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We describe a simple method for rapid quantification of inorganic polyphosphate in diverse bacteria, including Gram-negative, Gram-positive, and mycobacterial species.
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.
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....
1. Purifying Yeast Exopolyphosphatase (ScPPX)
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
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.......
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).
....Name | Company | Catalog Number | Comments |
E. coli BL21(DE3) | Millipore Sigma | 69450 | |
plasmid pScPPX2 | Addgene | 112877 | available to academic and other non-profit institutions |
LB broth | Fisher Scientific | BP1427-2 | E. coli growth medium |
ampicillin | Fisher Scientific | BP176025 | |
isopropyl β-D-1-thiogalactopyranoside (IPTG) | Gold Biotechnology | I2481C | |
HEPES buffer | Gold Biotechnology | H-400-1 | |
potassium hydroxide (KOH) | Fisher Scientific | P250500 | for adjusting the pH of HEPES-buffered solutions |
sodium chloride (NaCl) | Fisher Scientific | S27110 | |
imidazole | Fisher Scientific | O3196500 | |
lysozyme | Fisher Scientific | AAJ6070106 | |
magnesium chloride (MgCl2) | Fisher Scientific | BP214-500 | |
Pierce Universal Nuclease | Fisher Scientific | PI88700 | Benzonase (Sigma-Aldrich cat. # E1014) is an acceptable substitute |
Model 120 Sonic Dismembrator | Fisher Scientific | FB-120 | other cell lysis methods (e.g. French Press) can also be effective |
5 mL HiTrap chelating HP column | GE Life Sciences | 17040901 | any nickel-affinity chromatography column or resin could be substituted |
nickel(II) sulfate hexahydrate | Fisher Scientific | AC415611000 | for charging HiTrap column |
0.8 µm pore size cellulose acetate syringe filters | Fisher Scientific | 09-302-168 | |
Bradford reagent | Bio-Rad | 5000205 | |
Tris buffer | Fisher Scientific | BP1525 | |
Spectrum Spectra/Por 4 RC Dialysis Membrane Tubing 12,000 to 14,000 Dalton MWCO | Fisher Scientific | 08-667B | other dialysis membranes with MWCO < 30,000 Da should also work |
hydrochloric acid (HCl) | Fisher Scientific | A144-212 | for adjusting the pH of Tris-buffered solutions |
potassium chloride (KCl) | Fisher Scientific | P217500 | |
glycerol | Fisher Scientific | BP2294 | |
10x MOPS medium mixture | Teknova | M2101 | E. coli growth medium |
glucose | Fisher Scientific | D161 | |
monobasic potassium phosphate (KH2PO4) | Fisher Scientific | BP362-500 | |
dibasic potassium phosphate (K2HPO4) | Fisher Scientific | BP363-500 | |
dehydrated yeast extract | Fisher Scientific | DF0886-17-0 | |
tryptone | Fisher Scientific | BP1421-500 | |
magnesium sulfate heptahydrate | Fisher Scientific | M63-50 | |
manganese sulfate monohydrate | Fisher Scientific | M113-500 | |
guanidine isothiocyanate | Fisher Scientific | BP221-250 | |
bovine serum albumin (protease-free) | Fisher Scientific | BP9703100 | |
clear flat bottom 96-well plates | Sigma-Aldrich | M0812-100EA | any clear 96-well plate will work |
Tecan M1000 Infinite plate reader | Tecan, Inc. | not applicable | any plate reader capable of measuring absorbance at 595 and 882 nm will work |
ethanol | Fisher Scientific | 04-355-451 | |
silica membrane spin columns | Epoch Life Science | 1910-050/250 | |
ethylenediaminetetraacetic acid (EDTA) | Fisher Scientific | BP120500 | |
1.5 mL microfuge tubes | Fisher Scientific | NC9580154 | |
ammonium acetate | Fisher Scientific | A637-500 | |
antimony potassium tartrate | Fisher Scientific | AAA1088922 | |
4 N sulfuric acid (H2SO4) | Fisher Scientific | SA818-500 | |
ammonium heptamolybdate | Fisher Scientific | AAA1376630 | |
ascorbic acid | Fisher Scientific | AC401471000 |
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