenoic α-mycolate-related species were initially identified in DesA1 depleted cultures, it was likely that FAS-II mediated merochain elongation was not efficient in the absence of DesA1 and led to the observed series of truncated fatty acyl derivatives. These findings co-relate with earlier hypothesis that desaturation of mycolic acids occurs during merochain elongation [3,26].
We also observed two unexpected phenotypes in the conditional mutant. The first was that levels of a cyclopropanated derivative of α-mycolates remained unaffected by the depletion of DesA1. This was an unexpected outcome as double bond formation precedes cyclopropanation. Fatty acid cyclopropanation is known to increase cell envelope rigidity and it is likely that additional cyclopropanation occurs in residual α-mycolates in lysing cultures to counteract damage to the cell envelope following overall depletion of mycolic acid biosynthesis. The second unexpected outcome of DesA1 depletion was the reduction in the levels of PIMs (Fig 10). This was surprising, as we did not see significant alterations in levels of fatty acids that comprise PIMs in the GC-MS analysis (Fig 8). It seems likely that the observed effect of DesA1 depletion on PIMs is an indirect one.
Our studies have identified desA1 as a gene that plays a role in mycolic acid biosynthesis. Also, the conditional loss of DesA1 eventually led to cell death, and the viability of the strain could be rescued upon introduction of plasmid-borne M. tuberculosis desA1, highlighting the potential of DesA1 as a new anti-M. tuberculosis drug target.
Materials and Methods
Generation and characterisation of a M. smegmatis MSMEG5773 (desA1) conditional mutant
The genetic tool CESTET was used to generate a M. smegmatis conditional ΔMsdesA1 mutant . MSMEG5773 was PCR amplified from M. smegmatis mc2155 genomic DNA and cloned downstream of an acetamidase promoter fragment into the integrating vector pMV306 , to generate pMV306-MSMEG5773. M. smegmatis mc2155  was electroporated with pMV306-MSMEG5773 to generate a merodiploid strain mc2155::pMV306-MSMEG5773. In parallel, phΔMSMEG5773, a temperature sensitive, recombinant phage designed to replace MSMEG5773 with a hygromycin resistance marker (hyg), was generated using protocols described by Larsen et al. . Specialized Transduction using the merodiploid strain and phΔMSMEG56773 was done as previously described [21,27]. Transductants were selected at the non-permissive temperature of 37°C on selective plates containing 150 μg/ml hygromycin and 0.02% acetamide. Replacement of the native copy of MSMEG5773 by hyg was confirmed by Southern blot. One bonafide knockout, designated as ΔMsdesA1, was selected for further analysis. Conditional depletion of MSMEG5773 (DesA1) in ΔMsdesA1 to monitor mycolic acids and other lipids was done using methods described previously .
Complementation of ΔMsdesA1 with M. tuberculosis desA1
M. tuberculosis desA1 (Rv0824c) was PCR amplified along with promoter sequences 300bp upstream of the start codon, from genomic M. tuberculosis H37Rv genomic DNA and cloned into pMV206Apra, an E. coli-Mycobacterium shuttle plasmid . The plasmid was introduced into ΔMsdesA1 by electroporation . Three independent apramycin resistant transformants were tested for their ability to grow on TSB-agar plates, with or without acetamide. The ΔMsdesA1 strain was also transformed with pMV206Apra for use as a control strain.
Extraction and characterisation of mycolic acids and other lipids
Extraction of polar, apolar lipids and mycolic acid methyl esters (MAMEs) from the conditional mutant, and subsequent TLC analysis was carried out using protocols described by Dobson et al. . Dry weights of cell pellets were used as a measure to equalise loading on TLC plates. Argentation TLC was carried out as described earlier . Characterisation of the unknown lipid observed in Fig 9 was done by preparative TLC of long-chain acidic components in the apolar lipid using toluene/acetone, 8:2. To convert the acidic components into fluorescent dimethoxycoumarin (DMC) esters , a 0.4% solution of 4-bromomethyl-6,7-dimethoxycoumarin in dichloromethane, was allowed to react with the extracts overnight under phase-transfer conditions [25,32]. 0.1mg of each sample was dissolved in 50μl heptane. 20μl of each sample was placed in a new vial. A concentration of 40μg/1000μl DMC derivatised C28 was used as an internal control. 20μl of the internal control was added to vial prior to HPLC analysis. DMC-esters of saturated C20, C26 and C28 fatty acids were used as standards. DMC esters were separated on an Alltech 205250 C18 reverse phase cartridge, using a water-methanol/dichloromethane elution sequence. Purified DMC esters were eluted by 100% DCM and analysed by reverse phase high performance liquid chromatography (HPLC). HPLC analyses used a VWR Hitachi Elite Pump L-2130, LaChrom Autosampler L-2200, Column Oven L-2300, Fluorescence Detector L-2480 and Foxy Jr. Fraction Collector; data were processed by Scientific Software Inc. EZChrom Elite, version 3.1.6 software. A reverse phase (Alltech 81412 Alltima C18, 3μm 50 x 4.6mm) column was used. HPLC analysis conditions are shown below. Samples were dissolved in HPLC grade heptane (500μl) and 1 to 5μl was injected. Using a flow rate of 1ml/min, a gradient of acetonitrile/tetrahydrofuran; 100:0 to 40:60 over 70 min was used for elution. The ratio of DMC derivatised C24, 26, 28 and mycolic acids (MA) were calculated by the area under peaks from the HPLC profiles. The ratio of the net internal standard C28: MA were calculated by subtracting the background C28 from the total C28.
The GC-FID analysis of fatty acid methyl esters (FAMEs) was performed on a Shimadzu GC-2010. The FAMEs separation was achieved using a DB-225 column (30 m x 0.25 mm i.d., 0.25 μm film thickness, J&W Scientific) with a column flow of 1.26ml/min (Helium at a constant pressure of 100kPa). Injector and detector temperatures were 50°C. The Injection volume was 5ul. The column temperature was programmed initially at 50°C for 2 mins, increased at the rate of 4°C/min to 220°C, and then maintained at 220°C for a further 30.5 mins. The total program time was 75 mins.
Purification and mass analysis of MAMEs
MAMEs were detected on TLC described previously . The TLC was developed with the solvent system; benzene or n-hexane/diethylether (90:15, vol/vol), three runs. The MAMEs were purified from the TLC plate. To assign the structures, the molecular weight of each MAME was measured by MALDI Spiral-TOF neIons generated by irradiation with a 349-nm Nd:YLF laser were accelerated at 20 kV. The settings for delay time and grid voltage were optimized to stay constant at ΔM<ca. 0.03 Da at full width at half maximum (FWHM) over the range of m/z 500 to 1500. The matrix was 10 mg/mL 2,5-dihydroxybenzoic acid in tetrahydrofuran (THF). A sodium iodide solution of 1 mg/mL in THF was used as a cationization agent. MALDI mass spectra were observed in positive spiral mode by averaging 1500 individual laser shots. Three or five mass spectra for each sample were collected. The structures of MAMEs were assigned by the Rf value of TLC and the molecular weight.
S1 Fig. Spiral MALDI-TOF of MAMES isolated from ΔMsdesA1.
S2 Fig. Spiral MALDI-TOF of MAMES isolated from ΔMsdesA1.
S1 Table. Spiral MALDI-TOF of MAMES isolated from ΔMsdesA1.
- Conceptualization: KB NF AB.
- Funding acquisition: KT AB.
- Investigation: AS KB CV OL HW NV NF KT AB.
- Resources: AB.
- Supervision: AB GSB DM.
- Writing – original draft: AB NF.
- Writing – review & editing: AB NF.
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