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1.
BMC Genomics ; 25(1): 910, 2024 Sep 30.
Article in English | MEDLINE | ID: mdl-39350031

ABSTRACT

INTRODUCTION: Black pepper (Piper nigrum L.) is a non-model spice crop of significant agricultural and biological importance. The 'quick wilt' disease caused by the oomycete Phytophthora capsici is a major threat, leading to substantial crop loss. The molecular mechanisms governing the plant immune responses to this pathogen remain unclear. This study employs RNA sequencing and transcriptome analysis to explore the defense mechanisms of P. nigrum against P. capsici. RESULTS: Two-month-old P. nigrum plantlets were subjected to infection with P. capsici, and leaf samples were collected at 6- and 12-hours post-inoculation. RNA was extracted, sequenced, and the resulting data were processed and assembled. Differential gene expression analysis was conducted to identify genes responding to the infection. Additionally, the study investigated the involvement of Salicylic acid (SA), Jasmonic acid (JA), and Ethylene (ET) signalling pathways. Our transcriptome assembly comprised 64,667 transcripts with 96.7% completeness, providing valuable insights into the P. nigrum transcriptome. Annotation of these transcripts identified functional categories and domains, provided details on molecular processes. Gene expression analysis identified 4,714 transcripts at 6 h post-infection (hpi) and 9,416 at 12 hpi as differentially expressed, revealing dynamic regulation of immune-related genes. Furthermore, the study investigated key genes involved in biosynthesis pathways of Salicylic acid, Jasmonic acid, and Ethylene signalling. Notably, we found differential regulation of critical genes associated with these pathways while comparing data before and after infection, thereby shedding light on their roles in defense mechanism in P. nigrum defense. CONCLUSIONS: This comprehensive transcriptome analysis of P. nigrum response to P. capsici attack provides valuable insights into the plant defense mechanisms. The dynamic regulation of innate immunity and the involvement of key signalling pathways highlight the complexity of the plant-pathogen interaction. This study contributes to our understanding of plant immunity and offers potential strategies for enhancing P. nigrum resistance to this harmful pathogen.


Subject(s)
Gene Expression Regulation, Plant , Phytophthora , Piper nigrum , Plant Diseases , Plant Growth Regulators , Signal Transduction , Phytophthora/pathogenicity , Phytophthora/physiology , Piper nigrum/genetics , Piper nigrum/microbiology , Plant Diseases/microbiology , Plant Diseases/genetics , Signal Transduction/genetics , Plant Growth Regulators/metabolism , Gene Expression Profiling , Transcriptome , Disease Resistance/genetics , Oxylipins/metabolism , Cyclopentanes
2.
Molecules ; 29(17)2024 Sep 03.
Article in English | MEDLINE | ID: mdl-39275027

ABSTRACT

Using sous-vide technology in combination with essential oils offers the potential to extend the preservation of food items while preserving their original quality. This method aligns with the growing consumer demand for safer and healthier food production practices. This study aimed to assess the suitability of minimal processing of game meat and the effectiveness of vacuum packaging in combination with Piper nigrum essential oil (PNEO) treatment to preserve red deer meat samples inoculated with Listeria monocytogenes. Microbial analyses, including total viable count (TVC) for 48 h at 30 °C, coliform bacteria (CB) for 24 h at 37 °C, and L. monocytogenes count for 24 h at 37 °C, were conducted. The cooking temperature of the sous-vide was from 50 to 65 °C and the cooking time from 5 to 20 min. Additionally, the study monitored the representation of microorganism species identified through mass spectrometry. The microbiological quality of red deer meat processed using the sous-vide method was monitored over 14 days of storage at 4 °C. The results indicated that the TVC, CB, and L. monocytogenes counts decreased with the temperature and processing time of the sous-vide method. The lowest counts of individual microorganism groups were observed in samples treated with 1% PNEO. The analysis revealed that PNEO, in combination with the sous-vide method, effectively reduced L. monocytogenes counts and extended the shelf life of red deer meat. Kocuria salsicia, Pseudomonas taetrolens, and Pseudomonas fragi were the most frequently isolated microorganism species during the 14-day period of red deer meat storage prepared using the sous-vide method.


Subject(s)
Listeria monocytogenes , Oils, Volatile , Piper nigrum , Listeria monocytogenes/drug effects , Listeria monocytogenes/growth & development , Oils, Volatile/pharmacology , Oils, Volatile/chemistry , Piper nigrum/chemistry , Piper nigrum/microbiology , Animals , Deer/microbiology , Food Preservation/methods , Food Microbiology , Food Storage/methods , Food Packaging/methods , Red Meat/microbiology , Cooking , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/chemistry
3.
World J Microbiol Biotechnol ; 40(11): 330, 2024 Oct 03.
Article in English | MEDLINE | ID: mdl-39358481

ABSTRACT

Trichoderma spp. is primarily applied to manage biotic stresses in plants. Still, they also can mitigate abiotic stresses by the stimulation of antioxidative protective mechanisms and enhanced synthesis of secondary metabolites. The study optimized the conditions to enhance peptaibol production by novel Trichoderma spp, characterized and quantified peptaibol- alamethicin using HPLC and LC MS-MS. The present study investigated these isolates efficacy in enhancing growth and the associated physio-biochemical changes in black pepper plants under moisture stress. Under in vitro conditions, out of 51 isolates studied, six isolates viz., T. asperellum (IISR NAIMCC 0049), T. erinaceum (IISR APT1), T. harzianum (IISR APT2), T. harzianum (IISR KL3), T. lixii (IISR KA15) and T. asperellum (IISR TN3) showed tolerance to low moisture levels (5, 10 and 20%) and higher temperatures (35 and 40 °C). In vivo evaluation on black pepper plants maintained under four different moisture levels (Field capacity [FC]; 75%, 50%, and 25%) showed that the plants inoculated with Trichoderma accumulated greater quantities of secondary metabolites viz., proline, phenols, MDA and soluble proteins at low moisture levels (50% and 25% FC). In the present study, plants inoculated with T. asperellum and T. harzianum showed significantly increased growth compared to uninoculated plants. The shortlisted Trichoderma isolates exhibited differences in peptaibol production and indicated that the peptide might be the key factor for their efficiency as biocontrol agents. The present study also demonstrated that Trichoderma isolates T. harzianum and T. asperellum (IISR APT2 & NAIMCC 0049) enhanced the drought-tolerant capabilities of black pepper by improving plant growth and secondary metabolite production.


Subject(s)
Peptaibols , Piper nigrum , Stress, Physiological , Trichoderma , Piper nigrum/microbiology , Peptaibols/metabolism , Trichoderma/physiology , Trichoderma/metabolism , Tandem Mass Spectrometry , Chromatography, High Pressure Liquid , Alamethicin/metabolism , Alamethicin/pharmacology , Temperature , Secondary Metabolism
4.
Arch Microbiol ; 203(5): 2597-2604, 2021 Jul.
Article in English | MEDLINE | ID: mdl-33693985

ABSTRACT

Yellowing and wilting of black pepper vines is a serious concern in many black pepper growing tracts where Pythium deliense was recently emerged as a pathogen from the rhizosphere of affected vines, which is proved to be pathogenic by Koch's postulates. As a measure to manage the symptoms, bioagents were evaluated against infection by P. deliense. Among the seven bioagents tested, Trichoderma harzianum and Streptomyces albulus showed 100% inhibition in vitro followed by one Streptomyces sp. and S. rimosus (75.33%). The potential ones were further evaluated under the hydroponic system in vivo by challenge inoculation. No root infection was noticed with T. harzianum and S. albulus inoculation, instead, the inoculated plants showed root regeneration. This suggests the efficiency of these bioagents on plant growth promotion as well as on disease suppression. Biochemical analysis of the hydroponic medium showed an increase in membrane conductivity in all the treatments except in T. harzianum. The release of phenolic compounds into the medium was lowest with T. harzianum indicating the prevention of pathogen invasion. In planta evaluation under greenhouse condition and field evaluation also showed the protective effect of T. harzianum and S. albulus with a reduction in the intensity of yellowing to an extent of 73.1% and 71.2%, respectively. The study revealed that T. harzianum and the actinomycete S. albulus had the potential to prevent the root rot caused by P. deliense.


Subject(s)
Biological Control Agents , Hypocreales/physiology , Piper nigrum/microbiology , Plant Diseases , Pythium/physiology , Streptomyces/physiology , Plant Roots/microbiology , Pythium/pathogenicity , Rhizosphere
5.
Food Microbiol ; 98: 103782, 2021 Sep.
Article in English | MEDLINE | ID: mdl-33875210

ABSTRACT

Electrons with energies of 300 keV or lower have the potential to decontaminate the surfaces of various types of food products with minimal loss of quality. The aim of the present work was to determine the thickness of the layer inhabited by microorganisms. The food samples tested were black and white pepper irradiated with 200 keV, 230 keV, 300 keV and 9 MeV beams of electron energy. To determine the depth from the surface which can be inhabited by microorganisms two approaches were tested. The methods used were based on the application of different microbiological recovery techniques and the microbial effectiveness of the irradiation process depending on the energy of the electron beam. It was observed that the layer which microorganisms may contaminate differed for the tested samples it was estimated as being below 100 µm thick for white pepper and about 200 µm for black pepper. The penetration ability was significant in experiments performed, and as a result the electron beam at the lowest levels tested (200 and 230 keV) was found to be insufficient to effectively decontaminate the black pepper samples. The beam of energy 300 keV was found to have a similar microbial inactivation effect as the high energy electron beam (9 MeV).


Subject(s)
Bacteria/radiation effects , Food Contamination/prevention & control , Food Irradiation/methods , Piper nigrum/microbiology , Bacteria/growth & development , Bacteria/isolation & purification , Electrons , Food Contamination/analysis , Food Irradiation/instrumentation , Microbial Viability/radiation effects , Piper nigrum/radiation effects , Vegetables/microbiology , Vegetables/radiation effects
6.
Food Microbiol ; 92: 103575, 2020 Dec.
Article in English | MEDLINE | ID: mdl-32950159

ABSTRACT

Quasimetagenomics refers to the sequencing of a modified food microbiome to facilitate combined detection and subtyping of targeted pathogens in a single workflow. Through quasimetagenomic sequencing, pathogens are detected and subtyped in a shortened time frame compared to traditional culture enrichment and whole genome sequencing-based analyses. While this method was previously used to detect and subtype Salmonella enterica from chicken, iceberg lettuce, and black pepper, it has not been applied to investigate multiple pathogens in one workflow. A quasimetagenomic method to concertedly detect and subtype Salmonella enterica and Escherichia coli O157:H7 from artificially contaminated romaine lettuce in a single workflow was developed. All quasimetagenomic samples with initial target pathogen inoculum levels of ~1 CFU/g were detected and serotyped after co-enrichment of the two pathogens for 12 h. Single nucleotide polymorphism typing was achievable for some initial pathogen inoculum levels as low as ~0.1 CFU/g. Our results suggest that this method can be used for concerted detection and subtyping of multiple bacterial pathogens from romaine lettuce even at low contamination levels.


Subject(s)
Bacterial Typing Techniques/methods , Escherichia coli O157/genetics , Lactuca/microbiology , Metagenomics/methods , Salmonella enterica/genetics , Animals , Chickens , Colony Count, Microbial , Escherichia coli O157/classification , Escherichia coli O157/growth & development , Escherichia coli O157/isolation & purification , Food Contamination/analysis , Genome, Bacterial , Piper nigrum/microbiology , Polymorphism, Single Nucleotide , Salmonella enterica/classification , Salmonella enterica/growth & development , Salmonella enterica/isolation & purification
7.
Food Microbiol ; 92: 103576, 2020 Dec.
Article in English | MEDLINE | ID: mdl-32950160

ABSTRACT

Gaseous treatments with ClO2 and O3 on low-moisture foods (LMFs) have been reported for their efficient bacterial reduction without affecting the external quality of food. However, these studies were conducted on a small scale, which limits their application to LMF industries. We aimed to evaluate the effectiveness of gaseous antimicrobial intervention with ClO2 or O3 to reduce foodborne pathogens (Shiga toxin-producing Escherichia coli, serovars of Salmonella enterica, and Listeria monocytogenes) inoculated on almonds and peppercorns maintained under various conditions. Almonds were treated for over 4 or 6 h. Peppercorns were treated for over 2.5 or 4 h. Gaseous O3 treatment was used for 6 h on almonds and 2 or 4 h on peppercorns. Additionally, the effects of relative humidity (RH) during the treatment of peppercorns and post-treatment heating on almonds were evaluated. Heating at 65 °C post-ClO2 treatment yielded the highest bacterial log reduction of 4.6 CFU/g on almonds, while 80% RH resulted in 3.7-log bacterial reduction on peppercorns. Gaseous O3 resulted in maximum log reductions of 1.3 and 2.5 CFU/g on almonds and peppercorns, respectively. No visual damage was observed. In conclusion, ClO2 was more efficient than O3 and the treatment can be incorporated into industrial practices.


Subject(s)
Chlorine Compounds/pharmacology , Food Preservation/methods , Food Preservatives/pharmacology , Oxides/pharmacology , Ozone/pharmacology , Piper nigrum/microbiology , Prunus dulcis/microbiology , Chlorine Compounds/chemistry , Food Microbiology , Food Preservation/instrumentation , Food Preservatives/chemistry , Gases/chemistry , Gases/pharmacology , Listeria monocytogenes/drug effects , Listeria monocytogenes/growth & development , Oxides/chemistry , Ozone/chemistry , Salmonella enterica/drug effects , Salmonella enterica/growth & development , Seeds/microbiology
8.
J Basic Microbiol ; 60(2): 126-135, 2020 Feb.
Article in English | MEDLINE | ID: mdl-31840846

ABSTRACT

Trichoderma species are recognized as biocontrol agents with great potential in inhibiting fungal pathogens that cause significant crop losses. In this study, 15 Trichoderma isolates were collected from various Egyptian locations. Internal transcribed spacer sequencing revealed four different Trichoderma species; Trichoderma harzianum, Trichoderma asperellum, Trichoderma longibrachiatum, and Trichoderma viride. The antagonistic activity of Trichoderma isolates against Fusarium oxysporum f. sp. capsici was evaluated in vitro. The effect of Trichoderma isolates on pepper growth plants in the presence of F. oxysporum was studied in planta. The inhibition of pathogen mycelial growth in vitro ranged between 35.71% and 85.75%. The isolates Ta3 and Tl had the highest antagonistic ability in vitro against F. oxysporum f. sp. capsici. However, Th7 and Th6 of T. harzianum isolates showed the highest values of disease severity reduction under greenhouse conditions. The genetic diversity of the Trichoderma isolates (Ta1, Ta2, Th1, Th2, Th3, Th4, Th5, and Tv) was investigated on the basis of ISSR and SCoT markers. SCoT primers generated a total of 28 bands, out of which 14 (50%) were polymorphic. ISSR primers gave 32 bands, and 11 of these bands (34.37%) were polymorphic.


Subject(s)
Antibiosis , Fusarium/pathogenicity , Genetic Variation , Pest Control, Biological , Piper nigrum/microbiology , Plant Diseases/prevention & control , Trichoderma/genetics , DNA, Intergenic/genetics , Egypt , Phylogeny , Piper nigrum/growth & development , Plant Diseases/microbiology , Soil Microbiology , Trichoderma/physiology
9.
Food Microbiol ; 82: 388-397, 2019 Sep.
Article in English | MEDLINE | ID: mdl-31027798

ABSTRACT

Salmonella persistence in ground black pepper has caused several foodborne outbreaks and created public concern about the safety of low water activity (aw) foods. In this study, radiofrequency (RF) processing was evaluated for pasteurization of ground black pepper. Stability and homogeneity tests were done for both Salmonella spp. and E. faecium during moisture equilibration before RF heating to evaluate the inoculation method. Moisture content of samples were conditioned such that the final moisture content after RF heating reached the optimal storage moisture. RF heating was shown to provide more than 5.98 log CFU/g reduction for Salmonella spp. and the reduction of 3.89 log CFU/g for E. faecium with a 130 s of treatment time. The higher thermal resistance of E. faecium indicated its suitability as surrogate for Salmonella spp. during RF heating of ground black pepper. Piperine, total phenolics, volatile compounds, and antioxidant activity were assessed as quality parameters for ground black pepper. The results demonstrated that the RF processing provided effective inactivation of Salmonella spp. with insignificant (p > 0.05) quality deterioration.


Subject(s)
Enterococcus faecium/growth & development , Food Microbiology , Heating/methods , Pasteurization/methods , Piper nigrum/microbiology , Salmonella/growth & development , Colony Count, Microbial , Enterococcus faecium/physiology , Food Quality , Hot Temperature , Piper nigrum/chemistry , Salmonella/physiology , Spices/microbiology , Water/analysis
10.
Appl Environ Microbiol ; 84(4)2018 02 15.
Article in English | MEDLINE | ID: mdl-29196295

ABSTRACT

Metagenomics analysis of food samples promises isolation-independent detection and subtyping of foodborne bacterial pathogens in a single workflow. The selective concentration of Salmonella genomic DNA by immunomagnetic separation (IMS) and multiple displacement amplification (MDA) shortened the time for culture enrichment of Salmonella-spiked raw chicken breast samples by over 12 h while permitting serotyping and high-fidelity single nucleotide polymorphism (SNP) typing of the pathogen using short shotgun sequencing reads. The herein-termed quasimetagenomics approach was evaluated on Salmonella-spiked lettuce and black peppercorn samples as well as retail chicken parts naturally contaminated with different serotypes of Salmonella Culture enrichment of between 8 and 24 h was required for detecting and subtyping naturally occurring Salmonella from unspiked chicken parts compared with 4- to 12-h culture enrichment when Salmonella-spiked food samples were analyzed, indicating the likely need for longer culture enrichment to revive low levels of stressed or injured Salmonella cells in food. A further acceleration of the workflow was achieved by real-time nanopore sequencing. After 1.5 h of analysis on a potable sequencer, sufficient data were generated from sequencing the IMS-MDA products of a cultured-enriched lettuce sample to enable serotyping and robust phylogenetic placement of the inoculated isolate.IMPORTANCE Both culture enrichment and next-generation sequencing remain time-consuming processes for food testing, whereas rapid methods for pathogen detection are widely available. Our study demonstrated a substantial acceleration of these processes by the use of immunomagnetic separation (IMS) with multiple displacement amplification (MDA) and real-time nanopore sequencing. In one example, the combined use of the two methods delivered a less than 24-h turnaround time from the collection of a Salmonella-contaminated lettuce sample to the phylogenetic identification of the pathogen. An improved efficiency such as this is important for further expanding the use of whole-genome and metagenomics sequencing in the microbial analysis of food. Our results suggest the potential of the quasimetagenomics approach in areas where rapid detection and subtyping of foodborne pathogens are important, such as for foodborne outbreak response and the precision tracking and monitoring of foodborne pathogens in production environments and supply chains.


Subject(s)
Food Microbiology , Lactuca/microbiology , Meat/microbiology , Piper nigrum/microbiology , Salmonella enterica/isolation & purification , Animals , Chickens , Metagenomics , Nanopores , Sequence Analysis, DNA , Serogroup
11.
Curr Microbiol ; 74(6): 739-746, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28378160

ABSTRACT

White pepper (Piper nigrum L.), a well-known spice, is the main pepper processing product in Hainan province, China. The solid-state method of fermentation can peel pepper in a highly efficient manner and yield high-quality white pepper. In the present study, we used next-generation sequencing to reveal the dynamic changes in the microbiota during pepper peeling by solid-state fermentation. The results suggested that the inoculated Aspergillus niger was dominant throughout the fermentation stage, with its strains constituting more than 95% of the fungi present; thus, the fungal community structure was relatively stable. The bacterial community structure fluctuated across different fermentation periods; among the bacteria present, Pseudomonas, Tatumella, Pantoea, Acinetobacter, Lactococcus, and Enterobacter accounted for more than 95% of all bacteria. Based on the correlations among the microbial community, we found that Pseudomonas and Acinetobacter were significantly positively related with A. niger, which showed strong synergy with them. In view of the microbial functional gene analysis, we found that these three bacteria and fungi were closely related to the production of pectin esterase (COG4677) and acetyl xylan esterase (COG3458), the key enzymes for pepper peeling. The present research clarifies the solid-state fermentation method of pepper peeling and lays a theoretical foundation to promote the development of the pepper peeling process and the production of high-quality white pepper.


Subject(s)
Acinetobacter/genetics , Aspergillus niger/genetics , Fermentation/physiology , Microbiota/genetics , Piper nigrum/microbiology , Pseudomonas/genetics , Vegetables/microbiology , Acetylesterase/metabolism , Acinetobacter/classification , Acinetobacter/isolation & purification , Aspergillus niger/classification , Aspergillus niger/isolation & purification , Carboxylic Ester Hydrolases/metabolism , China , Food Handling/methods , High-Throughput Nucleotide Sequencing , Pseudomonas/classification , Pseudomonas/isolation & purification
12.
Int J Mol Sci ; 18(12)2017 Dec 07.
Article in English | MEDLINE | ID: mdl-29215548

ABSTRACT

Bragantina and Cingapura are the main black pepper (Piper nigrum L.) cultivars and the Pará state is the largest producer in Brazil with about 90% of national production, representing the third largest production in the world. The infection of Fusarium solani f. sp. piperis, the causal agent of Fusarium disease in black pepper, was monitored on the cultivars Bragantina (susceptible) and Cingapura (tolerant), during 45 days' post infection (dpi). Gas Chromatography-Mass spectrometry (GC-MS) analysis of the volatile concentrates of both cultivars showed that the Bragantina responded with the production of higher contents of α-bisabolol at 21 dpi and a decrease of elemol, mostly at 30 dpi; while Cingapura displayed an decrease of δ-elemene production, except at 15 dpi. The phenolic content determined by the Folin Ciocalteu method showed an increase in the leaves of plants inoculated at 7 dpi (Bragantina) and 7-15 dpi (Cingapura); in the roots, the infection caused a phenolic content decrease in Bragantina cultivar at 45 dpi and an increase in the Cingapura cultivar at 15, 30 and 45 dpi. High Performance Liquid Chromatography-Mass spectrometry (HPLC-MS) analysis of the root extracts showed a qualitative variation of alkamides during infection. The results indicated that there is a possible relationship between secondary metabolites and tolerance against phytopathogens.


Subject(s)
Disease Resistance , Metabolome , Piper nigrum/metabolism , Fusarium/pathogenicity , Monocyclic Sesquiterpenes , Oils, Volatile/metabolism , Piper nigrum/genetics , Piper nigrum/microbiology , Plant Leaves/metabolism , Plant Leaves/microbiology , Sesquiterpenes/metabolism
13.
J Appl Microbiol ; 120(5): 1219-28, 2016 May.
Article in English | MEDLINE | ID: mdl-26808253

ABSTRACT

AIMS: The objective of this study was to explore antifungal metabolites targeting fungal cell envelope and to evaluate the control efficacy against anthracnose development in pepper plants. METHODS AND RESULTS: A natural product library comprising 3000 microbial culture extracts was screened via an adenylate kinase (AK)-based cell lysis assay to detect antifungal metabolites targeting the cell envelope of plant-pathogenic fungi. The culture extract of Streptomyces mauvecolor strain BU16 displayed potent AK-releasing activity. Rimocidin and a new rimocidin derivative, BU16, were identified from the extract as active constituents. BU16 is a tetraene macrolide containing a six-membered hemiketal ring with an ethyl group side chain instead of the propyl group in rimocidin. Rimocidin and BU16 showed broad-spectrum antifungal activity against various plant-pathogenic fungi and demonstrated potent control efficacy against anthracnose development in pepper plants. CONCLUSIONS: Antifungal metabolites produced by S. mauvecolor strain BU16 were identified to be rimocidin and BU16. The compounds displayed potent control efficacy against pepper anthracnose. SIGNIFICANCE AND IMPACT OF THE STUDY: Rimocidin and BU16 would be active ingredients of disease control agents disrupting cell envelope of plant-pathogenic fungi. The structure and antifungal activity of rimocidin derivative BU16 is first described in this study.


Subject(s)
Colletotrichum/drug effects , Fungicides, Industrial/chemistry , Fungicides, Industrial/pharmacology , Plant Diseases/microbiology , Streptomyces/chemistry , Colletotrichum/growth & development , Molecular Structure , Piper nigrum/microbiology , Plants/microbiology , Polyenes/chemistry , Polyenes/metabolism , Polyenes/pharmacology , Streptomyces/metabolism , Vegetables/microbiology
14.
J Sci Food Agric ; 96(12): 4243-9, 2016 Sep.
Article in English | MEDLINE | ID: mdl-26781479

ABSTRACT

BACKGROUND: Black pepper (Piper nigrum L.) is exposed to microbial contamination which could potentially create public health risk and also rejection of consignments in the export market due to non-adherance to microbial safety standards. The present study investigates the use of microwave (MW) radiation for microbial load reduction in black pepper and analyses the effect on quality. RESULTS: Black pepper was exposed to MWs at two different power levels (663 and 800 W) at an intensity of 40 W g(-1) for different time intervals (1-15 min) and moisture content (110 and 260 g kg(-1) on a wet basis). The exposure of black pepper to MWs at 663 W for 12.5 min was found to be sufficient to reduce the microbial load to the permissible level suggested by the International Commission on Microbiological Specifications for Foods and the European Spice Association. The retention of volatile oil, piperine and resin was 91.3 ± 0.03, 87.6 ± 0.02 and 90.7 ± 0.05%, respectively, in MW-treated black pepper. The final moisture content after MW treatment was found to be 100 ± 1 g kg(-1) for black pepper containing initial moisture of 260 ± 3 g kg(-1) . CONCLUSION: These results suggest that MW heating can be effectively used for microbial load reduction of black pepper without a significant loss in product quality. © 2016 Society of Chemical Industry.


Subject(s)
Bacterial Load/radiation effects , Food Preservation/methods , Fungi/radiation effects , Microwaves , Piper nigrum/microbiology , Piper nigrum/radiation effects , Food Contamination/prevention & control , Food Microbiology/methods , Food Quality , Food Safety/methods , Heating , Microbial Viability/radiation effects , Piper nigrum/chemistry
15.
Food Microbiol ; 52: 185-96, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26338134

ABSTRACT

A liquid chromatography triple quadrupole tandem mass spectrometry method was developed and validated to determine mycotoxins, produced by fungal isolates grown on malt extract agar (MEA). All twenty metabolites produced by different fungal species were extracted using acetonitrile/1% formic acid. The developed method was applied to assess the toxigenic potentiality of Aspergillus flavus (n = 11) and Aspergillus parasiticus (n = 6) strains isolated from black peppers (Piper nigrum L.) following their growth at 22, 30 and 37 °C. Highest mean radial colony growth rates were observed at 30 °C for A. flavus (5.21 ± 0.68 mm/day) and A. parasiticus (4.97 ± 0.33 mm/day). All of the A. flavus isolates produced aflatoxin B1 and O-methyl sterigmatocystin (OMST) while 91% produced aflatoxin B2 (AFB2) and 82% of them produced sterigmatocystin (STERIG) at 30 °C. Except one, all the A. parasiticus isolates produced all the four aflatoxins, STERIG and OMST at 30 °C. Remarkably high AFB1 was produced by some A. flavus isolates at 22 °C (max 16-40 mg/kg). Production of mycotoxins followed a different trend than that of growth rate of both species. Notable correlations were found between different secondary metabolites of both species; R(2) 0.87 between AFB1 and AFB2 production. Occurrence of OMST could be used as a predictor for AFB1 production.


Subject(s)
Aspergillus flavus/isolation & purification , Aspergillus/isolation & purification , Chromatography, High Pressure Liquid/methods , Mycotoxins/chemistry , Piper nigrum/microbiology , Tandem Mass Spectrometry/methods , Aspergillus/chemistry , Aspergillus/genetics , Aspergillus/metabolism , Aspergillus flavus/chemistry , Aspergillus flavus/genetics , Aspergillus flavus/metabolism , Mycotoxins/metabolism
16.
Food Microbiol ; 49: 226-30, 2015 Aug.
Article in English | MEDLINE | ID: mdl-25846935

ABSTRACT

Contamination of spices by pathogenic and/or spoilage bacteria can be deleterious to consumer's health and cause deterioration of foods, and inactivation of such bacteria is necessary for the food industry. The present study examined the effect of gaseous acetic acid treatment in reducing Escherichia coli O157:H7, Salmonella Enteritidis and Bacillus subtilis populations inoculated on fenugreek seeds and black pepper. Treatment with gaseous acetic acid at 0.3 mmol/L, 0.6 mmol/L and 4.7 mmol/L for 1-3 h significantly reduced the populations of E. coli O157:H7 and Salmonella Enteritidis on black pepper and fenugreek seeds at 55 °C (p < 0.05). The gas treatments at 4.7 mmol/L were more effective in inactivating the pathogens than the treatment at 0.3 mmol/L. An approximately 5.0 log reduction was obtained after 3 h of treatment with 4.7 mmol/L acetic acid. No significant reductions in the population of B. subtilis spores inoculated on fenugreek seeds and black pepper were obtained after the gas treatments at 0.3 mmol/L or 0.6 mmol/L (p > 0.05). However, the gas treatment at 4.7 mmol/L significantly reduced B. subtilis spores (p < 0.05), and 4.0 log CFU/g and 3.5 log CFU/g reductions on fenugreek seeds and black pepper, respectively, were obtained after 3 h of treatment.


Subject(s)
Acetic Acid/pharmacology , Disinfectants/pharmacology , Disinfection/methods , Piper nigrum/microbiology , Trigonella/microbiology , Acetic Acid/chemistry , Bacillus subtilis/drug effects , Bacillus subtilis/growth & development , Disinfectants/chemistry , Escherichia coli O157/drug effects , Escherichia coli O157/growth & development , Gases/chemistry , Gases/pharmacology , Salmonella enteritidis/drug effects , Salmonella enteritidis/growth & development , Seeds/microbiology
17.
J Appl Microbiol ; 116(4): 890-902, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24387754

ABSTRACT

AIM: To isolate, fermentatively evaluate and identify black pepper (Piper nigrum L.)-associated bacteria for the microbial decortication of fresh ripened berries and dried black pepper for preparation of off-odour-free white pepper. METHODS AND RESULTS: Among 45 bacterial isolates obtained from black pepper, seven of them were found to decorticate black pepper (>60%) and fresh pepper berries (98-100%) into white pepper within 5 days of immersion in bacterial suspension. The 16S rRNA genes (1500-bp amplicon) of these bacteria were sequenced, and species identity was established by closest match in GenBank. Superior-quality white pepper was obtained with Bacillus subtilis (IISR WP 33, 34, 38), Bacillus licheniformis (IISR WP 43), Acinetobacter baumanii (IISR WP 35), Klebsiella pneumoniae (IISR WP 19) and Microbacterium barkeri (IISR WP25). The bacterial isolates were found to secrete multiple hydrolytic enzymes such as cellulase, pectinase, amylase, protease and xylanase. Bacterial cultures were deposited with International Depository Authority at Microbial Type Culture Collection, India, as patent deposits as prescribed in Budapest Treaty for microbial deposits. The white pepper, thus obtained from bacterial decortication process, was free from off-odour compound, especially skatole. Other biochemical constituents such as oleoresin, piperine and essential oils were found in the acceptable range. The bacterial decortication did not affect inherent constituents of pepper such as essential oil constituents, oleoresin and piperine content. CONCLUSION: One of the most significant findings of the work is identification of specific bacterial species for decortication of fresh berries or black pepper berries into value-added white pepper. SIGNIFICANCE AND IMPACT OF THE STUDY: This work paved way for developing a technological process for microbial decortication of fresh/black pepper for the production of superior-quality white pepper.


Subject(s)
Bacteria/metabolism , Fruit/chemistry , Piper nigrum/chemistry , Alkaloids/analysis , Bacteria/enzymology , Bacteria/isolation & purification , Benzodioxoles/analysis , Fermentation , Fruit/metabolism , Molecular Sequence Data , Odorants , Oils, Volatile/chemistry , Piper nigrum/microbiology , Piperidines/analysis , Plant Extracts/analysis , Polyunsaturated Alkamides/analysis , RNA, Ribosomal, 16S/genetics
18.
J Appl Microbiol ; 117(3): 786-99, 2014 Sep.
Article in English | MEDLINE | ID: mdl-24916921

ABSTRACT

AIMS: The study mainly aimed quantitative analysis of IAA produced by endophytic bacteria under various conditions including the presence of extract from Piper nigrum. Analysis of genetic basis of IAA production was also conducted by studying the presence and diversity of the ipdc gene among the selected isolates. MATERIALS AND METHODS: Five endophytic bacteria isolated previously from P. nigrum were used for the study. The effect of temperature, pH, agitation, tryptophan concentration and plant extract on modulating IAA production of selected isolates was analysed by colorimetric method. Comparative and quantitative analysis of IAA production by colorimetric isolates under optimal culture condition was analysed by HPTLC method. Presence of ipdc gene and thereby biosynthetic basis of IAA production among the selected isolates were studied by PCR-based amplification and subsequent insilico analysis of sequence obtained. CONCLUSIONS: Among the selected bacterial isolates from P. nigrum, isolate PnB 8 (Klebsiella pneumoniae) was found to have the maximum yield of IAA under various conditions optimized and was confirmed by colorimetric, HPLC and HPTLC analysis. Very interestingly, the study showed stimulating effect of phytochemicals from P. nigrum on IAA production by endophytic bacteria isolated from same plant. SIGNIFICANCE AND IMPACT OF THE STUDY: This study is unique because of the selection of endophytes from same source for comparative and quantitative analysis of IAA production under various conditions. Study on stimulatory effect of phytochemicals on bacterial IAA production as explained in the study is a novel approach. Studies on molecular basis of IAA production which was confirmed by sequence analysis of ipdc gene make the study scientifically attractive. Even though microbial production of IAA is well known, current report on detailed optimization, effect of plant extract and molecular confirmation of IAA biosynthesis is comparatively novel in its approach.


Subject(s)
Bacteria/metabolism , Carboxy-Lyases/genetics , Endophytes/metabolism , Indoleacetic Acids/metabolism , Piper nigrum/microbiology , Bacteria/genetics , Bacteria/isolation & purification , Carboxy-Lyases/chemistry , Endophytes/genetics , Endophytes/isolation & purification , Genes, Bacterial , Klebsiella pneumoniae/genetics , Phylogeny , Sequence Alignment , Sequence Analysis, Protein
19.
ScientificWorldJournal ; 2014: 829894, 2014.
Article in English | MEDLINE | ID: mdl-24558336

ABSTRACT

Utilization of biological materials in synthesis of nanoparticles is one of the hottest topics in modern nanoscience and nanotechnology. In the present investigation, the silver nanoparticles were synthesized by using the leaf and stem extract of Piper nigrum. The synthesized nanoparticle was characterized by UV-vis spectroscopy, X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), energy dispersive X-ray analysis (EDAX), and Fourier Transform Infrared Spectroscopy (FTIR). The observation of the peak at 460 nm in the UV-vis spectra for leaf- and stem-synthesized silver nanoparticles reveals the reduction of silver metal ions into silver nanoparticles. Further, XRD analysis has been carried out to confirm the crystalline nature of the synthesized silver nanoparticles. The TEM images show that the leaf- and stem-synthesized silver nanoparticles were within the size of about 7-50 nm and 9-30 nm, respectively. The FTIR analysis was performed to identify the possible functional groups involved in the synthesis of silver nanoparticles. Further, the antibacterial activity of the green-synthesized silver nanoparticles was examined against agricultural plant pathogens. The antibacterial property of silver nanoparticles is a beneficial application in the field of agricultural nanotechnology.


Subject(s)
Metal Nanoparticles/chemistry , Piper nigrum/chemistry , Plant Leaves/chemistry , Plant Stems/chemistry , Silver/chemistry , Anti-Infective Agents/chemistry , Host-Pathogen Interactions , Metal Nanoparticles/ultrastructure , Phenotype , Piper nigrum/microbiology , Plant Diseases/microbiology , Plant Extracts/chemistry , Plant Leaves/microbiology
20.
Molecules ; 19(9): 12925-39, 2014 Aug 25.
Article in English | MEDLINE | ID: mdl-25157463

ABSTRACT

The study involved an examination of the antifungal activity on red peppers of pullulan coating (P) and pullulan coating containing either water-ethanol (P + eEMF) or ethanol extract of meadowsweet flowers (P + eEMF). Pullulan was obtained from a culture of Aureobasidium pullulans B-1 mutant. Both non-inoculated peppers and those artificially inoculated with Rhizopus arrhizus were coated and incubated at 24 °C for 5 days. The intensity of the decay caused by Rhizopus arrhizus in the peppers with P and P + eEMF coatings was nearly 3-fold lower, and in the case of P + weEMF 5-fold lower, than that observed in the control peppers. Additionally, the P + weEMF coating decreased, almost two-fold the severity of pepper decay compared to other samples. The influence of coating of pepper postharvest quality was examined after 30 days of storage at 6 °C and 70%-75% RH. All coatings formed a thin and well-attached additional layer of an intensified gloss. During storage, color, total soluble solid content and weight loss of coated peppers were subject to lower changes in comparison with uncoated ones. The results indicate the possibility of the application of pullulan coatings containing MFEs as an alternative to the chemical fungicides used to combat pepper postharvest diseases.


Subject(s)
Piper nigrum/microbiology , Plant Diseases/microbiology , Rhizopus/drug effects , Food Preservation , Fungicides, Industrial/administration & dosage , Glucans/administration & dosage , Glucans/chemistry , Piper nigrum/drug effects , Piper nigrum/growth & development , Plant Diseases/therapy , Plant Extracts/administration & dosage , Plant Extracts/chemistry , Rhizopus/pathogenicity
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