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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

We describe a simple method for rapid quantification of inorganic polyphosphate in diverse bacteria, including Gram-negative, Gram-positive, and mycobacterial species.

Abstract

Inorganic polyphosphate (polyP) is a biological polymer found in cells from all domains of life, and is required for virulence and stress response in many bacteria. There are a variety of methods for quantifying polyP in biological materials, many of which are either labor-intensive or insensitive, limiting their usefulness. We present here a streamlined method for polyP quantification in bacteria, using a silica membrane column extraction optimized for rapid processing of multiple samples, digestion of polyP with the polyP-specific exopolyphosphatase ScPPX, and detection of the resulting free phosphate with a sensitive ascorbic acid-based colorimetric assay. This procedure is straightforward, inexpensive, and allows reliable polyP quantification in diverse bacterial species. We present representative polyP quantification from the Gram-negative bacterium (Escherichia coli), the Gram-positive lactic acid bacterium (Lactobacillus reuteri), and the mycobacterial species (Mycobacterium smegmatis). We also include a simple protocol for nickel affinity purification of mg quantities of ScPPX, which is not currently commercially available.

Introduction

Inorganic polyphosphate (polyP) is a linear biopolymer of phosphoanhydride-linked phosphate units that is found in all domains of life1,2,3. In diverse bacteria, polyP is essential for stress response, motility, biofilm formation, cell cycle control, antibiotic resistance, and virulence4,5,6,7,8,9,10,11. Studies....

Protocol

1. Purifying Yeast Exopolyphosphatase (ScPPX)

  1. Transform the E. coli protein overexpression strain BL21(DE3)31 with plasmid pScPPX26 by electroporation32 or chemical transformation33.
  2. Inoculate 1 L of lysogeny broth (LB) containing 100 µg mL-1 ampicillin in a 2 L unbaffled flask with a single colony of BL21(DE3) containing pScPPX2 and incubate overnight at 37 °C without shakin.......

Representative Results

The key steps of the protocol are diagrammed in simplified form in Figure 1.

To demonstrate the use of this protocol with Gram-negative bacteria, wild-type E. coli MG165539 was grown to mid-log phase in LB rich medium at 37 °C with shaking (200 rpm), then rinsed and incubated for an additional 2 h in morpholinopropanesulfonate-buffered (MOPS) minimal medium

Discussion

The protocol described here simplifies and accelerates quantification of polyP levels in diverse bacteria, with a typical set of 24 samples taking about 1.5 h to fully process. This permits rapid screening of samples and analysis of mutant libraries, and simplifies kinetic experiments measuring the accumulation of polyP over time. We have demonstrated that the protocol works effectively on representatives of three different phyla: proteobacteria, firmicutes, and actinobacteria, which are notorious for their resilient, di.......

Acknowledgements

This project was supported by University of Alabama at Birmingham Department of Microbiology startup funds and NIH grant R35GM124590 (to MJG), and NIH grant R01AI121364 (to FW).

....

Materials

NameCompanyCatalog NumberComments
E. coli BL21(DE3)Millipore Sigma69450
plasmid pScPPX2Addgene112877available to academic and other non-profit institutions
LB brothFisher ScientificBP1427-2E. coli growth medium
ampicillinFisher ScientificBP176025
isopropyl β-D-1-thiogalactopyranoside (IPTG)Gold BiotechnologyI2481C
HEPES bufferGold BiotechnologyH-400-1
potassium hydroxide (KOH)Fisher ScientificP250500for adjusting the pH of HEPES-buffered solutions
sodium chloride (NaCl)Fisher ScientificS27110
imidazoleFisher ScientificO3196500
lysozymeFisher ScientificAAJ6070106
magnesium chloride (MgCl2)Fisher ScientificBP214-500
Pierce Universal NucleaseFisher ScientificPI88700Benzonase (Sigma-Aldrich cat. # E1014) is an acceptable substitute
Model 120 Sonic DismembratorFisher ScientificFB-120other cell lysis methods (e.g. French Press) can also be effective
5 mL HiTrap chelating HP columnGE Life Sciences17040901any nickel-affinity chromatography column or resin could be substituted
nickel(II) sulfate hexahydrateFisher ScientificAC415611000for charging HiTrap column
0.8 µm pore size cellulose acetate syringe filtersFisher Scientific09-302-168
Bradford reagentBio-Rad5000205
Tris bufferFisher ScientificBP1525
Spectrum Spectra/Por 4 RC Dialysis Membrane Tubing 12,000 to 14,000 Dalton MWCOFisher Scientific08-667Bother dialysis membranes with MWCO < 30,000 Da should also work
hydrochloric acid (HCl)Fisher ScientificA144-212for adjusting the pH of Tris-buffered solutions
potassium chloride (KCl)Fisher ScientificP217500
glycerolFisher ScientificBP2294
10x MOPS medium mixtureTeknovaM2101E. coli growth medium
glucoseFisher ScientificD161
monobasic potassium phosphate (KH2PO4)Fisher ScientificBP362-500
dibasic potassium phosphate (K2HPO4)Fisher ScientificBP363-500
dehydrated yeast extractFisher ScientificDF0886-17-0
tryptoneFisher ScientificBP1421-500
magnesium sulfate heptahydrateFisher ScientificM63-50
manganese sulfate monohydrateFisher ScientificM113-500
guanidine isothiocyanateFisher ScientificBP221-250
bovine serum albumin (protease-free)Fisher ScientificBP9703100
clear flat bottom 96-well platesSigma-AldrichM0812-100EAany clear 96-well plate will work
Tecan M1000 Infinite plate readerTecan, Inc.not applicableany plate reader capable of measuring absorbance at 595 and 882 nm will work
ethanolFisher Scientific04-355-451
silica membrane spin columnsEpoch Life Science1910-050/250
ethylenediaminetetraacetic acid (EDTA)Fisher ScientificBP120500
1.5 mL microfuge tubesFisher ScientificNC9580154
ammonium acetateFisher ScientificA637-500
antimony potassium tartrateFisher ScientificAAA1088922
4 N sulfuric acid (H2SO4)Fisher ScientificSA818-500
ammonium heptamolybdateFisher ScientificAAA1376630
ascorbic acidFisher ScientificAC401471000

References

  1. Rao, N. N., Gomez-Garcia, M. R., Kornberg, A. Inorganic polyphosphate: essential for growth and survival. Annual Review of Biochemistry. 78, 605-647 (2009).
  2. Achbergerova, L., Nahalka, J. Polyphosphate--an ancient energy sou....

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