Abstract:
The evolution of antibiotic resistant pathogens and slow-paced discovery of antibiotics have led
to the requirement of new antibacterial therapies. Indiscrete and disproportionate use of
antibiotics in livestock and poultry is contributing immensely to the development of antibiotic
resistance in bacterial species associated with food contamination. In the light of exponential
increase in bacterial antibiotic resistance, use of natural products (generally recognised as safe)
in combination therapy can be a potent alternative strategy to restrain foodborne illnesses and
contaminations.
Bacterial strains belonging to the genera such as Vibrio, Salmonella, Escherichia and
Listeria are major pathogens implicated in foodborne and gastrointestinal diseases. These
organisms are a constant threat to mankind, and the spread of antibiotic resistance has
compounded the problems. To strategize a combination for antimicrobial activity, traditionally
used antimicrobial compounds were targeted in this study.
Vitamins, metals and essential oils are well known for their antimicrobial activity, and
have been used as food additives for improvement of metabolism in humans. The pro-oxidant
properties of essential oil linalool and vitamin C in combination with copper (LVC) were
exploited for combating multiple antibiotic resistant Vibrio fluvialis and a common foodborne
pathogen Salmonella typhi, using 3-D checkerboard microdilution assay. Antibacterial
propensity in terms of minimum inhibitory concentration revealed that the triple combination
exerted synergistic effect (Fractional Inhibitory Concentration Index-0.48) as compared to
individual constituents. The bactericidal effect of the triple combination was confirmed by
Live/dead staining assay. Reactive oxygen species (ROS) measurements together with TUNEL
assay and scanning electron microscopy imaging strongly suggested that the increase in ROS
production upon the treatment is the underlying mechanism of enhanced antibacterial potency
of the LVC combination. In addition, hypersensitivity of oxidative stress regulator mutants
(oxyR, katG, ahpC and sodA) towards LVC corroborated the involvement of ROS in cell death.
Furthermore, the LVC combination did not display toxicity to human cell lines as confirmed by
MTT assay and could effectively reduce pathogens in food beverages.
Antimicrobial peptides (AMP) are commonly used GRAS status constituents, utilized in
food preservation and antimicrobial therapies. Similar to the antibiotics, AMPs are challenged
with target modified resistant organisms, which abates the efficacy of the peptides. To address
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the problem, a food grade antimicrobial peptide; pediocin was bioconjugated with silver
nanoparticles (AgNPs), to enhance the activity and antimicrobial spectrum of pediocin.
Pediocin-AgNPs (PdSNPs) showed enhanced antimicrobial activity against foodborne
pathogens; Listeria monocytogenes (13 folds) and V. fluvialis (10 folds) in comparison to
citrate capped AgNPs (CSNPs) and pediocin, separately. The bactericidal effect of PdSNPs was
confirmed by kill-kinetics and Live/ dead staining. Upon treatment with PdSNPs, both the
pathogens displayed depolarised and damaged membrane, increased ROS, lesions in DNA and
rapid permeabilization through outer membrane. It is hypothesised that PdSNPs could kill
bacteria by effectively attaching to the cells, penetrating the membrane, and causing oxidative
damage and leakage of ions. It was further demonstrated that PdSNPs could effectively
eradicate mature Listerial biofilm, thus can contribute immensely in food and food
manufacturing units. In addition, PdSNPs did not display any toxicity to mammalian cells and
RBCs, thus could be effectively used as food preservative and in antimicrobial therapy. Hence,
the present study, opens a new approach for combinatorial antimicrobial therapy with food
grade constituents which may be promoted as effective preservatives and alternatives for
antibiotics.
GRAS status organisms and their bioactive compounds were also examined for their
anticancer properties. One of the most important biotherapeutic proteins employed in leukemia
is asparaginase. Conventionally used asparaginases are derived from pathogenic organisms,
hence, have various side effects and toxicity. Thus, in order to mitigate the problems with
conventional asparaginases, there is a desperate requirement for safer enzymes from benign
sources. In this study, asparaginase (AnsLb) from Lactobacillus brevis NKN55 (a probiotic
origin bacterium) was screened, isolated, cloned and expressed in E. coli BL21-AI followed
by affinity purification. The purified protein was found to be a homodimer of 70 kDa, with
monomeric size of approximately 35 kDa. The enzyme showed optimum activity between pH
7.0–8.5 and temperature 35–45°C, which is suitable for human use. AnsLb exhibited no
inhibition with monovalent and divalent metal ions, which depicts it to be a cofactor
independent protein. The apparent Km, Vmax and Kcat values were 0.833 mM, 4.12 mM/min
and 3.045×10-3 sec-1 respectively. Structural studies using CD spectroscopy confirmed change
in helical structure of the protein upon substrate (L-asparagine) binding. As a part of its
utilisation in humans, antileukemic and acrylamide mitigation studies were performed.
Antileukemic potential of AnsLb was explored using murine myeloid leukemic cells, where
the enzyme displayed effective inhibition of the cancer cells. The IC50 value of AnsLb was
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determined to be 11.6 IU, which is comparable with other isolated asparaginases. AnsLb also
exhibited acrylamide lowering property in fried potatoes, where 15 IU/ml could reduce almost
80% of acrylamide in 5 g of fried potatoes. AnsLb did not show any haemolytic activity, thus
has been proved to be safe for human use. In order to increase the utilization spectrum of the
foodgrade asparaginase AnsLb, a better thermotolerant mutant was generated by site specific
mutagenesis, which displayed an increase of 5°C in melting temperature as observed in CD
spectroscopy. Till date very few reports are available on asparaginases from lactic acid
bacteria, and thus this finding can be a substantial step towards discovering safe, foodgrade
antileukemic bioactive molecules.
Overall, the work concludes utilization of food based bioactive molecules for
inhibition of pathogenic bacteria and development of two food grade antibacterial regimens
and their mode of actions for bacterial inhibition. An anticancer molecule was also screened
and it's applicability for commercial utilization was also explored.