rapid quantitative detection & speciation of contamination in the urban watershed
DESCRIPTION
Rapid Quantitative Detection & Speciation of Contamination in the Urban Watershed. Continuation of WQ1 669 524 94. N W R I. David C. White, Cory Lytle, Ying Dong Gan, Aaron M. Peacock, Kimberly Salome, Yevette M. Picenco, - PowerPoint PPT PresentationTRANSCRIPT
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Rapid Quantitative Detection & Speciation of Contamination in the Urban Watershed
David C. White, Cory Lytle, Ying Dong Gan, Aaron M. Peacock, Kimberly Salome, Yevette M. Picenco,
Institute for Applied Microbiology, University of Tennessee, Knoxville, TNMicrobial Insights, Inc., Rockford, TN,
-IAM
Continuation of WQ1 669 524 94
Microbial Insights, Inc.
N W R I
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WQ1 669 524 94
Objectives: 1). Rapid (< 1 hr) Quantitative sensitive method for CONTAMINATION*
Detection to monitor multiple sites in the watershed
2). Allows for” regionalized” intensive treatment in an integrated watershed system
CONTAMINATION*
Drugs, hormones & other pharmaceutically active compounds -ppb
Differentiate Pathogenic Bacteria including especially VBNC pathogens ~ Enterics, Legionella, Mycobacteria, indicators for virus
Protozoa Cryptosporidium, Giardia , Microsporidium, Algae
Indicators pf pathogen infectivity
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1. Strategically placed coupons at multiple sites for biofilm formation
2. Biofilms are readily invaded by Pathogens and Nurtured
3. Lipids in biofilms serve as a built in solid phase extractor for hydrophobic drugs, hormones, bioactive agents
5. Convenient to recover & analyze for biomarkers Its not in the water but the slime on the coupon
Sampling Urban Watershed --- Scheme #1
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6. Coupon sequentially extracted high pressure/temperature
Supercritical Carbon Dioxide Neutral Lipids
(residue) Chloroform/methanol Polar lipids Analysis by HPLC/ES/MS/MS
(residue) Mild Acid , SFE Lipopolysaccharide OH FA Analysis by GC/MS
7. Analysis on GIS Basis by automatons neural network ANN
8. Feedback to purification interdiction systems
Sampling Urban Watershed --- Scheme # 2
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1. Add from continuous culture vessels:Pseudomonas Spp.Acetovorax spp.Bacillus spp.
2. Seed with trace surrogate/pathogen E. coli (GFP), Mycobacterium pflei (GFP), Legionella bosmanii , Sphingomonas
In the Drinking Water Biofilm
Reproducibly Generate a Drinking Water Biofilm:
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Biofilm Test System
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Detecting specific pollution: Drugs, hormones bioactive compounds
Recover from biofilms: Triculture biofilm + E. coli (GFP) established 3 days in presence of 1000
ppb drug Extract EI/MS/MS
Beads Beads +Biofilm Waste Caffeine 4.7% 50 ppb 3.7% 37 ppb ~97% Triclosan* 3.7% 37 ppb 15% 160 ppb ~ 84% Monensin** ~ 0 % 0.18 1.8 ppb ~99%Finasterdine*** ~ 0% 0.4 % 4.2 ppb ~98 % Caffeine LOD ~ 2 ppb*disinfectant widely used in toiletries LOD ~25 ppb ***macrolide antibiotic used as antiparastic in cattle & chickens factories
LOD~2 ppb *****(Proscar) inhibitor of testosterone hydroxylase LOD ~ 300 ppt *
Biofilms concentrate bioactives compared to sterile surface
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ESI (cone voltage) Q-1 CAD Q-3
ESI/MS/MS
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+Q1: 0.118 to 0.480 min from Sample 1 (finasterdine) of 0928002.wiff Max. 7.4e6 cps.
200 210 220 230 240 250 260 270 280 290 300 310 320 330 340 350 360 370 380 390 400m/z, amu
0.0
5.0e5
1.0e6
1.5e6
2.0e6
2.5e6
3.0e6
3.5e6
4.0e6
4.5e6
5.0e6
5.5e6
6.0e6
6.5e6
7.0e6
7.4e6
In
te
ns
ity
, c
ps
373.7
374.7
395.6
365.3
397.7366.5202.4 343.4253.5231.2 371.7
+Product (373.7): 119 MCA scans from Sample 2 (finasterdine) of 0928002.wiff Max. 1.6e8 cps.
100 120 140 160 180 200 220 240 260 280 300 320 340 360 380 400m/z, amu
0.0
1.0e7
2.0e7
3.0e7
4.0e7
5.0e7
6.0e7
7.0e7
8.0e7
9.0e7
1.0e8
1.1e8
1.2e8
1.3e8
1.4e8
1.5e8
1.6e8
In
te
ns
ity
, c
ps
373.3
305.4
374.4
317.2175.1121.3 189.3147.4 255.4220.3107.2 161.3 215.4 355.3249.3 272.4
NH
O
CH3
CH3
NH
O
CH3
CH3
H3C
H C23H36N2O2Exact Mass: 372.28
Mol. Wt.: 372.54
Finasterdine Q1 scan
Product ion scan305.4
373.3
373.3
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Coupon + Biofilm Extract with SFECO2
1. Neutral Lipids UQ isoprenologues UQ-8 Enterics, UQ-9 Pseudomonas, UQ-10 Protozoa
Derivatize –N-methyl pyridyl Diglycerides (cell lysis)Sterols, Cholesterol (Protozoa), Ergostrerol (Fungi)
Extract Residue with Chloroform.methanol
2. Polar Lipids
Transesterify, GC/MS . 30H 10:0, 12:0 – Pseudomonas
30H 14:0 -- pathogens & enterics
Lipid Biomarkers
Phospholipids, PC, PE, PG, & sn1 sn2 FAAmino Acid PG, 0rnithine lipids, Plasmalogens
3. LPS OH FA
Acidify, Extract residue with SFECO2
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Q6
Q7Q10
O
O
H3OC
H3OC
CH3
]H
n
197 m/z
Respiratory Ubiquinone (UQ)
LOD = 3 ppb (3.7 fmol/uL) ~ 104 Bacteria , UQ-8 E. coli & Enterics,
UQ-9 Pseudomonas, UQ-10 Protozoa, Algae, UQ-12,13 Legionella
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Parent product ion MS/MS of synthetic PG Q-1 1ppm PG scan m/z 110-990 (M –H) -
Sn1 16:0, Sn2 18:2
Q-3 product ion scan of m/z 747 scanned m/z 110-990 Note 50X > sensitivity
SIM additional 5x > sensitivity ~ 250X
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OOP
OO
OH O HN
O
OHO
OHN O
P O
OH
O
O
OH
OO
OO
O
O
O
OH
C93H174N2O24P22-
Exact Mass: 1765.19
Mol. Wt.: 1766.32
14*14*
Gram-negative Bacteria lipid-extracted residue, hydrolize [1% Acetic acid ], extract = Lipid A
Acid sensitive bond
[to KDO]
E. Coli Lipid A 3 OH 14:0*
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Lipid A from E. coliFatty acids liberated by acid hydrolysis followed by
acid–catalyzed (trans) esterification
14:03OH 14:0
3OH 14:0 TMS
phthalatesiloxane
GC/MS of Methyl esters