Using Microtiter Dish Radiolabeling for Multiple In Vivo Measurements Of Escherichia coli (p)ppGpp Followed by Thin Layer Chromatography

Summary

The growth of radiolabeled bacterial cultures in microtiter dishes facilitates high throughput sampling that allows multiple technical and biological replicate assays of nucleotide pool abundance, including that of (p)ppGpp. The effects of growth transitions provoked by sources of physiological stress as well as recovery from stress can be monitored.

Abstract

The (p)ppGpp nucleotide functions as a global regulator in bacteria in response to a variety of physical and nutritional stress. It has a rapid onset, in seconds, which leads to accumulation of levels that approach or exceed those of GTP pools. Stress reversal occasions a rapid disappearance of (p)ppGpp, often with a half-life of less than a minute. The presence of (p)ppGpp results in alterations of cellular gene expression and metabolism that counter the damaging effects of stress. Gram-negative and Gram-positive bacteria have different response mechanisms, but both depend on (p)ppGpp concentration. In any event, there is a need to simultaneously monitor many radiolabeled bacterial cultures at time intervals that may vary from 10 seconds to hours during critical stress transition periods. This protocol addresses this technical challenge. The method takes advantage of temperature- and shaker-controlled microtiter dish incubators that allow parallel monitoring of growth (absorbance) and rapid sampling of uniformly phosphate-radiolabeled cultures to resolve and quantitate nucleotide pools by thin-layer chromatography on PEI-cellulose. Small amounts of sample are needed for multiple technical and biological replicates of analyses. Complex growth transitions, such as diauxic growth and rapid (p)ppGpp turnover rates can be quantitatively assessed by this method.

Introduction

The (p)ppGpp second messenger is a global regulator that modulates the expression of a large number of genes, including genes for synthesizing ribosomes and amino acids^1,2. Although initially discovered in Escherichia coli³, (p)ppGpp can be found in both Gram positive and Gram negative bacteria as well as in plant chloroplasts^4,5. For E. coli and other Gram-negative bacteria, (p)ppGpp interacts directly with RNA polymerase at two different sites^6,7,8. In Gram positives, (p)ppGpp inhibits GTP abundance, which is sensed by CodY, a GTP-binding protein with gene-specific DNA recognition motifs that lead to regulation^9,10. (p)ppGpp accumulates in response to starvation for different nutrients and stress conditions, resulting in slow growth and adjustments of gene expression to allow adaptation to stress^11,12.

The net amount of ppGpp accumulated reflects a balance between synthetase and hydrolase activities. In E. coli RelA is a strong synthetase and SpoT is bifunctional, with a strong hydrolase and a weak synthetase, each of which might be regulated differently in a stress dependent manner. The strong RelA synthetase is activated when the availability of codon-specified charged tRNA bound to the ribosomal A site when it fails to keep up with the demands of protein synthesis^13,14,15. The weak SpoT (p)ppGpp synthetase is activated while the strong (p)ppGpp hydrolase is inhibited in response to other stress conditions and through other mechanisms. Under some conditions, proteins such as ACP or Rsd can bind to SpoT, which also change the balance between hydrolysis and synthesis^16,17. In Gram positives, synthesis and hydrolysis reflect a more complex balance between a single RelA SpoT homolog (RSH) protein with strong synthesis and hydrolysis activities as well as smaller hydrolases and/or synthetases¹².

The (p)ppGpp nucleotides were first discovered as unusual ³²P labeled spots that appeared on autoradiograms of thin-layer chromatograms (TLC) during a stringent response induced by amino acid starvation³. More detailed labeling protocols have been reviewed ¹⁸. The protocol described here (Figure 1) is a modification of these protocols that allows monitoring growth of multiple samples on microtiter plates. This facilitates multiple biological and technical estimates of (p)ppGpp abundance changes and was initially developed for studies  of diauxic shifts¹⁹. Labelling of (p)ppGpp with ³²P and detection by TLC also allows measurements of (p)ppGpp degradation rates. Alternative methods have been developed to determine (p)ppGpp levels such as mass spectrometry,  HPLC²⁰, fluorescent chemosensors^21,22, and GFP gene fusions to promoters affected by ppGpp^23,24. Fluorescent chemosensors currently have a limited use due small spectral shifts after binding ppGpp as well as problems distinguishing between ppGpp and pppGpp²¹. This method is efficient to detect (p)ppGpp in vitro, but not in cellular extracts. Methods involving HPLC have been improved²⁰ but require expensive equipment and are not well adapted to high through-put. Finally, GFP fusions can give an estimate of ppGpp dependent activation or inhibition, but do not measure ppGpp itself. While each of these alternative methods are valuable, they require expensive equipment or substantial hands-on time, or they are otherwise not amenable to multiple kinetic sampling and subsequent processing. With the method described here, 96 samples can be applied to six TLC plates in about 20 min (18 samples per plate), resolved by TLC development in less than a couple of hours, with quantitative data obtained after several hours or overnight, depending on labeling intensity.

Protocol

1. Media Preparation

1. For MOPS (3-(N-morpholino)propanesulfonic acid) media²⁵, use 1/10 volume of 10x MOPS salts, 1/100 volume of 100x micronutrients solution, 3 mM sodium phosphate for overnight cultures or 0.2 mM sodium phosphate for uniform labeling with ³²P, 0.2% glucose and 1 µg/mL thiamin (vitamin B1). Add amino acids at 40 µg/mL if required.
   1. For MOPS salts, use 400 mM MOPS, 40 mM Tricine, 0.1 mM FeSO₄, 95 mM NH₄Cl, 2.6 mM K₂SO₄, 5 µM CaCl₂, 10.56 mM MgCl₂, and 500 mM NaCl. Add the different components in the order written to avoid precipitation. Adjust to pH 7.4 with KOH and sterilize by filtration.
   2. For 100x micronutrients solution, use 3 µM (NH₄)₆(MO₇)₂₄, 0.4 mM H₃BO₄, 30 µM CoCl₂, 10 µM CuSO₄, 80 µM MnCl₂, and 10 µM ZnSO₄. Sterilize by autoclaving.
   3. For glucose (20%) and sodium phosphate (300 mM) solutions, sterilize as separate 100x stocks by autoclaving. Sterilize 100x stocks of thiamine and amino acid mixtures by filtration. Prepare fresh media from sterile stock solutions for each experiment.

2. Labelling with ³²P

1. Grow overnight cultures in MOPS media with 3 mM sodium phosphate.
2. In a 24 well plate, add 550 µL of MOPS media containing 0.2 mM sodium phosphate carrier and 30 µL of each bacterial inoculum (dilution 1/20). This will produce an initial inoculum of OD_600nm 0.1. Use one well with fresh media as a sterility control.
3. Place the plate on a shaking incubator at 37 °C shaking at 900 rpm for 30 min. Cultures are heated from below and shaking provides aeration. Attach the plate firmly with tape to avoid tilting or spills. Growth can be monitored with a replicate plate in parallel in media lacking ³²P using a plate reader and incubating under the same conditions.
4. Add 100 µCi to each well of ³²P orthophosphate (20 µL from a 5 mCi/mL stock).
   NOTE: The amount of radioactivity can also be adjusted to meet experimental needs. For low basal levels 100 µCi with 0.2 mM carrier phosphate works well, but for measuring (p)ppGpp levels that are expected to become equivalent to GTP pools, label can be dropped to 25 or 50 µCi. Lowering carrier phosphate below 0.2 mM is not recommended to avoid phosphate levels becoming limiting for growth.
   CAUTION: ³²P is a β emitting isotope so use proper shielding specified for safety. All radioactive material must be properly disposed taking all the possible precautions.
5. Grow in shaking incubator for 1 to 2 doublings (1 h or more) to allow external label to largely equilibrate with intracellular nucleotide pools before inducing stress.

3. Induction of Stress or Starvation

1. Induce stress using a method of your choosing, depending on the sort of stress studied, e.g. adding metabolic pathway inhibitors, changing temperature, exhausting required nutrients, shifting osmolarity shifts, inducing oxidative stress, adding toxins, etc.
   1. For example, add 100 µg/mL L-valine to induce isoleucine starvation in E. coli K-12 strains. Increased levels of ppGpp will be observed after 5 minutes of induction.

4. Sampling and ppGpp Extraction

1. Add 20 µL of each labelled cell sample to a 0.2 mL PCR tube containing 20 µL of ice cold 6 M Formic acid.
2. Immediately place the samples in dry ice.
3. Enhance cellular extraction efficiency by 3 cycles of freezing and thawing.
4. Just before spotting PEI cellulose thin layer chromatograms, centrifuge samples for 1 min at maximum speed to pellet cell debris to avoid spotting it on chromatograms.

5. Thin-layer Chromatography

1. With a soft pencil, mark an origin line 1 cm from the edge of the 20 cm x 20 cm PEI-Cellulose TLC plate that has had 5 cm removed from the top with scissors. Apply 5 µL as a droplet in the PEI surface for each sample. Begin ascending development without allowing this spot to dry, which improve resolution by minimizing streaking.
2. Do ascending development in a tank with a layer of 1.5 M KH₂PO₄ (pH 3.4) solution shallow enough so that liquid does not touch the origin sample spot. Cover the tank with an air-tight seal and allow liquid ascent to the top of the trimmed sheet, 15 cm. To achieve pH 3.4 for a 1.5 M KH₂PO₄ solution, it is necessary adjust the pH by addition of H₃PO₄.
3. Remove the fully developed chromatogram and air dry at room temperature.
4. Cut and discard the top (pH front) portion of the chromatogram containing the free ³²P into radioactive waste. This portion is represented in yellow color in Figure 2 and easily visualized under UV light. If measuring only (p)ppGpp nucleotides that migrate slower than GTP, it is recommended to run a UV-visible GTP standard and then cut and discard a larger upper portion (anything above GTP, as shown in Figure 2).
5. Expose autoradiographic films overnight with a phosphor screen.
6. Develop the film. Capture and quantitate the phosphor screen signal with a phosphoimager.

6. Quantitation of (p)ppGpp

1. Quantitate radioactive spots with Image J^26,27.
   NOTE: The amount of (p)ppGpp can be normalized to total amount of G nucleotides observed in each sample (Figure 2). If the amount of background is homogeneous, a single blank (box 4 from Figure 2) can be subtracted to correct for background. Total G is the sum of GTP + ppGpp + pppGpp detected. This normalization assumes that GMP and GDP levels are negligible, which is true for E. coli. The ratio of a given nucleotide to total G provides an important way to correct for variations of applied sample volume.

7. Measurement of the Rate of ppGpp Decay

NOTE: A modification of this protocol allows measurements of ppGpp decay rates.

1. After provoking stress or starvation for a time sufficient to allow ppGpp accumulation (step 3), reverse the stress in order to block continued ppGpp synthesis, which allows detection of hydrolytic rates. The procedure for reversal will depend on the stress. For example, add 200 µg/mL of chloramphenicol to reverse any amino acid starvation.
2. Decay rates are usually rapid but may vary, so take samples every 20-30 s up to 2 min. Process samples as in step 4.
3. Once the TLC is developed (as in step 5) and the levels of ppGpp obtained during the time course, plot residual ppGpp content on a semi-logarithmic plot vs time to allow visualization of zero order rates of decay, as a straight line, and estimation of the ppGpp half-life.

Results

In E. coli K-12 strains, the addition of valine provokes an endogenous starvation of isoleucine, which results an increase of ppGpp levels after 5 min³. Cells grown in MOPS containing all amino acids except for ILV were labeled with ³²P as indicated in Figure 1. Once labelled, 6 µL of 10 mg/mL L-valine (100 µg/mL final concentration) was added to produce isoleucine starvation. Samples were taken 0 and 5 min after the addition of valine. Afte...

Discussion

Achieving near uniform labeling of the cells is a critical step for this protocol. Therefore, the use of defined media, such as MOPS or Tris media, is crucial to allow variation of carrier phosphate concentrations and specific activity. Phosphate buffered media, such as M9 or media A, cannot be used. Most undefined media contain variable amounts of phosphate, such as LB, tryptone and casamino acids. The phosphate isotope ³³P is a weaker emitter that can be substituted for ³²P. Advantages of the subs...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
(NH4)6(MO7)24	Fisher Scientifics	A-674
Autoradiography film	Denville scientific inc.	E3218
CaCl2	J.T.Baker	1-1309
Chloramphenicol	RPI	C61000-25.0
CoCl2	Fisher Scientifics	C-371
CuSO4	J.T.Baker	1843
FeSO4	Fisher Scientifics	I-146
Formic acid	Fisher Biotech	BP1215-500
Glucose	Macron	4912-12
H3BO4	Macron	2549-04
H3PO4	J.T.Baker	0260-02
K2SO4	Sigma	P9458-250G
KH2PO4	Fisher Biotech	BP362-500
L-Valine	Sigma	V-6504
MgCl2	Fisher Scientifics	FL-06-0303
Microplate reader Synergy HT	Biotek	Synergy HT
MnCl2	Sigma	M-9522
MOPS	Sigma	M1254-1KG
Na2HPO4	Mallinckrodt	7892
NaCl	J.T.Baker	3624-01
NaH2PO4	Mallinckrodt	7917
NH4Cl	Sigma	A0171-500G
P-32 radionuclide, orthophosphoric acid in 1 mL water (5 mCi)	Perkin Elmer	NEX053005MC
Storage phosphor screen	Kodak	So230
Thermomixer	Eppendorf	5382000015
Thiamine	Sigma	T-4625
TLC PEI Cellulose F	Merk-Millipore	1.05579.0001
Tricine	RPI	T2400-500.0
Typhoon 9400 imager	GE Healthcare
ZnSO4	Fisher Scientifics	Z-68