Workflow Based on the Combination of Isotopic Tracer Experiments to Investigate Microbial Metabolism of Multiple Nutrient Sources

Podsumowanie

This protocol describes an experimental procedure to quantitatively and comprehensively investigate the metabolism of multiple nutrient sources. This workflow, based on a combination of isotopic tracer experiments and an analytical procedure, allows the fate of consumed nutrients and the metabolic origin of molecules synthetized by microorganisms to be determined.

Streszczenie

Studies in the field of microbiology rely on the implementation of a wide range of methodologies. In particular, the development of appropriate methods substantially contributes to providing extensive knowledge of the metabolism of microorganisms growing in chemically defined media containing unique nitrogen and carbon sources. In contrast, the management through metabolism of multiple nutrient sources, despite their broad presence in natural or industrial environments, remains virtually unexplored. This situation is mainly due to the lack of suitable methodologies, which hinders investigations.

We report an experimental strategy to quantitatively and comprehensively explore how metabolism operates when a nutrient is provided as a mixture of different molecules, i.e., a complex resource. Here, we describe its application for assessing the partitioning of multiple nitrogen sources through the yeast metabolic network. The workflow combines information obtained during stable isotope tracer experiments using selected ¹³C- or ¹⁵N-labeled substrates. It first consists of parallel and reproducible fermentations in the same medium, which includes a mixture of N-containing molecules; however,a selected nitrogen source is labeled each time. A combination of analytical procedures (HPLC, GC-MS) is implemented to assess the labeling patterns of targeted compounds and to quantify the consumption and recovery of substrates in other metabolites. An integrated analysis of the complete dataset provides an overview of the fate of consumed substrates within cells. This approach requires an accurate protocol for the collection of samples–facilitated by a robot-assisted system for online monitoring of fermentations–and the achievement of numerous time-consuming analyses. Despite these constraints, it allowed understanding, for the first time, the partitioning of multiple nitrogen sources throughout the yeast metabolic network. We elucidated the redistribution of nitrogen from more abundant sources toward other N-compounds and determined the metabolic origins of volatile molecules and proteinogenic amino acids.

Wprowadzenie

Understanding how microbial metabolism operates is a key issue for the design of efficient strategies to improve fermentation processes and modulate the production of fermentative compounds. Advances in genomics and functional genomics in these last two decades largely contributed to extending knowledge of the topology of metabolic networks in many microorganisms. Access to this information led to the development of approaches that aim for a comprehensive overview of cellular function¹. These methodologies often rely on a model-based interpretation of measurable parameters. These experimental data include, on one hand, metabolite uptake and production rates and, on the other hand, quantitative intracellular information that is obtained from isotope tracer experiments. These data provide essential information for the deduction of the in vivo activity of different pathways in a defined metabolic network^2,3,4. Currently, the available analytical techniques only enable the accurate detection of labeling patterns of molecules when using a single-element isotope and possibly when co-labeling with two isotopic elements. Moreover, under most growth conditions, the carbon source only consists of one or two-compounds. Consequently, approaches based on ¹³C-isotopic tracers from carbon substrates were widely and successfully applied to develop a complete understanding of carbon metabolic network operations^5,6,7,8.

In contrast, in many natural and industrial environments, the available nitrogen resource that supports microbial growth is often composed of a wide range of molecules. For example, during wine or beer fermentation, nitrogen is provided as a mixture of 18 amino acids and ammonium at variable concentrations⁹. This array of N compounds that are accessible for anabolism makes these complex media conditions greatly different from those commonly used for physiological studies, as the latter are achieved using a unique source of nitrogen, typically ammonium.

Overall, internalized nitrogen compounds may be directly incorporated into proteins or catabolized. The network structure of nitrogen metabolism in many microorganisms, including the yeast Saccharomyces cerevisiae, is very complex in accordance with the diversity of substrates. Schematically, this system is based on the combination of the central core of nitrogen metabolism which catalyzes the interconversion of glutamine, glutamate, and α-ketoglutarate^10,11, with transaminases and deaminases. Through this network, amine groups from ammonium or other amino acids are gathered and α-keto acids released. These intermediates are also synthetized through central carbon metabolism (CCM)^12,13. This large number of branched reactions and intermediates, involved in both the catabolism of exogenous nitrogen sources and the anabolism of proteinogenic amino acids, fulfills the anabolic requirements of the cells. The activity through these different interconnected routes also results in the excretion of metabolites. In particular, α-keto acids may be redirected through the Ehrlich pathway to produce higher alcohols and their acetate ester derivatives¹⁴, which are essential contributors to the sensory profiles of products. Subsequently, how nitrogen metabolism operates plays a key role in biomass production and the formation of volatile molecules (aroma).

The reactions, enzymes, and genes involved in nitrogen metabolism are extensively described in the literature. However, the issue of the distribution of multiple nitrogen sources throughout a metabolic network has not yet been addressed. There are two main reasons that explain this lack of information. First, in view of the important complexity of the nitrogen metabolism network, a large amount of quantitative data is required for a complete understanding of its operation that was unavailable until now. Second, many experimental constraints and limitations of analytical methods prevented the implementation of approaches that were previously used for the elucidation of CCM function.

To overcome these problems, we chose to develop a system-level approach that is based on the reconciliation of data from a series of isotopic tracer experiments. The workflow includes:
- A set of fermentations carried out under the same environmental conditions, while a different selected nutrient source (substrate) is labeled each time.
- A combination of analytical procedures (HPLC, GC-MS) for an accurate determination, at different stages of the fermentation, of the residual concentration of labeled substrate and the concentration and the isotopic enrichment of compounds that are derived from the catabolism of the labeled molecule, including derived biomass.
- A calculation of the mass and isotopic balance for each consumed labeled molecule and a further integrated analysis of the dataset to obtain a global overview of the management of multiple nutrient sources by microorganisms through the determination of flux ratios.

To apply this methodology, attention must be paid to the reproducible behavior of the strain/microorganism between cultures. Furthermore, samples from different cultures must be taken during the same well-defined fermentation progress. In the experimental work reported in this manuscript, a robot-assisted system is used for online monitoring of fermentations to account for these constraints.

Furthermore, it is essential to choose a set of labeled substrates (compound, nature, and position of the labeling) that is appropriate to address the scientific problem of the study. Here, ¹⁵N-labeled ammonium, glutamine, and arginine were selected as the three major nitrogen sources found in grape juice. This allowed assessing the pattern of nitrogen redistribution from consumed compounds to the proteinogenic amino acids. We also aimed to investigate the fate of the carbon backbone of the consumed amino acids and their contribution to the production of volatile molecules. To meet this objective, uniformly ¹³C-labeled leucine, isoleucine, threonine, and valine were included in the study as amino acids that are derived from major intermediates of the Ehrlich pathway.

Overall, we quantitatively explored how yeast manages a complex nitrogen resource by redistributing exogenous nitrogen sources to fulfill its anabolic requirements throughout fermentation while additionally removing the excess of carbon precursors as volatile molecules. The experimental procedure reported in this paper can be applied to investigate other multiple nutrient sources used by any other microorganism. It appears to be an appropriate approach for the analysis of the impact of genetic background or environmental conditions on the metabolic behavior of microorganisms.

Protokół

1. Fermentation and Sampling

1. Preparation of media and fermenters
   NOTE: All the fermentations are carried out in parallel, using the same strain and in the same chemically defined synthetic medium (SM, composition provided in Table 1), which includes a mixture of ammonium and amino acids as nitrogen sources¹⁵. For each fermentation, a single nitrogen compound is provided exclusively in a uniformly labeled ¹³C or ¹⁵N form (100%), while the others remain unlabeled. For each labeled nitrogen source that is used in the set of experiments (here: ¹⁵NH₄, U-¹⁵N4-Arg, U-¹⁵N2-Gln, U-¹³C6-Leu, U-¹³C5-Val, U-¹³C6-Ile, U-¹³C4-Thr), two fermenters are prepared. For each condition, duplicate fermentation is performed using only unlabeled molecules (7 control fermentations).
   1. For each N-source to be studied, prepare 500 mL of SM medium that contains all the nitrogen sources listed in Table 1, with the exception of the compound to be used in 100% labeled form.
      NOTE: The labeled molecule is added in the next steps.
   2. Pasteurize each medium in a 1 L flask (10 min, 100 °C) containing a magnetic stirring bar. Weigh the appropriate amount of labeled molecule to reach the final concentration that is reported in Table 1 and dissolve it in the medium.
   3. Sterilize the medium using a disposable vacuum filtration system (cellulose acetate membrane, 0.22 µm). Using a sterile measuring cylinder, divide the medium between two pre-sterilized fermenters (250 mL) that contain a magnetic stirring bar and are equipped with fermentation locks to avoid the entry of oxygen but allow the release of CO₂.
   4. Heat the fermentation flasks to 28 °C by placing them in the incubation room for 1 night (temperature set at 28 °C).
2. Inoculation and monitoring of fermentations
   1. Grow S. cerevisiae strain in sterile tubes containing 10 mL of YPD medium at 28 °C with shaking (150 rpm) for 12 h. Then, pipet 1 mL of YPD preculture and transfer it to 10 mL of SM medium (in 15 mL sterile tubes). Incubate the culture for 12 h at 28 °C with shaking (150 rpm).
   2. Under laminar flow, collect a preculture aliquot and quantify the cell population using an electronic particle counter that is fitted with a 100 µm aperture. Centrifuge the preculture (2,000 x g, 15 min, 4 °C) and suspend the pellet in an appropriate volume of sterile water to obtain a final concentration of 2.5 x 10⁸ cells/mL. Inoculate each fermenter with 1 mL of the cell suspension.
      NOTE: The robotic system used to monitor the fermentation progress is described in Figure 1.
   3. Prepare the fermentation platform by installing the fermenters in the support guides that are properly placed on the 21-position stirring plates and set the stirring rate at 270 rpm. To start the on-line monitoring of each fermentation, launch the robot-control application, then click the "start assay" button and select the fermentation volume to be carried out (300 mL).
   4. The displayed interface permits the indication of the number and the position of fermenters on the platform. To ensure this occurs, right click on the slot location and choose "enable" to activate the monitoring of the fermenter located at this position.
   5. Initialize the calculation software, permanently running on the system, before starting the weight acquisition. Click on the "Initialiser" button and validate with "ok". Click on the "Start button" of the robot-control application to start the weight acquisitions.
3. Sampling Procedure
   NOTE: For each fermenter, samples are taken when the CO₂ production (value shown on-line on the computer running the calculation software) reaches the required set-point: 5, 10, 40, and 90 g/L in this study.
   1. Sampling procedure for cultures with labeled compounds.
      1. Centrifuge two 6 mL samples (2,000 x g, 5 min, 4 °C). Save and store the frozen supernatants in two aliquots at -80 °C. Wash the pellets twice with 5 mL distilled water and store at -80 °C for the measurement of isotopic enrichments.
   2. Sampling procedure for cultures without labeled compounds
      1. Harvest 10 mL of culture, which will be used for dry weight determination. Pellet the cells from two 10 mL samples by centrifugation (2,000 x g, 5 min, 4 °C). Wash the pellets twice with 10 mL of distilled water and store them at -80 °C for the determination of protein and amino acid content.

2. Quantification of Consumed Nitrogen Sources

1. Enzymatic determination of residual ammonia concentrations
   NOTE: The determination of ammonia concentration in supernatants is carried out using a commercial enzyme-based kit; all the reagents are provided by the manufacturer.
   1. Prepare a standard ammonia solution (61.4 mg/L) by dissolving 25 mg of precisely weighed (NH₄)₂SO₄ in a 100 mL volumetric flask.
   2. To fulfill the manufacturer's instructions, perform a 1:2 dilution of the samples that were taken before fermentation and at 5 g/L of CO₂ released. Adjust the pH of the samples to approximately 8 by adding 1 M KOH. Take note of the added volume and take it into account in the dilution factor.
   3. In 4 mL spectrophotometer cuvettes, mix 100 µL of sample (diluted if necessary), distilled water or standard ammonia solution with 2 mL of reagent 1 (0.75 mM ADP and 30 U/mL glutamate dehydrogenase in pH 7.8 buffer) and 500 µL of reagent 2 (1.3 mM NADH). Incubate for 15 min at room temperature and read NADH absorbance at 340 nm (A1).
   4. Add 500 µL of reagent 3 (60 mM α-ketoglutarate in pH 8 buffer), incubate the sample for 20 min at room temperature, and read the NADH absorbance at 340 nm (A2).
   5. Calculate ammonia concentration using:
      C_ammonia (g/L) = 0.083 x [(0.839 x A1 -A2)_sample- (0.839 x A1 -A2)_{distilled water}]
   6. Check that the correct concentration is obtained with the standard solution.
2. Chromatographic determination of residual amino acid concentrations
   NOTE: The determination of amino acid concentrations in supernatants is achieved using a dedicated amino acid analysis system that is based on ion-exchange chromatography with post column derivatization of N-compounds with ninhydrin, which allows their colorimetric detection.
   1. Prepare a reference solution by adding 200 µL of a commercial mixture of neutral and acidic amino acids, 200 µL of a commercial mixture of basic amino acids, and 200 µL of 2.5 mM glutamine to 400 µL of 200 mM lithium citrate buffer, pH 2.2. This chemically defined reference solution is treated as a sample.
   2. Add 200 µL of 25% (w/v) sulfosalicylic acid solution that contains 2.5 mM norleucine (internal standard) to 800 µL of sample to remove molecules with high molecular weights. Incubate for 1 h at 4 °C, centrifuge (3,000 x g, 10 min, 4 °C) and filter through a 0.22-µm pore-size nitrocellulose membrane (syringe system).
   3. In the programmer software, click on the button "Run" to begin the liquid chromatography (LC) analyses with the analyzer equipped with a cation-exchange column (lithium form). Elute the amino acids with successive lithium buffers to create both a pH gradient and a gradient in counter-ion concentration in combination with a temperature gradient (Table 2).
   4. Quantify the nitrogen compounds after ninhydrin derivatization by a spectrophotometric detector at 570 nm (purple coloration: reaction between ninhydrin and amine group of amino acids) and 440 nm (yellow coloration: reaction between ninhydrin and imine group of proline).
   5. Perform a single-point internal calibration using the reference solution and norleucine as an internal standard to calculate the concentrations of amino acids in the samples using the manufacturer's software.

3. Quantification of Proteinogenic Amino Acids

1. Measurement of dry cell weight
   1. Filter 10 mL of culture through a nitrocellulose filter (pore size 0.45 µm) that is pre-weighed in an aluminum cup, using a vacuum device. Wash twice with 50 mL of distilled water.
   2. Place the filter in the aluminum cup and dry in a heat oven at 105 °C for 48 h (until no further change in weight is observed) before reweighing the filter in the cup. Calculate the weight difference.
   3. Calculate the average of at least 3 independent measurements to accurately determine the dry cell weight of the yeast culture.
2. Quantification of protein content of cells
   NOTE: The quantification of the protein fraction of the cells is performed at least in triplicate using unlabeled cell pellets that were obtained as described in section 1.3.2.
   1. Extract proteins by addition of 1 mL of DMSO solution (50 % v/v) to frozen pellets and incubate at 105 °C for 1 h in a dry heat oven.
   2. Quantify the protein content in the DMSO extracts using the biochemical colorimetric assay that is based on the reduction by proteins of Cu⁺⁺ into Cu⁺ ions that are further precipitated by bicinchoninic acid in a blue complex (BCA assay).
3. Determination of the relative contributions of amino acids within proteins
   NOTE: The profile of proteinogenic amino acids is determined at least in triplicate from unlabeled cell pellets (1.3.2.).
   1. Prepare an oxidized extract by suspending the cell pellet in 200 µL of performic acid (90% formic acid, 10% hydrogen peroxide). Incubate for 4 h at 4 °C and stop the reaction by the addition of 33.6 mg sodium sulfate.
      NOTE: The oxidation step is required to convert cysteine and methionine into methionine sulfone and cysteic acid, which will be further quantified by ion-exchange chromatography. However, some amino acids (tyrosine, phenylalanine, histidine, and arginine) are denatured during oxidation treatment. Consequently, two hydrolysates (with and without oxidation) are prepared.
   2. Add 800 µL of 6N HCl to cell pellets or oxidized extract and incubate the sample in a hermetically sealed glass tube for 16 h at 110 °C in a dry heat oven. Add 200 µL of 2.5 mM norleucine and remove HCl with a stream of nitrogen. Wash (resuspending the dried extract and then removing the liquid with a nitrogen stream) twice with 800 µL of distilled water and then with 800 µL of ethanol. Take up in 800 µL of 200 mM lithium acetate buffer, pH 2.2.
      NOTE: Attention should be paid to the incubation time for the hydrolysis as some amino acids are not stable under acidic conditions. The tryptophan fraction in protein is estimated from data found in the literature¹⁶, as this amino acid is entirely denatured during HCl hydrolysis.
   3. Prepare a hydrolysate standard for the single-point internal calibration. Add 160 µL of a commercial solution of hydrolyzed amino acids to 840 µL of 200 mM lithium acetate buffer, pH 2.2, that contains 625 µM methionine sulfone, 625 µM cysteic acid, and 625 µM norleucine.
   4. Determine the relative concentrations of amino acids within proteins using the chromatographic method described in section 2.2.
4. Calculations
   1. Calculate the weight percentage of each amino acid in proteins by dividing the measured amount of each amino acid (mg/L) by the total amount of amino acid that was measured in the protein extract (sum in mg/L).
   2. Multiply this percentage by the concentration of proteins in the culture (mg/L), i.e., the product between the protein content of the biomass and the dry weight, to assess the concentration of each proteinogenic amino acid in the culture (mg/L).

4. Measurement of Isotopic Enrichment of Proteinogenic Amino Acids

NOTE: For the measurement of isotopic enrichment of proteinogenic amino acids, use the labeled cell pellets. Three different agents are used for the derivatization step to quantify the isotopic enrichment of amino acids. The intensities of cluster ions are measured to estimate the labeling patterns of the amino acids. The signal from each cluster ion corresponds to the abundance of the mass isotopomers (m₀ = without labeling, m₊₁ = 1 labeled atom, …) of an amino acid fragment. An example of a chromatogram that is obtained after the DMADMF procedure is provided in Figure 2.

1. Biomass hydrolysis
   1. Hydrolyze the cell pellets (corresponding to 1-2 mg of dried biomass) by adding 1.2 mL of 6 M HCl and incubating the sample for 16 h at 105 °C in tightly closed glass tubes in a dry heat oven.
   2. Add 1.2 mL of distilled water and centrifuge at 3,000 x g for 5 min to remove cellular debris. Distribute the supernatant into six 400 µL fractions in open glass tubes. Dry the fractions in a heat oven at 105 °C until they reach the consistency of syrup (4-5 h).
2. Ethylchloroformate (ECF) derivatization
   1. Dissolve the dried hydrolysate in 200 µL of 20 mM HCl; then, add 133 µL of pyridine:ethanol (1:4). Add 50 µL of ECF to derivatize the amino acids and wait until all CO₂ has been released. Transfer the mixture to centrifuge tubes that contain 500 µL of dichloromethane to extract the derivatized compounds.
   2. Vortex the tubes for 10 s and centrifuge them for 4 min at 10,000 x g; collect the lower organic phase with a Pasteur pipet and transfer to GC vials that contain conical glass inserts so that the samples may be directly injected into the GC/MS instrument.
3. (N,N)-Dimethylformamide dimethyl acetal (DMFDMA) derivatization.
   1. Dissolve the dried hydrolysate in 50 µL of methanol and 200 µL of acetonitrile. Add 300 µL of DMFDMA. Vortex the tube and transfer the samples to GC autosampler vials that contain conical glass inserts.
4. N,O-Bis(trimethylsilyl)trifluoroacetamide (BSTFA) derivatization
   1. Suspend the hydrolysate in 200 µL of acetonitrile. Add 200 µL of BSTFA, hermetically close the glass tube and incubate for 4 h at 135 °C before transferring the extract directly to GC vials.
5. GC-MS analysis
   1. Analyze samples with a gas chromatograph that is equipped with an autosampler injector and is coupled to a mass spectrometer.
      1. Use instrument-specific software to control the instrument and analyze the chromatograms. In the "Sequence" menu, click the "Sample Log Table" to create the sample list, and click the "Run" button to start the injections.
         NOTE: The gas chromatograph is fitted with a 30 m x 0.25 mm apolar silica capillary column with a 0.15 μm film thickness. Set the mass spectrometer quadrupole temperature at 150 °C and hold the transfer line at 250 °C for all the analyses. Three analytical programs, each one specific to each derivatization agent, are used.
      2. ECF derivatives: Use helium as the mobile phase with a flow of 1.2 mL/min. Set the temperature of the inlet at 230 °C and that of the source at 250 °C. Program the autosampler to inject 1 µL of samples with a split ratio of 3:1. Run the analyses, gradually increasing the oven temperature as follows: 130 °C for 3 min; gradient of 15 °C/min to 260 °C; maintain temperature at 260 °C for 20 min.
      3. DMFDMA derivatives: Use helium as the mobile phase with a constant flow of 1.2 mL/min. Set the temperature of the inlet at 230 °C and that of the source at 250 °C. Program the autosampler to inject 1 µL of samples with a split ratio of 3:1. Run the analyses, gradually increasing the oven temperature as follows: 60 °C for 1 min; gradient of 20 °C/min to 130 °C; second gradient of 4 °C/min to 260 °C; maintain temperature at 260 °C for 10 min.
      4. BSTFA derivatives: Use helium as the mobile phase with a constant flow of 1.2 mL/min. Set the temperature of the inlet at 275 °C and that of the source at 300 °C. Run the analyses (injection: 1 µL), gradually increasing the oven temperature as follows: 110 °C for 1 min; first gradient of 2 °C/min to 154 °C; second gradient of 5 °C/min to 300 °C; maintain temperature at 300 °C for 10 min.
      5. Detection procedure: For each mode of derivatization, inject a sample (1 µL) in SCAN mode with positive electron impact ionization at 70 eV and take note of the retention time of each amino acid.
      6. Use these values to define the time windows throughout the chromatogram and for the different selected ions, which are characteristic of each amino acid and listed in Table 3; these values should be included for each amino acid. Include this information in the SIM detection program and run the analyses in SIM mode with positive electron impact ionization at 70 eV.
   2. Collect the outcomes of the analyses; namely, for each amino acid, record a cluster of intensities that correspond to its different mass isotopomers. Process the data using the dedicatedsoftware¹⁷ to correct for natural labeling and calculate the isotopic enrichment of the proteinogenic amino acids (defined as the labeled fraction of an amino acid with respect to its total amount in the protein samples).
      NOTE: The isotopic enrichment of a molecule (I.E.), expressed as a percentage, is calculated dividing the sum of the corrected intensities of the mass isotopomers with labeling (m₁, m₂, …m_n) by the sum of the corrected intensities of all the mass isotopomers (m₀, m₁, m₂,… m_n):
      I. E. = (m₁ + m₂ + …+ m_n) / (m₀ + m₁+ m₂ + …+ m_n)

5. Quantification and Isotopic Enrichment of Volatile Compounds

1. Extraction of labeled volatile compounds
   1. Add 10 µL of deuterated internal standards to 5 mL of supernatant (final concentration of deuterated compounds: 100 µg/L) in a 15 mL glass tube. Add 1 mL of dichloromethane, tightly close the tubes and shake them on a rocking platform for 20 min. Centrifuge for 5 min at 3,000 x g and collect the organic lower phase in a 15 mL glass tube. Repeat the dichloromethane extraction.
   2. Dry the organic extract over 500 mg of anhydrous sodium sulfate and collect the liquid phase with a Pasteur pipet. Concentrate the extract by a factor of four under nitrogen flux and transfer it to a GC autosampler vial.
2. GC-MS quantification of volatile compounds
   1. Equip the gas chromatograph with a 30 m x 0.25 mm fused silica capillary column with 0.25 μm film thickness and apply a constant helium flow of 1.0 mL/min. Hold the injector and the transfer line at 250 °C.
   2. Inject 2 µL of sample with a split ratio of 10:1 and separate the extracted volatile molecules using the following oven temperature profile: hold the temperature for 3 min at 40 °C, increase it by 4 °C/min up to 220 °C and then hold the oven at 220 °C for 20 min.
   3. Detect the compounds using a mass spectrometer with its source temperature set at 230 °C and its mass spectrometer quadrupole temperature set at 150 °C. Record the mass spectra in Selected Ion Monitoring (SIM) mode with positive electron impact ionization at 70 eV and using the ion clusters specific to the volatile compounds that are reported in Table 4.
   4. Use an external 7-point calibration to quantify the concentrations of volatile molecules from the sums of the intensities of the corresponding ion cluster. Prepare stock solutions of each compound (10 g/L) in 100% ethanol. Then, prepare standard solutions for each class of volatile molecules (ethyl esters, acetates, alcohols, and acids) by mixing stock solutions. Finally, dilute different amounts of the standard solutions in a 12% hydroalcoholic solution containing 5 g/L tartaric acid with the pH adjusted to 3.3 to prepare calibration solutions.
   5. In parallel, correct for the natural labeling of the intensities of each ion cluster and calculate the isotopic enrichment of volatile compounds, which is defined as the labeled fraction of the molecules and is expressed as a percentage using the dedicated software¹⁷.

6. Calculations for an Integrated Analysis of the Dataset

1. Collection of the raw data
   1. Using the spreadsheets shown in Tables 5, 6, 7, and 8, enter the raw data values that correspond to the concentration of extracellular amino acids, cell dry weight, protein content of cells, concentration of volatile molecules, and isotopic enrichment of proteinogenic amino acids and volatile molecules.
      NOTE: The data shown in tables are expressed in mM. All the results are also expressed in mg/L by multiplying the values in mM by the molecular weight of each molecule or in mg N/L by multiplying the millimolar concentration of a proteinogenic amino acid by the atomic mass of nitrogen (14 u) and by the number of nitrogen atoms that are provided by the catabolism of this molecule.
   2. Calculate the mass percentage of each amino acid in proteins by dividing its amount in mg/L in the hydrolysate by the total amount of amino acids (their sum in mg/L).
   3. Calculate means, standard deviations, and standard errors of the mean from the data that were obtained in the independent experiments.
   4. Calculate the proteinogenic concentration (mg/L) for each amino acid by multiplying the percentage of this amino acid in proteins (mg aa/g proteins) by the protein fraction in the biomass (g proteins/g DW) and the dry weight content (biomass production) in the medium (g DW/L).
2. ¹⁵N isotopic tracer experiments
   1. Using the spreadsheets that are presented in Table 9, calculate the labeled and unlabeled fractions of nitrogen that are present in the proteinogenic amino acids (expressed in mg N/L) from their total concentrations (expressed in mg N/L) and their isotopic enrichments. For each amino acid, the labeled fraction corresponds to the product between its total concentration and its isotopic enrichment, and the unlabeled part is the difference between the total and the labeled amounts.
   2. Then, determine the fraction of total nitrogen in proteins that is contained in the proteinogenic amino acids quantified in this study by summing the total amount of Ala, Gly, Val, Asp, Phe, Leu, Ile, Thr, Ser, Pro, Lys, His, Glu and Arg (in mg N/L) and dividing the total amount of nitrogen contained in proteins by this sum.
   3. Calculate the nitrogen provided by arginine, glutamine or ammonium that was recovered in the proteinogenic acids quantified in this study by summing the labeled fraction (in mg N/L) of proteinogenic amino acids that were quantified in the study (Ala, Gly, Val, Asp, Phe, Leu, Ile, Thr, Ser, Pro, Lys, His, Glu, and Arg) during experiments in the presence of ¹⁵N-labeled arginine, glutamine, or ammonium and dividing this labeled-nitrogen fraction by the total amount of nitrogen in the quantified proteinogenic amino acids.
   4. Assess the contribution of the 3 most abundant amino acids to the intracellular pool of nitrogen used for de novo biosynthesis by combining data from the ¹³C and ¹⁵N isotope tracer experiments (spreadsheet in Table 7).
   5. From the total amount (expressed in mM) of proteinogenic Val, Leu, Ile, or Thr, deduct the part derived from the direct incorporation of consumed compounds (¹³C experiments) and the part that was de novo synthetized using nitrogen from the 3 major sources in order to assess the fraction that was de novo synthetized using nitrogen from the other amino acids.
   6. Then, calculate the ratio of the amount of amino acid de novo synthetized using nitrogen provided by Gln, Arg, and NH₄⁺ (sum expressed in mM) to the total amount of proteinogenic amino acids (in mM) to quantify the contribution of arginine, glutamine, and ammonium to the intracellular nitrogen pool.
3. ¹³C isotopic tracer experiments
   1. Calculate the labeled and unlabeled fractions of the proteinogenic amino acids from concentrations expressed in mM and isotopic enrichments of proteinogenic amino acids that were obtained during experiments in the presence of ¹³C-labeled Leu, Val, Ile or Thr. (see 6.2.1, Table 10).
   2. Calculate the labeled and unlabeled fractions of volatile compounds from concentrations expressed in mM and isotopic enrichments of volatile compounds that were obtained during experiments in the presence of ¹³C-labeled Leu, Val, Ile, or Thr (Table 10).

Wyniki

Figure 3 presents a schematic diagram of the workflow that was implemented to investigate the management by yeast of the multiple nitrogen sources that are found during wine fermentation.
For different points of sampling, the biological parameters–growth characteristics, nitrogen consumption patterns, and the profile of proteinogenic amino acids–show a high reproducibility among fermentations (Figure 4). This co...

Dyskusje

Quantifying the partitioning of compounds through metabolic networks using isotopic tracer experiments is a promising approach for understanding the operation of microbial metabolism. This methodology, while successfully applied with one or two labeled substrates, cannot currently be implemented to study metabolism of various sources using multiple labeled elemental isotopes (i.e., more than two substrates). Indeed, the available analytical techniques enable the accurate determination of the labeling patterns of...

Materiały

Name	Company	Catalog Number	Comments
D-Glucose	PanReac	141341.0416
D-Fructose	PanReac	142728.0416
DL-Malic acid	Sigma Aldrich	M0875
Citric acid monohydrate	Sigma Aldrich	C7129
Potassium phosphate monobasic	Sigma Aldrich	P5379
Potassium sulfate	Sigma Aldrich	P0772
Magnesium sulfate heptahydrate	Sigma Aldrich	230391
Calcium chloride dihydrate	Sigma Aldrich	C7902
Sodium chloride	Sigma Aldrich	S9625
Ammonium chloride	Sigma Aldrich	A4514
Sodium hydroxide	Sigma Aldrich	71690
Manganese sulfate monohydrate	Sigma Aldrich	M7634
Zinc sulfate heptahydrate	Sigma Aldrich	Z4750
Copper (II) sulfate pentahydrate	Sigma Aldrich	C7631
Potassium iodine	Sigma Aldrich	P4286
Cobalt (II) chloride hexahydrate	Sigma Aldrich	C3169
Boric acid	Sigma Aldrich	B7660
Ammonium heptamolybdate	Sigma Aldrich	A7302
Myo-inositol	Sigma Aldrich	I5125
D-Pantothenic acid hemicalcium salt	Sigma Aldrich	21210
Thiamine, hydrochloride	Sigma Aldrich	T4625
Nicotinic acid	Sigma Aldrich	N4126
Pyridoxine	Sigma Aldrich	P5669
Biotine	Sigma Aldrich	B4501
Ergostérol	Sigma Aldrich	E6510
Tween 80	Sigma Aldrich	P1754
Ethanol absolute	VWR Chemicals	101074F
Iron (III) chloride hexahydrate	Sigma Aldrich	236489
L-Aspartic acid	Sigma Aldrich	A9256
L-Glutamic acid	Sigma Aldrich	G1251
L-Alanine	Sigma Aldrich	A7627
L-Arginine	Sigma Aldrich	A5006
L-Cysteine	Sigma Aldrich	C7352
L-Glutamine	Sigma Aldrich	G3126
Glycine	Sigma Aldrich	G7126
L-Histidine	Sigma Aldrich	H8000
L-Isoleucine	Sigma Aldrich	I2752
L-Leucine	Sigma Aldrich	L8000
L-Lysine	Sigma Aldrich	L5501
L-Methionine	Sigma Aldrich	M9625
L-Phenylalanine	Sigma Aldrich	P2126
L-Proline	Sigma Aldrich	P0380
L-Serine	Sigma Aldrich	S4500
L-Threonine	Sigma Aldrich	T8625
L-Tryptophane	Sigma Aldrich	T0254
L-Tyrosine	Sigma Aldrich	T3754
L-Valine	Sigma Aldrich	V0500
13C5-L-Valine	Eurisotop	CLM-2249-H-0.25
13C6-L-Leucine	Eurisotop	CLM-2262-H-0.25
15N-Ammonium chloride	Eurisotop	NLM-467-1
ALPHA-15N-L-Glutamine	Eurisotop	NLM-1016-1
U-15N4-L-Arginine	Eurisotop	NLM-396-PK
Ethyl acetate	Sigma Aldrich	270989
Ethyl propanoate	Sigma Aldrich	112305
Ethyl 2-methylpropanoate	Sigma Aldrich	246085
Ethyl butanoate	Sigma Aldrich	E15701
Ethyl 2-methylbutanoate	Sigma Aldrich	306886
Ethyl 3-methylbutanoate	Sigma Aldrich	8.08541.0250
Ethyl hexanoate	Sigma Aldrich	148962
Ethyl octanoate	Sigma Aldrich	W244910
Ethyl decanoate	Sigma Aldrich	W243205
Ethyl dodecanoate	Sigma Aldrich	W244112
Ethyl lactate	Sigma Aldrich	W244015
Diethyl succinate	Sigma Aldrich	W237701
2-methylpropyl acetate	Sigma Aldrich	W217514
2-methylbutyl acetate	Sigma Aldrich	W364401
3-methyl butyl acetate	Sigma Aldrich	287725
2-phenylethyl acetate	Sigma Aldrich	290580
2-methylpropanol	Sigma Aldrich	294829
2-methylbutanol	Sigma Aldrich	133051
3-methylbutanol	Sigma Aldrich	309435
Hexanol	Sigma Aldrich	128570
2-phenylethanol	Sigma Aldrich	77861
Propanoic acid	Sigma Aldrich	94425
Butanoic acid	Sigma Aldrich	19215
2-methylpropanoic acid	Sigma Aldrich	58360
2-methylbutanoic acid	Sigma Aldrich	193070
3-methylbutanoic acid	Sigma Aldrich	W310212
Hexanoic acid	Sigma Aldrich	153745
Octanoic acid	Sigma Aldrich	W279900
Decanoic acid	Sigma Aldrich	W236403
Dodecanoic acid	Sigma Aldrich	L556
Fermentor 1L	Legallais	AT1357	Fermenter handmade for fermentation
Disposable vacuum filtration system	Dominique Deutscher	029311
Fermenters (250 ml)	Legallais	AT1352	Fermenter handmade for fermentation
Sterile tubes	Sarstedt	62.554.502
Fermentation locks	Legallais	AT1356	Fermetation locks handmade for fermentation
BactoYeast Extract	Becton, Dickinson and Company	212750
BactoPeptone	Becton, Dickinson and Company	211677
Incubator shaker	Infors HT
Particle Counter	Beckman Coulter	6605697	Multisizer 3 Coulter Counter
Centrifuge	Jouan		GR412
Plate Butler Robotic system	Lab Services BV	PF0X-MA	Automatic instrument
Plate Butler Software	Lab Services BV		Robot monitor software
RobView			In-house developed calculation software
My SQL			International source database
Cimarec i Telesystem Multipoint Stirrers	Thermo Fisher Scientific	50088009	String Drive 60
BenchBlotter platform rocker	Dutscher	60903
Ammonia enzymatic kit	R-Biopharm AG	5390
Spectrophotometer cuvettes	VWR	634-0678
Spectrophotometer UviLine 9400	Secomam
Amino acids standards physiological - acidics and neutrals	Sigma Aldrich	A6407
Amino acids standards physiological - basics	Sigma Aldrich	A6282
Citrate lithium buffers - Ultra ninhydrin reagent	Biochrom	BC80-6000-06
Sulfosalycilic acid	Sigma Aldrich	S2130
Norleucine	Sigma Aldrich	N1398
Biochrom 30 AAA	Biochrom
EZChrom Elite	Biochrom		Instrument control and Data analysis software
Ultropac 8 resin Lithium	Biochrom	BC80-6002-47	Lithium High Resolution Physiological Column
Filter Millex GV	Merck Millipore	SLGVX13NL	Millex GV 13mm (pore size 0.22 µm)
Membrane filter PALL	VWR	514-4157	Supor-450 47mm 0.45µm
Vacuum pump Millivac Mini	Millipore	XF5423050
Aluminium smooth weigh dish 70mm	VWR	611-1380
Precision balance	Mettler		Specifications AE163
Dimethyl sulfoxid dried	Merck	1029310161	(max. 0.025% H2O) SeccoSolv
Combustion oven	Legallais
Pierce BCA protein assay kit	Interchim	UP40840A
Formic acid	Fluka	94318
Hydrogen peroxide	Sigma Aldrich	H1009
Hydrochloric Acid Fuming 37% Emsure	Merck	1003171000	Grade ACS,ISO,Reag. Ph Eur
Lithium acetate buffer	Biochrom	80-2038-10
Commercial solution of hydrolyzed amino acids	Sigma Aldrich	AAS18
L-Methionine sulfone	Sigma Aldrich	M0876
L-Cysteic acid monohydrate	Sigma Aldrich	30170
Pyrex glass culture tubes	Sigma Aldrich	Z653586
Pyridine	Acros Organics	131780500	99% Extrapure
Ethyl chloroformate	Sigma Aldrich	23131
Dichloromethane	Sigma Aldrich	32222
Vials	Sigma Aldrich	854165
Microinserts for 1.5ml vials	Sigma Aldrich	SU860066
GC/MS	Agilent Technologies	5890 GC/5973 MS
Chemstation	Agilent Technologies		Instrument control and data analysis software
Methanol	Sigma Aldrich	34860	Chromasolv, for HPLC
Acetonitrile	Sigma Aldrich	34998	ChromasolvPlus, for HPLC
N,N-Dimethylformamide dimethyl acetal	Sigma Aldrich	394963
BSTFA	Sigma Aldrich	33024
DB-17MS column	Agilent Technologies	122-4731	30m*0.25mm*0.15µm
Sodium sulfate, anhydrous	Sigma Aldrich	238597
Technical nitrogen	Air products	14629
Zebron ZB-WAX column	Phenomenex	7HG-G007-11	30m*0.25mm*0.25µm
Helium BIP	Air products	26699
Glass Pasteur pipettes	VWR	612-1702