scholarly journals Shigella and Escherichia coli Strategies for Survival at Low pH

1998 ◽  
Vol 51 (Supplement1) ◽  
pp. S81-S89 ◽  
Author(s):  
Pamela L.C. Small
Keyword(s):  
1994 ◽  
Vol 57 (5) ◽  
pp. 431-435 ◽  
Author(s):  
MOHAMMED I. YAMANI ◽  
BASIM A. AL-DABABSEH

Sixty samples of fresh hoummos (chickpea dip) from 15 restaurants were examined in winter and summer to find out numbers and types of microorganisms present. Five reference samples, produced by the investigators under hygienic conditions, were examined for comparison. The microbial load of commercial hoummos was high, and spherical lactic acid bacteria (LAB) belonging to Lactococcus, Enterococcus and Leuconostoc were the predominant microorganisms. The means of the aerobic plate count (APC) and the counts of LAB and coliforms (1.9 × 108, 1.6 × 108 and 2.9 × 105/g, respectively) in summer samples were significantly higher (p < 0.05) than the averages of the same counts in winter samples (2.7 × 107, 1.6 × 107 and 2.2 × 103/g). The average summer and winter yeast counts were 4.2 × 104 and 1.5 × 104g, respectively. In reference samples of hoummos, APC and LAB counts were < 103/g, while the coliform and yeast counts were < 10/g and 102/g, respectively, indicating lack of hygienic practices during the production of commercial hoummos. Salmonella was not detected in any sample, and Escherichia coli and Staphylococcus aureus counts of all samples were < 10/g. The relatively low pH of hoummos (the average pH of all samples was 5.1) and the rapid growth of LAB, possibly accompanied by production of inhibitory substances, may explain the predominance of these bacteria, and could have contributed to the absence of the pathogens examined.


2011 ◽  
Vol 63 (1) ◽  
pp. 29-35 ◽  
Author(s):  
Gordana Zavisic ◽  
Zeljka Radulovic ◽  
Valentina Vranic ◽  
Jelena Begovic ◽  
L. Topisirovic ◽  
...  

The aim of this study was to investigate the probiotic potential of bacteriocin-producing lactobacilli strain Lactobacillus plantarum G2 isolated from the vaginal mucus of healthy women. The antimicrobial effect of G2 was confirmed in the mixed culture with pathogenic Escherichia coli, Staphylococcus aureus, Salmonella abony and Pseudomonas aeruginosa, while bacteriocine activity was detected against S. aureus and S. abony only. The strain showed an excellent survival rate in low pH and in the presence of bile salts. The percentage of adhered cells of L. plantarum G2 to hexadecane was 63.85?2.0 indicating the intermediate hydrophobicity.


IUBMB Life ◽  
2020 ◽  
Vol 72 (5) ◽  
pp. 915-921 ◽  
Author(s):  
Heghine Gevorgyan ◽  
Armen Trchounian ◽  
Karen Trchounian

2001 ◽  
Vol 64 (8) ◽  
pp. 1145-1150 ◽  
Author(s):  
NAVEEN CHIKTHIMMAH ◽  
RAMASWAMY C. ANANTHESWARAN ◽  
ROBERT F. ROBERTS ◽  
EDWARD W. MILLS ◽  
STEPHEN J. KNABEL

Due to undesirable quality changes, Lebanon bologna is often processed at temperatures that do not exceed 48.8°C (120°F). Therefore, it is important to study parameters that influence the destruction of Escherichia coli O157:H7 in Lebanon bologna. The objective of the present study was to determine the influence of curing salts (NaCl and NaNO2) on the destruction of E. coli O157:H7 during Lebanon bologna processing. Fermentation to pH 4.7 at 37.7°C reduced populations of E. coli O157:H7 by approximately 0.3 log10, either in the presence or absence of curing salts. Subsequent destruction of E. coli O157:H7 during heating of fermented product to 46.1°C was significantly reduced by the presence of 3.5% NaCl and 156 ppm NaNO2, compared to product without curing salts (P < 0.01). The presence of a higher level of NaCl (5%) in Lebanon bologna inhibited the growth of lactic acid bacteria (LAB), which yielded product with higher pH (~5.0) and significantly reduced the destruction of E. coli O157:H7 even further (P < 0.05). Lower concentrations of NaCl (0, 2.5%) yielded Lebanon bologna with higher LAB counts and lower pHs, compared to product with 5% NaCl. When lactic acid was used to adjust pH in product containing different levels of NaCl, it was determined that low pH was directly influencing destruction of E. coli O157:H7, not NaCl concentration.


2007 ◽  
Vol 70 (7) ◽  
pp. 1670-1677 ◽  
Author(s):  
DAVID MARALDO ◽  
RAJ MUTHARASAN

We detected Escherichia coli O157:H7 (EC) at approximately 10 cells per ml in spiked ground beef samples in 10 min using piezoelectric-excited millimeter-size cantilever (PEMC) sensors. The composite PEMC sensors have a sensing area of 2mm2 and are prepared by immobilizing a polyclonal antibody specific to EC on the sensing surface. Ground beef (2.5 g) was spiked with EC at 10 to 10,000 cells per ml in phosphate-buffered saline (PBS). One milliliter of supernatant was removed from the blended samples and used to perform the detection experiments. The total resonant frequency change obtained for the inoculated samples was 138 ± 9, 735 ± 23, 2,603 ± 51, and 7,184 ± 606 Hz, corresponding to EC concentrations of 10, 100, 1,000, and 10,000 cells per ml, respectively. EC was detected in the sample solution within the first 10 min. The responses of the sensor to positive, negative, and buffer controls were 36 ± 6, 27 ± 2, and 2 ± 7 Hz, respectively. Verification of EC attachment was confirmed by low-pH buffer release (PBS-HCl, pH 2.2), microscopy, and second antibody EC binding postdetection. The results indicate that PEMC sensors can reliably detect EC at less than 10 cells per ml in 10 min without sample preparation and with label-free reagents.


1998 ◽  
Vol 64 (4) ◽  
pp. 1566-1568 ◽  
Author(s):  
Cristina Garcia-Graells ◽  
Kristel J. A. Hauben ◽  
Chris W. Michiels

ABSTRACT The potential of high-pressure-resistant mutants ofEscherichia coli to survive high-pressure pasteurization in fruit juices and in low-pH buffers was investigated. Treatments with up to 500 MPa of pressure caused only a limited direct inactivation of the mutants but resulted in an accelerated low-pH inactivation during subsequent storage.


1995 ◽  
Vol 58 (10) ◽  
pp. 1059-1064 ◽  
Author(s):  
JOHN P. ERICKSON ◽  
JOSEPH W. STAMER ◽  
MARANDA HAYES ◽  
DENISE N. MCKENNA ◽  
LESLIE A. VAN ALSTINE

An enterohemorrhaghic Escherichia coli O157:H7 (EHEC) outbreak in 1993 was epidemioiogically linked to commercial real mayonnaise. This study evaluated EHEC contamination risk during commercial mayonnaise and mayonnaise dressing production, and EHEC behavior in low-pH dressings. Two potential contamination sources, pasteurized liquid eggs and wet environmental areas, were surveyed for 4 months in three processing plants. One hundred eighty-eight egg lots and 114 environmental swabs were collected and analyzed for EHEC by enrichment and direct plating methods. All plant samples were EHEC negative. Commercial mayonnaise plants which use pasteurized eggs and employ effective good manufacturing practices (GMP) sanitation programs are unlikely EHEC harborage and contamination sources. Five commercial real-mayonnaise-based and reduced-calorie and/or fat mayonnaise dressings were inoculated with ≥6 log10 colony-forming units (CFU)/g EHEC contamination levels and stored at 25°C. The products contained a wide range of acetic acid, NaCl, and preservative levels, while pH varied from 3.21 to 3.94. Products below pH 3.6 rapidly inactivated EHEC, producing ≥7 log10 CFU/g decreases in ≤1 to ≤3 days. High EHEC lethality was also observed in the pH 3.94, egg white-mayonnaise dressing. Intact packages of commercial mayonnaise and mayonnaise dressings pose negligible EHEC contamination and health hazard risks. As with any food, consumers and food-service workers must use stringent hygienic practices to prevent microbial pathogen contamination during preparation, handling, and storage of mayonnaise-ingredient recipes such as chilled perishable salads and salad bar dressings.


2007 ◽  
Vol 35 (6) ◽  
pp. 1606-1609 ◽  
Author(s):  
P.A. Dalby ◽  
J.P. Aucamp ◽  
R. George ◽  
R.J. Martinez-Torres

TK (transketolase) undergoes inactivation during biocatalytic processes due to oxidation, substrate and product inhibition, reactivity of aldehyde substrates, irreversible inactivation at low pH, and dissociation of cofactors. However, the contribution of protein denaturation to each of these mechanisms is not fully understood. The urea-induced reversible denaturations of the apo- and holo-enzyme forms of the homodimeric Escherichia coli TK have been characterized, along with the reconstitution of holo-TK from the apoenzyme and cofactors. An unusual cofactor-bound yet inactive intermediate occurs on both the reconstitution and holo-TK denaturation pathways. The denaturation pathways of the holo- and apoenzymes converge at a second intermediate consisting of a partially denatured apo-homodimer. Preliminary investigation of the denaturation under oxidizing conditions reveals further complexity in the mechanisms of enzyme deactivation that occur under biocatalytic conditions.


1978 ◽  
Vol 171 (3) ◽  
pp. 639-647 ◽  
Author(s):  
Stephen P. Vincent ◽  
Robert C. Bray

Nitrate reductase was purified from anaerobically grown Escherichia coli K12 by a method based on the Triton X-100 extraction procedure of Clegg[(1976) Biochem. J.153, 533–541], but hydrophobic interaction chromatography was used in the final stage. E.p.r. spectra obtained from the enzyme under a variety of conditions are well resolved and were interpreted with the help of the computer-simulation procedures of Lowe [(1978) Biochem. J.171, 649–651]. Parameters for five molybdenum(V) species from the enzyme are given. The low-pH species (gav. 1.9827) is in pH-dependent equilibrium with the high-pH species (gav. 1.9762), the pK for interconversion of the species being 8.26. Of a variety of anions tested, only nitrate and nitrite formed complexes with the enzyme (in the low-pH form), giving modified molybdenum(V) e.p.r. spectra. These complexes, as well as the low-pH form of the free enzyme, showed interaction of molybdenum with a single exchangeable proton. The fifth molybdenum(V) species, sometimes detected in small amounts, appears not to be due to functional nitrate reductase. After full reduction of the enzyme with dithionite, addition of nitrate caused reoxidation of molybdenum to the quinquivalent state, in a time less than the enzyme turnover. Activity of the enzyme in the pH range 6–10 is controlled by a pK of 8.2. It is suggested that the low-pH signal-giving species is the form of the enzyme involved in the catalytic cycle. Iron–sulphur and other e.p.r. signals from the enzyme are briefly described and the enzymic reaction mechanism is discussed.


2011 ◽  
Vol 90 (4) ◽  
pp. 896-900 ◽  
Author(s):  
M.E. Berrang ◽  
W.R. Windham ◽  
R.J. Meinersmann
Keyword(s):  
Low Ph ◽  

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