alexa Influence of Cytosolic Malic Enzyme in Oleaginous Yeast Rhodotorula mucilaginosa IIPL32 for Lipid Biosynthesis | Open Access Journals
ISSN: 1948-593X
Journal of Bioanalysis & Biomedicine
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Influence of Cytosolic Malic Enzyme in Oleaginous Yeast Rhodotorula mucilaginosa IIPL32 for Lipid Biosynthesis

Sheetal Bandhu1,2, Tripti Sharma1, Deepti Agrawal1,2, Debashish Ghosh1,2, Dilip K Adhikari1,2 and Diptarka Dasgupta1,2*

1Biotechnology Conversion Area, Biofuels Division, CSIR-Indian Institute of Petroleum, Mohkampur, Dehradun, Uttarakhand, India

2Academy of Scientific and Innovative Research (AcSIR), Chennai, Tamil Nadu 600113, India

*Corresponding Author:
Diptarka Dasgupta
Biotechnology Conversion Area
Biofuels Division
CSIR-Indian Institute of Petroleum
Mohkampur, Dehradun, Uttarakhand, India
Tel: +91 135 2525763
E-mail: [email protected]

Received Date: March 20, 2017; Accepted Date: March 31, 2017; Published Date: April 11, 2017

Citation: Bandhu S, Sharma T, Agrawal D, Ghosh D, Adhikari DK, et al. (2017) Influence of Cytosolic Malic Enzyme in Oleaginous Yeast Rhodotorula mucilaginosa IIPL32 for Lipid Biosynthesis. J Bioanal Biomed 9:100-106. doi: 10.4172/1948-593X.1000161

Copyright: © 2017 Bandhu S, 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.

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Abstract

A cytosolic NADP+ dependent malic enzyme has been purified and characterized from an oleaginous yeast Rhodotorula mucilaginosa IIPL32 to investigate its role in lipid biosynthesis. The enzyme has selective and high affinity for NADP and L-malate. Sesamol, a nonoil component of sesame seed oil, has been used during nitrogen depleted condition to evaluate inhibition of malic enzyme and lipid production. Sesamol did not inhibit purified malic enzyme. Sesamol was converted into catechol like metabolite to impart enzyme inhibition and thus lipid production by decreased supply of NADPH+.

Keywords

Malic enzyme; Oleaginous yeast; Purification; Lipid; Sesamol

Introduction

Microbial single cell oil has been visualized as an alternative to plant based natural fatty oils as feedstocks for biofuels or oleochemicals, owing to its short generation time, low space requirement and product uniformity independent of climate and geography. Oleaginous yeasts are advantageous over oil bearing microalgae, as the former could be harvested for lipid synthesis using cheap carbon sources under controlled conditions with higher productivity, against the latter, which depends on atmospheric CO2 as carbon source with less productivity [1]. Yeast lipid is generally quantified in two ways; first, percentage lipid with respect to dry cell mass and second, amount of lipid generated by conversion of sugar. Latter represents more realistic real time features, based on yield and economics. Theoretically, sugar to lipid conversion is maximum 33% however; practically ~20-22% conversion has been achieved in oleaginous yeasts [2]. Lipid biosynthesis in yeast occurs in cytosol under nitrogen limiting condition, with acetyl CoA as the initiating unit and NADPH+ as reducing equivalent [3]. Requisite NADPH+ is generated by the pentose phosphate pathway (PPP) and NADP+ dependent cytosolic Malic Enzyme (ME). Cytosolic ME activity has been reported to alter proportionally during lipid accumulation phase suggesting its crucial role in fatty acid biosynthesis [4]. NADPH+ supply in absence of cytosolic ME in oleaginous yeasts like Yarrowia lipolytica and Lipomyces starkeyi is met by PPP, however, in M. alpina supply of reluctant is met by both [2,5,6]. This is further supported from the stoichiometry of fatty acid synthesis as the lipid yield would be less, in absence of cytosolic ME when PPP was the sole NADPH+ provider. Rhodotorula sp. are reported as promising oleaginous yeast, to generate intracellular lipid body from low cost renewable feedstock derived pentose and hexose sugars. In this paper, we have evaluated the presence and role of cytosolic ME in Rhodotorula mucilagenosa IIPL32, as a supplier of NADPH for lipid biosynthesis. The enzyme was purified and characterized to confirm its affinity towards L-malate and NADP+. Effects of selective inhibitors were also correlated to enzyme activity and lipid production.

Experimental Methodologies

Materials and microorganism

Lignocellulosic hydrolysate (xylose rich) was generated in Biotechnology Conversion Area (CSIR-IIP) as per our earlier report [7]. Standards for lower carbon chain fatty acids (C6:0 to C14:0) palmitic acid (C16:0), palmitoleic acid (C16:1), stearic acid (C18:0), oleic acid (C18:1), linoleic acid (C18:2), linolenic acid (C18:3) and Sesamol, catechol and other inhibitors were procured from Sigma and were of analytical grade. All other chemicals and reagents were bought locally and were either of analytical or commercial grades.

Rhodotorula mucilaginosa IIPL32 (RMIIPL32), isolated from soil of oil dumping shed in CSIR-Indian Institute of Petroleum, Dehradun and optimally grown at 32°C, was used as oleaginous yeast for this experimental study. Cell biomass generation, lipid accumulation and ME activity were conducted in a designed medium (composition in g/L; xylose rich lignocellulosic biomass hydrolysate, adjusted to 20.0; (NH4)2SO4, 1.98; KH2PO4, 1.26; Na2HPO4, 0.748; MgSO4, 0.7; CaCl2, 0.05; MnSO4, 0.005; H3BO3, 0.005; CoNO3, 0.005; NH4MoO4, 0.005; yeast extract 1.0; pH 4.5-5.0). Taxonomic characterization of the yeast was done based on partial nucleotide sequence of 18S rDNA gene, amplified using forward (5’ ACCCGCTGAACTTAAGC3’) and reverse (5’CCGTGTTTCAAGACGGG3’) primers with genomic DNA as template. Amplified DNA was sequenced via paired end (PE) DNA sequencing method and aligned (BLASTN) with submitted sequences available in NCBI database to classify the isolate as R. mucilaginosa (Gen Bank accession number KF313359; MTCC 25056) (Figure 1).

bioanalysis-biomedicine-distance-matrix

Figure 1: Phylogenetic dendrogram, indicating the position and distance matrix based comparison of the oleaginous yeast Rhodotorula mucilaginosa IIPL32 (Gen Bank accession number KF313359). The numbers in bracket indicate accession number of the organisms.

Quantitative estimation of lipid and ME

Cell biomass generation, lipid accumulation and ME production were accomplished in 15 L fermenter (BioSac, India; working volume of 12 L equipped with automated control and SCADA) at 32°C and pH 4.5. An initial growth phase of 24 h (consumption of 90% pentose sugar) was followed by maturation phase where the carbon-to-nitrogen (C/N) ratio in the broth was increased by pumping of concentrated pentose sugar solution. During maturation phase, cell biomass was harvested after 80% consumption of sugar to recover lipid and ME from R. mucilagenosa (henceforth designated as RMME).

Lipid rich cells were collected by gravity settling and oven dried (60°C). Lipid was gravimetrically extracted with chloroform (CHCl3) and methanol (CH3OH) in a 2:1 ratio as solvent system. Fatty acid compositions were profiled in multidimensional GC (Agilent, USA) after transesterification with BF3 as described by Patel et al. with certain modifications [8].

To determine RMME activity, cell pellet was washed with deionized water and resuspended in lysis buffer (50 mM triethanolamine-HCl, pH 7.4, 1 mM EDTA, 20% w/v glycerol, 1 mM dithiothreitol) for disruption in high pressure homogenizer (Panda Plus 2000, Gea) with continuous recycling for 30 min. RMME activities were estimated as per Qiguo et al. with minor modifications using a U2900 UV-Vis spectrophotometer (Hitachi, Japan) for 5 min at 340 nm after 1 min delay time to nullify endogenous reduction of 0.3 mM NADP [9]. NADPH (extinction coefficient 6.22 × 103 L/M/cm) generation was measured as variance in absorbance for a defined time span. Reaction mix contained 66.6 mM triethanolamine HCl buffer, 5 mM MnCl2, 3.33 mM malate, and 0.33 mM NADP apart from enzyme solution. Each activity determination was made in triplicate sets with standard deviations not exceeding 5%. Enzyme activity was also determined by replacing NADP with NAD to confirm its cytosolic presence. One unit of ME activity was defined as the amount of enzyme required to catalyze the formation of 1μmol of NADPH+ per min under specified conditions. Total protein was determined by the method of Bradford with bovine serum albumin as standard [10].

Effect of sesamol on of malic enzyme and lipid production

Sesamol, a nonoil component of sesame seed oil was reported to inhibit ME activity and affect lipid production. After cell biomass generation in fermenter, sesamol (0 mM, 5 mM and 10 mM) and catechol (10 mM) were separately added along with concentrated sugar solution (biomass prehydrolysate to enhance C/N ratio for lipid accumulation). Batches were terminated after 24 h and in between intracellular lipid contents and ME activity were measured in every 6 h interval as described.

Purification of malic enzyme

RMME was purified to homogeneity in two steps. Entire purification procedure was carried out at 4°C unless indicated otherwise. Crude enzyme extract was loaded in a MacroSep High S (Bio-Rad, USA) cation exchange column (20 × 1.85 cm) pre-equilibrated with 10 mM Tris-HCl buffer containing 2 mM β-mercaptoethanol and 10% glycerol (pH 7.4). The column was eluted (1 ml/min) with same buffer until absorbance of effluent (λ280) became zero. Each fraction of 2 mL was collected and those with high specific activity were pooled and lyophilized. Lyophilized powder was re-dissolved in minimum volume of same buffer solution and was passed through pre-equilibrated adenosine 2’,5’-bisphosphate agarose (Sigma–Aldrich, USA) column (5.0 × 0.70 cm). Column was then washed until λ280 nm of effluent reached zero. Bound proteins were eluted by NADP gradient (0–100 μM) in same buffer. Fractions were collected at a flow rate of 20 mL/h and active fractions were pooled [11]. Purified protein migrated as single band in gel electrophoresis and was activity stained against 5% acetic acid after 2 h immersion into a solution of 55 mM triethanolamine-HCl buffer (pH 7.4), 0.47 mM NADP, 17.2 mML-malate, 2.75 mM MnC12, 0.55 mg/ ml nitrobluetetrazolium and 0.097 mg/ml phenazinemethosulfate [11].

Enzyme characterization

RMME was characterized to identify its kinetics parameters, role of divalent cations and effect of inhibitors to correlate its role in lipid accumulation. In vitro characterizations were performed under optimum pH and temperature.

Influence of pH on RMME activity was determined within pH ranges of 4.0–9.0 by adjusting reaction mixture with 66.6 mM of various buffer solutions, viz. N-methyl piperazine (pH 4.0-5.5), piperazine (pH 6.0-6.5), and triethanolamine-HCl (pH 7.0–9.0). Enzyme activity was quantified as mentioned earlier. Thermostability of RMME was investigated by pre-incubating enzyme solutions at 15–55°C for 90 min. After 15 min interval, residual activities were quantified as per protocol mentioned and compared with non-pre-incubated sample. Each enzyme activity was quantified in triplicates and further characterizations were performed under optimized pH and temperature.

Initial reaction rate for NADP reduction was calculated by estimating RMME activity at different malate (0.25 to 5.0 mM) and NADP (0.025 to 0.5 mM) concentrations. Michaelis Menten constant (Km) and rate of reaction (Vmax) were determined by Lineweaver and Burk plot [12]. Effect of various metal ions was investigated by quantifying RMME activity with 5 mM metal salts of Mn2+, Ca2+, Fe3+, Fe2+, Co2+, Cu2+, Mg2+, Zn2+, and Ni2+. Enzyme activity quantified in absence of metal salt was considered as 100% and residual activity was determined accordingly. To study the effect of inhibitors, RMME was incubated for 15 min in 66.6 mM triethanolamine-HCl buffer (pH 7.4) with inhibitors (EDTA, idoacetamide, tosylphenylalanyl chloromethyl ketone (TPCK), 4-chloromercurobenzoic acid, Phenyl Methane Sulfonyl Fluoride (PMSF), phenylglyoxal hydrate and pepstatin A, sesamol and catechol at a final concentration of 1 mM. Residual enzyme activity was determined in same way as stated before and activity without any inhibitor was considered 100%.

Analytical techniques

Residual xylose in biomass hydrolysate during yeast growth and lipid maturation were quantitatively analyzed with HPLC (UFLC, Shimadzu, Japan) with PL Hiplex-H acid 8 μm column (100 × 7.7 mm diameter, by PL Polymer laboratory, UK) using a Refractive Index (RI) detector. Column was eluted with a mobile phase of 1 mM sulfuric acid at a flow rate of 0.7 ml/min and oven temperature was maintained at 70°C.

Total nitrogen was analysed in TN 3000 Total Nitrogen Analyzer (Thermo Fisher, USA) as per ASTM D 4629.

Dry cell mass was determined with known quantity of cellular broth (1 ml) by hot air drying of cell pellets in microfuges. Average of triplicate data was considered for dry cell mass determination.

Qualitative multi-dimensional gas chromatograph analyses (GC × GC) were performed for transesterified lipid with Agilent 7890B GC (California, United States) fitted with a thermal modulator assembly, FID and three different capillary columns (PAC Analytical, Canada) (1st dimension non-polar, 30 m × 250 μm × 0.25 μm; 2nd dimension mid-polar, 10 m × 320 μm × 0.25 μm and bleed column, 4.7 m × 100 μm × 0.25 μm) connected serially with thermal modulator. Oven temperature was programmed from 40°C (7 min holdup) to 270°C (20 min holdup) with different ramping rates. Helium was used as a carrier gas under constant flow (0.8 ml/min) mode. All samples were analyzed in splitless mode (100:1) at an injection temperature of 250°C. 0.4 μL injection of samples was performed with a 10 μL micro syringe.

Results and Discussion

Cytosolic ME convert L-malate into pyruvate with reduction of NADP+ into NADPH+, and generated NADPH+ is used in lypogenesis along with PPP’s NADPH+ pool. In the following sections, we have discussed the confirmation of NADP+ dependent cytosolic malic enzyme, present in RMIIPL32 and correlated its role in lipid production.

Effect of sesamol for production of lipid and malic enzyme

RMIIPL32 produced 8.3 g/L yeast biomass during growth, with Yx/S=0.415 and an overall lipid content of 0.30 g/L in 24 h. Increase in C/N ratio after growth phase, resulted in total non-polar lipid accumulation of 3 g/L within next 28 h with ~80% consumption of sugar. Lipid accumulation improved with increase in RMME activity over the entire fermentation cycle. Lipid yield during maturation phase was 0.21 g/g of dry cell biomass (Figure 2) corresponding to maximum RMME activity of 0.012 U.mg-1. Fatty acid profiles depicted presence of higher monounsaturated fatty acids (MUFA) namely palmitoleate and oleate along with highest content of Saturated Fatty Acids (SFA) namely palmitate and stearate and absence of Poly Unsaturated Fatty Acids (PUFA). Such composition would lead to a fuel with better cetane number, high Cold Filter Plugging Point (CFPP) and oxidative stability (Table 1) [13]. Sesamol affected cytosolic ME activity and inhibit cell growth and lipid biosynthesis in RMIIPL32. Sesamol was added at the onset of lipid maturation phase, along with concentrated sugar solution to determine its effect in RMME activity and lipid yield under nitrogen depleted condition. Overall lipid content was reduced by 64.32%, with inclusion of the inhibitor even at low concentration (5 mM) with ~50% attenuation in RMME activity. Sesamol was proposed to produce catechol like compound by undergoing the removal of its methylene carbon [14]. This imparted its inhibitory effect to ME and thereby decreased fatty acid accumulation through limited NADPH supply. Apart from drastic change in lipid quantity, fatty acid profiles were also affected. Absence of MUFA downgraded the fuel properties. Further increase in sesamol concentration completely abolished RMME activity with minimum lipid production (1 to 2 % w/w cell lipid) that ensured cell survival. Increase in yeast biomass during the maturation phase was primarily attributed to cell biomass generation. Similar profile was depicted in case of catechol based lipid maturation, where negligible fatty acids were reflected in GC × GC. Inhibitions in lipid production were reported in R. toruloides, C. utilis and S. cerevisae, when sesamol was used to determine ME activity as well as lipid production in bioreactor [15].

bioanalysis-biomedicine-cell-biomass

Figure 2: Time course profile of xylose consumption, elemental nitrogen deletion, cell biomass generation, lipid production and RMME activity in fermenter. RMME activity and lipid production were only investigated during lipid maturation phase.

Inhibitor Concentration Cell biomass RMME Lipid yield Fatty acid profile
mM Dg U.mg-1 protein Dg? ≤ C6 to ≥ C14 C16 C16:1 C18 C18:1 C18:2 C18:3
Sesamol 0 71.83 0.026 32.43 + ++ + ++ ++ + -
5 55.68 0.011 11.57 + + - + - - -
10 8.36 0 1.53 + - - - - - -
Catechol 10 6.82 0 1.38 + - - - - - -

Table 1: Effects of sesamol and catechol for production of cell biomass, lipid and activity of RMME during lipid maturation phase; Δg and Δg? indicate difference in cell biomass as well as hexane extracted lipid in grams respectively, between growth phase and maturation phase (up to 80% consumption of sugar during maturation in 12 L fermenter batch); during growth phase 99.6 g cell biomass with 36.3 g non polar lipids were generated; + indicates presence of fatty acids with corresponding carbon numbers, ++ indicates presence of corresponding fatty acids in higher quantity and–indicates absence of corresponding fatty acids as per GC × GC.

Characterization of RMME

RMME was purified and characterized in detail. Approximately 23.25-fold purification of crude enzyme was achieved with ~13.48% recovery and specific activity of 0.279 U/mg proteins (Table 2). Purified enzyme migrated as a single band in gel-electrophoresis (Mr~200 kD), suggesting its homogeneity (Figure 3). Evans and Ratledge reported ME from Rhodosporidium toruloides CBS14 with a molecular size of 205 kDa [16]. The molecular weight is in accordance with literature reported purified ME from other microbial origins [17,18]. Song et al. identified 4 isoforms of ME and reported possible role of isoforms III and IV (~90 kD each) in lipid biosynthesis [19].

Purification steps Total activity (U) Total protein (mg) Specific activity (U.mg-1) Purification fold Recovery (%)
Crude 11.8 999 0.012 1.00 100.000
Cation Exchange Chromatography 6.3 63 0.100 8.33 53.39
Affinity Chromatography 1.59 5.7 0.279 23.25 13.48

Table 2: Summary of results of the purification of the RMME from Rhodotorula mucilagenosa IIPL32.

bioanalysis-biomedicine-electrophoresis

Figure 3: Gel electrophoresis and activity staining of purified RMME (Lane L: Ladder; Lane C: Crude RMME; Lane X: RMME after cation exchange chromatography; Lane P: Purified RMME; Lane Z: Zymogram).

RMME showed optimal activity at pH 7.0 (Figure 4a) and 15°C temperature. The pH profile is similar to the other reported MEs from human breast cancer cell (7.2), and little lower than that of M. alpine (7.5) [17,20]. Between pH 6.0 and 8.0, RMME retained over 50% of its activity and beyond that a sharp loss in activity was noticed. This might be attributed to changes in protonation state of its active site residues which catalysed the oxidative decarboxylation. Activity of RMME was reduced with lowering of pH, whereas maximum enzyme activity related to lipid production in fermenter was observed at pH 4.5. Temperature optimum for RMIIPL32 was found to be 32°C for maximum cell biomass generation as well as lipid maturation (data not given). However, in vitro, RMME was found to be thermolabile. It was most active at 15°C upto 90 min, and at 25°C it remained stable upto 45 min. Elevation in temperature beyond 25°C resulted in marked performance decrease, with no oxidative activity at 55°C (Figure 4b). Temperature profiling under different incubation periods demonstrated a typical activity pattern of RMME. Protein half-life of 45, 15 and 5 min were observed with increased incubation temperature of 35, 45 and 55°C respectively.

bioanalysis-biomedicine-temperature

Figure 4: a) Effect of pH on RMME activity, b) Effect of temperature on RMME stability.

Cofactor specificity and Kinetic determinations

RMME activity was observed with only NADP+ as cofactor. A negligible change in absorbance (with L-malate as substrate) was detected when NADP+ was replaced by NAD+ (Figure 5) and confirmed the preference of NADP+ over NAD+ for oxidatively decarboxylation of L-malate. Km and Vmax values were determined to be 0.500 mM and 0.503 (IU/mg) respectively for L-malate (Figure 6) and 0.37 mM and 1.13 (IU/mg) respectively for NADP (Figure 6). Km for L-malate was observed to be in between that of M. circinelloides (0.4 mM) and R. toruloides (0.7 mM) [16]. RMME Km for NADP was comparable to that of Mortierella alpina (0.38 mM) and higher than that of Mucor circinelloides (0.32 mM) [18,19]. Low Km value of RMME for both L-malate (0.5 mM) and NADP (0.37 mM) confirmed high affinity for the substrate as well as coenzyme, leading to faster NADPH+ generation for lipid biosynthesis.

bioanalysis-biomedicine-Cofactor-specificity

Figure 5: Cofactor specificity for RMME.

bioanalysis-biomedicine-Lineweaver-Burk

Figure 6: Km determination for RMME varying (a, a1) L-malate (at NADP conc. 1.66 mM) and (b, b1) NADP (at L-malate conc. 4.16 mM) using Michaelis-Menten and Lineweaver-Burk plots respectively.

Effects of metal ions

RMME activity was studied on different metal ions as shown in Table 3. Loss of over 50% activity was depicted with Zn2+, Cu2+, Fe3+ and Ni2+, whereas almost complete activity were retained with Mg2+ and Co2+. Mn2+ and Ca2+ enhanced enzyme activity which acted by stabilizing its quaternary structural integrity during catalysis [21]. Pry and Hsu have reported the order of events for pigeon liver ME wherein Mn2+ binds first, followed by NADP and malate [22]. Metal ion presumably act by polarizing the carboxyl group of the oxaloacetate intermediates during decarboxylation, in agreement with the accepted theory of metal assisted decarboxylation of β-keto carboxylic acids [23]. Zn2+ strongly suppressed~65% RMME activity similar to the inhibition reported in Escherichia coli [24]. Divalent Cu2+ has been known to inhibit ME activity and RMME activity was decreased by more than 50%. Cu2+ ions have been purposely, used in Aspergillus niger, where with addition of Cu2+ at the early stage of fermentation to abolish ME activity, was an effective strategy to decrease total lipid [25].

Metal ions Specific activity Relative activity
U.mg-1 protein %
Control 0.202 100.00
Mn2+ 0.279 138.13
Mg2+ 0.193 95.68
Ca2+ 0.235 116.55
Co2+ 0.192 94.96
Fe2+ 0.129 64.03
Zn2+ 0.070 34.53
Cu2+ 0.087 43.17
Fe3+ 0.044 21.58
Ni3+ 0.067 33.09

Table 3: Effects of metal ions on the activity of RMME from Rhodotorula mucilagenosa IIPL32.

Effects of inhibitors

Decrease in RMME activity in presence of various inhibitors suggested the possible presence of these amino acids in enzyme’s active site. Inhibitors effects were investigated on activity of RMME to ascertain the string of functional amino acid residues in the catalytic site. Maximum inhibition was obtained with 4-chloromercurobenzoic acid (22.06%) which was a circumstantial evidence for the presence of cysteine in the enzyme’s active site. The result was in accordance with for duck liver ME, where cysteine played important role in binding of L-malate and divalent metal ions. Pepstatin A (64.15%), PMSF (66.98%), iodoacetamide (71.29%), EDTA (89.11%), TPCK (85.85%) had inhibitory effect for RMME activity, while phenylglyoxal hydrate did not inhibit RMME [26]. PMSF acts as covalent modifier of serine in proteases. It was concluded that serine might be present in the RMME active site and could play a key role in binding of either NADP or the L-malate moiety. TPCK and Pepstatin A were selective for histidine and arginine/aspartate respectively [27,28]. Importance of thiol groups for RMME activity was confirmed by the inhibitory effect of idoacetamide. In vitro RMME was not inhibited by sesamol; rather catechol resulted in ~90% activity inhibition. Sesamol might be assimilated by RMIIPL32 to yield catechol or similar compounds, which might impart activity inhibition by irreversible binding with RMME [14]. This also supported the inhibitory role of sesamol for RMME activity and lipid production (Table 4).

Inhibitors Specific activity Relative activity
U.mg-1 protein %
Control 0.279 100
Phenyl glyoxal hydrate 0.279 100
EDTA 0.249 89.11
Iodoacetamide 0.199 71.29
TPCK 0.240 85.85
PMSF 0.187 66.98
Pepstatin A 0.179 64.15
4-chloromercurobenzoicacid 0.062 22.06
Sesamol 0.268 96.05
Catechol 0.044 15.81

Table 4: Effects of inhibitors on the activity of RMME from Rhodotorula mucilagenosa IIPL32.

Conclusion

Rhodotorula sp., being non model oleaginous yeast, lack of available genetic information prompted us to investigate the presence and role of cytosolic ME for lipid biosynthesis. Purification and characterization of RMME confirmed its cofactor specificity and high affinity for NADP+. Correspondingly, RMME activity inhibition by sesamol and catechol established its role in lipid biosynthesis by supplying NADPH+ in RMIIPL32. By this study, we conclude that supply of reductants for lipid biosynthesis could be sufficed by RMME, apart from pentose phosphate pathway in RMIIPL32. Based on fatty acid profile, RMIIPL32 lipid can be transesterified to generate high quality biodiesel.

Authors’ Contributions

SB, TS, DA, DG and DDG designed overall research plan, study oversight and conducted hands-on experiments with data collection along with drafting of the manuscript; SB and DG had primary responsibility of data representation and final shaping of the manuscript; SB carried Experimental work with TS and DA. DDG and DKA supervised overall work and participated in result interpretation with SB, TS and DG; DDG is also the corresponding author. All authors read and approved the final manuscript.

Acknowledgments

Authors thankfully acknowledge Dr. Anjan Ray, Director, CSIR-IIP, for his constant motivation and support for this study, and for providing necessary infrastructure. Authors also acknowledge CSIR for providing necessary funding through 12 Five Year Plan Project No. CSC-0116/4.

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