ABSTRACT N°488 - CIGR Section 6 – NANTES – APRIL 2011
Sym'Previus :
Probabilistic approach
to simulate bacterial growth in food
IDEA UNIT PROJECT MANAGER Interactions & dynamics of microbial ecosystems in food Research and Innovation Dpt Créac'h Gwen - F29196 Quimper Cedex - FRANCE Type of presentation. ORAL
Contact person. florence.postollec@adria.tm.fr
Abstract. Sym'Previus is a decision making tool based on predictive microbiology.
Sym'Previus is a collection of tools for food safety inspections designed for food sector businesses to help: Strengthen HACCP plans, Develop new products, Better understand and quantify microbial behaviour, Determine shelf lives and improve food safety. Sym'Previus describes and simulates microbial growth/destruction in food. Sym'Previus models parameters with biological significance. Sym'Previus takes into account batch or intra-species variability in a given food. Keywords. Predictive microbiology, microbial behavior in food, food product shelf-life, food product
safety, decision making tool, microbial growth, new product development
6th INTERNATIONAL CIGR Technical Symposium - Section 6
"Towards a Sustainable Food Chain"
Food Process, Bioprocessing and Food Quality Management
Nantes, France - April 18-20, 2011
ABSTRACT N°385 - CIGR Section 6 – NANTES – APRIL 2011
High pressure treatment of dehydrated products
Colas de la Noue A., PhD student, Pr Perrier-Cornet J-M.*, Pr Gervais P.
Laboratoire de Génie des procédés microbiologique et alimentaire, Université de Bourgogne, 1, esplanade Erasme, 21000 Dijon Type of presentation. ORAL
Contact person. alexandrecolas@gmail.com
Abstract.Decontamination of dried food products is still a challenge. Produced most of the
time in Southern countries, spices are raw products highly exposed to contamination due to their manufacturing conditions. Most of the current decontamination processes go through a hydration phase followed by a drying phase, such as bleaching or steam treatment. These treatments are expensive and energy consuming. Ionization, another well known process, is efficient but raises concerns among consumers. High hydrostatic pressure for mild treatment of liquid products is already used for fruit juices or other hydrated products and attributes high organoleptic properties. Gases under pressure such as carbon dioxide are widely studied, but require most of the time water, very long residence time and heating of the product to kill most resistant forms. Recently, it has been proven that dried microorganisms like yeasts could be inactivated by more than 6 log of destruction by high isostatic gas pressure. The major benefit of this process is the use of inert gases such as nitrogen, which, in theory, does not affect sensitive molecules. Latest experiments show that spores of bacteria and fungi can also be inactivated by this process reaching more than 2 log of inactivation. The efficiency of this treatment seems to be governed by different parameters: nature of the gas, level of pressure, holding time, release kinetic of the gas and level of hydration of the microorganisms. The lower the hydration is, the higher the destruction. The process is separated into three phases: first, the pressure is raised to a certain level (between 150 and 500 MPa), then a maintenance time permits the sorption of the gases, and finally, the gas is quickly released from the matrix (at about 75 MPa.s- 1). This last step is very important for the destruction; if the gas is released slowly, dried microorganisms can support very high levels of pressure without any damage. An avenue to explain the destruction of microorganisms could be in the sorption of the gases in different compartments of the cells followed by the rapid desorption of gases, causing an alteration of the membrane integrity. The above mentioned mechanisms are not yet well understood. The study of the effects of these treatments on macromolecules could offer additional explanations, and permit the development of new athermal decontamination technologies. Keywords. Bacterial spore, high pressure, gas, inactivation, dried products
*jm.perrier@agrosupdijon.fr -Tel. : 33 (0)3 80 77 40 04 -Fax : 33 (0)3 80 39 68 98
6th INTERNATIONAL CIGR Technical Symposium - Section 6
"Towards a Sustainable Food Chain"
Food Process, Bioprocessing and Food Quality Management
Nantes, France - April 18-20, 2011
ABSTRACT N°291 - CIGR Section 6 – NANTES – APRIL 2011
Evaluation of the role of water content on bacterial
spores heat inactivation
Julia Hauck Tiburski1; Amauri Rosenthal2; Jean-Marie Perrier-Cornet1; Dominique
Champion3; Patrick Gervais1*;
1 Laboratoire de Génie des Procédés Microbiologiques et Alimentaires (GPMA), Université de Bourgogne/AgroSup Dijon, 1 Esplanade Erasme, 21000, Dijon, France; +3-380774004; fax: +33-380772385; 2 EMBRAPA LABEX Europe. Hosting Institution : GPMA Université de Bourgogne/Agrosup Dijon 3 Equipe "Eau—Molécules actives—Macromolécules—Activités"; Université de Bourgogne/Agrosup Dijon Type of presentation. ORAL
Contact person. Patrick Gervais (gervais@u-bourgogne.fr)

Bacterial spores are formed when conditions for growth are unfavorable. Spores are
metabolically dormant and resistant to a wide range of environmental conditions including wet and
dry heat, UV and gamma radiation, extreme desiccation, and oxidizing agents. Multiple factors are
involved in spore resistance properties, most related to the structure of the spore including the
relative dehydration of spore core. The purpose of this study was to investigate the role of the water
content of Bacillus subtilis spores in their heat inactivation.
Bacillus subtilis spores were equilibrated at different water activities (aw 0.1 to 0.5) and Differential
Scanning Calorimetry
(DSC) was used to simulate a heat treatment under controlled conditions of
linearly increasing temperature (25 to 220°C). Aluminium pans with different pressure resistances
(0.1 and 0.5 MPa) were used in order to allow water to evaporate at different temperatures. After the
treatment, spore viability was assessed by plate count. The thermally induced transitions were
determined and the relationship between the evaporation of water and cell death was evaluated.

It was observed that even spores with the lowest water activities presented at least one peak related to water evaporation in the thermogram. This result demonstrates that there is water present in the spore protoplast even when the aw is 0.1. When they were submitted to a second heating the thermogram did not exhibit any peaks. The inactivation, after the first heating, was higher in the most resistant pan, which withstood a pressure build up of 0.5 MPa before the evaporation of water. For both pans, the spores with higher water activity were less resistant to inactivation. Therefore, this study indicates that it is possible to maximize inactivation if the heat treatment is applied before the evaporation of water. Keywords. Bacterial spores, Bacillus subtilis, DSC, water content.
6th INTERNATIONAL CIGR Technical Symposium - Section 6
"Towards a Sustainable Food Chain"
Food Process, Bioprocessing and Food Quality Management
Nantes, France - April 18-20, 2011
Biopreservation, a New Hurdle Technology to Improve
Safety and Quality of Seafood Products
Brillet-Viel A.(1,3)*, Pilet M.F (1,2,3), Chevalier F. (2), Cardinal M. (2), Cornet J. (2),
Dousset X. (1,3), Joffraud J.J. (2) & Leroi F. (2)
(1) LUNAM Université, ONIRIS – UMR1014 Sécurité des Aliments et Microbiologie (SECALIM) – Site de la Géraudière - BP 82225 - 44322 Nantes Cedex 3 – France (2) IFREMER – Laboratoire de Science et Technologie de la Biomasse Marine (STBM) - BP 21105 - 44311 Nantes Cedex 03 – France (3) INRA, 44307 Nantes – France * phone : +33251785510, fax : +33251785520 , E-mail : anne.brillet@oniris-nantes.fr Written for presentation at the
2011 CIGR Section VI International Symposium on
Towards a Sustainable Food Chain
Food Process, Bioprocessing and Food Quality Management
Nantes, France - April 18-20, 2011
Abstract. The biopreservation technology consists in preventing growth of unwanted
microorganisms in food by using added selected protective microflora. Three lactic acid bacteria
strains selected for their inhibition properties and their ability to grow at low storage temperatures
have been added in raw salmon fillets and cooked peeled shrimp packed under modified
atmosphere, in comparison with a commercial bacterial strain. For each product, microbiological
analyses and sensory evaluations were performed during the chilled storage to determine the effect
of the protective flora to prevent the spoilage activities. Leuconostoc gelidum EU2247 and
Lactococcus piscium EU2229 allowed to improve the sensory shelf-life of raw salmon and cooked
shrimp respectively by comparison to the non-inoculated control, without any adverse effects
suggesting that biopreservation technology is promising for such applications.
Keywords. Lactic acid bacteria, salmon, shrimp, inhibition, spoilage, sensory analysis, modified
atmosphere packaging.
Proceedings of the 6th CIGR Section VI International Symposium
"Towards a Sustainable Food Chain"
Food Process, Bioprocessing and Food Quality Management
Nantes, France - April 18-20, 2011
Lightly preserved seafood products like fresh fish fillets packed under modified atmosphere, cold smoked fish, carpaccios or cooked shrimp are very sensitive to the growth of pathogenic and spoiling bacteria, due to their physico-chemical characteristics. To improve their shelf-life, chemical preservatives and modified atmosphere packaging (MAP) or a combination of these techniques are generally applied to seafood products. However the growth of undesirable microflora is not always totally prevented and the interest for alternative mild technology such as biopreservation has increased in the last years. This technology consists in adding in food a selected protective microflora for which the inhibition properties have been demonstrated towards pathogenic and/or spoilage bacteria without changing the organoleptic characteristics of the products. Lactic acid bacteria (LAB) have been widely studied for these applications in fermented products. Those last decades, presence of LAB in lightly preserved seafood has been highlighted and selection of protective cultures has intensified. However, an application in seafood still remains a challenge as the LAB must have the capacity to grow in fish matrix poor in carbohydrate, at low temperature and should not change the delicate flavour of marine products. In a previous study, the use of Carnobacterium divergens V41, a bacteriocin-producing strain, allowed keeping the level of Listeria monocytogenes below 50 CFU/g in cold-smoked salmon during 28 days of vacuum storage at 4 and 8°C (Brillet, Pilet, Prévost, Bouttefroy, & Leroi, 2004). Others studies showed that in the presence of the bacteriocinogenic strains C. maltaromaticum CS526 (Yamazaki, Suzuky, Kawai, Inoue, & Montville, 2003) or C. divergens M35 (Tahiri, Desbiens, Kheadr, Lacroix, & Fliss, 2009), the population of L. monocytogenes in cold-smoked salmon decreased after 1 to 3 weeks at 4°C. Non producing-bacteriocin strains can also be used as protective culture against pathogenic bacteria (Nilsson, Hansen, Garrido, Buchrieser, Glaser, Knochel, et al., 2005; Matamoros et al., 2009a). In this case, the inhibition mechanisms are not always known but could be explained by a nutrient competition or a pH decrease due to the production of lactic acid. The use of the biopreservation technology to prevent spoilage is more complex since many bacterial species, both Gram negative and positive, are involved in the off-odors production (Gram & Dalgaard, 2002). Matamoros, Leroi, Cardinal, Gigout, Kasbi Chadli, Cornet et al. (2009a) have shown the capacities of psychrotrophic strains of Lactococcus piscium and Leuconostoc gelidum to significantly improve the sensory quality of cold-smoked salmon and cooked peeled shrimp however the effect was very variable depending on strains and products. For that reason, it is interesting to select the best strain adapted to each product taking into account the variability of the raw material and to extend the application to other marine products such as raw salmon fillets stored under MAP. In this work, two strains of psychrotrophic Ln. gelidum, one strain of Lc. piscium and one commercial starter LLO have been tested on MAP cooked peeled shrimp and fresh salmon fillets, two increasing products on the European market. Materials and Methods
Bacterial Strains and Cultures Conditions
Ln. gelidum strains (EU2247 and EU2262) and Lc. piscium (EU2229) were isolated from commercial seafood products by Matamoros, Pilet, Gigout, Prévost & Leroi (2009b). The starter LLO is a commercial strain used as a bioprotective agent in seafood products (Biocéane, Nantes, France). The strains were stored at -80°C in their growth medium with 10% (v/v) sterile glycerol. All strains were subcultured for 48h at 15°C and cultured for 18h at 20°C in Elliker broth (Biokar Diagnostics, Beauvais, France). Antibacterial Activity of Leuconostoc gelidum and Lactococcus piscium in
seafood products (challenge tests)

The following products were provided by industrial partners : two batches of commercial fresh salmon fillets (Salmo salar farmed in Norway, portions 140 g) which differ with the processing plant (factories A and B) and the quality of fillets (Red Label and Norway Superior) and two batches of commercial cooked peeled shrimp (Penaeus vannamei, 71/90 size) which differ with the origin of farming place (Colombia and Thailand) and the presence/absence of sulphites additives. Products were freshly processed and inoculated within the following hours. Each batch of product was divided in five sub-batches inoculated with : (1) Ln. gelidum EU2247, (2) Ln. gelidum EU2262, (3) Lc. piscium EU2229, (4) the commercial starter LLO and (5) non-inoculated (control). For this, an appropriate dilution was aseptically sprayed on each side of raw salmon fillets (2% v/w) and cooked peeled shrimp (5% v/w) with a trigger sprayer ("Diamant 0.6L RCM", Nantes, France). The initial desired level of LAB in the flesh was 106 CFU g-1. Immediately after inoculation, the salmon fillets and portions of shrimp (125 g) were packed in punnets under modified atmosphere (50% N2 - 50% CO2; Multivac T252, Wolfertschwenden, Germany) with a product/gas ratio of approximately 2/1. The salmon fillets and portions of shrimp were stored at 2°C (3 days and 7 days respectively) and then at 8°C according to the industrial recommendations until sensory rejection of the products. Microbiological Analysis
Microbiological analyses were performed at day 0 and day of sensory spoilage. Salmon and shrimp samples (50 g taken from 3 punnets) were homogenized and diluted in 200 ml chilled physiological saline containing 0.85% (w/v) NaCl and 0.1% (w/v) tryptone (Biokar Diagnostics) for 2 min in a stomacher (Lab. Blender, London, UK). After 20 min at room temperature, the homogenate was 10-fold serially diluted in physiological saline, and 0.1 ml of each appropriate dilution was spread-plated in duplicate. For inoculated samples, total LAB were enumerated on Elliker or MRS medium. Plates were incubated at 12°C for 5-6 days in anaerobic conditions. For controls, total psychrotrophic counts were enumerated on Long & Hammer medium at 15°C, as described by Cardinal, Gunnlaugsdottir, Bjoernevik, Ouisse, Vallet, & Leroi (2004). Sensory Analysis
After six days of storage, sensory analyses were performed daily on non-inoculated products (controls), the objective being to determine the sensory rejection time of controls. Nine regularly trained people from an internal panel (IFREMER) classified the controls into the following three classes defined by spoilage level on the basis of odor : not spoiled, lightly spoiled, strongly spoiled. Two major odor descriptors were also given by the trained panel. At the sensory rejection time, determined when 50% of the panelists classified controls in the "strong spoilage" level, all the samples of the respective batch inoculated with protective LAB were analyzed by the panel as described for the controls (spoilage level, two odor descriptors). Additionally the panelist scored the global off-odor perception on an unstructured line scale from zero (low intensity) to ten (high intensity). Results and Discussion
Challenge tests in raw salmon fillets
Microbiological and sensory analyses were performed on two batches of raw salmon fillets inoculated with protective cultures during chilled storage (Figure 1). The spoilage of the Red Label control was noted after nine days of storage, and after six days for the Norway Superior control. Figure 1. Sensory analysis of raw salmon fillets at the spoilage day and microbiological analysis: (a) Quality "Red Label", factory A, Norway (Day 9); (b) Quality "Norway Superior", factory B, Norway (Day 6). Note 0 : not spoiled, Note 10 : strongly spoiled. The results presented in Figure 1 show that all the protective cultures were inoculated at the desired level and grew easily in this product reaching 3.108 to 109 CFU g-1. The addition of these protective cultures on raw salmon fillets led to a reduction of off-odors. The best results were obtained with the Red Label samples inoculated with Ln. gelidum EU2247 showing no off-odors (note <1) and characterized by freshness descriptors whereas the control was considered as strongly spoiled (score nearly 8/10) with strong sour and acid off-odors. The commercial starter LLO showed results as good as Ln. gelidum EU2247 with samples scored <1 on the spoilage scale (no significant difference with the Duncan test at the 0.05 level of probability). Additional sensory tests performed after the sensory rejection time of the control (data not shown) indicate that those strains could also increase the shelf-life but more analysis should be required to precisely determine the extension time. In the Norway Superior samples, none of the protective cultures tested was able to prevent efficiently the spoilage although better results were again observed with Ln. gelidum EU2247 and starter LLO (score around 3-4 versus 6 for control). It is important to note that the initial total psychrotrophic microflora level of the control batch was clearly higher than the Red Label, leading to the rapid off-odors detection after processing. As previously described by Brillet, Pilet, Prévost, Cardinal & Leroi (2005), the biopreservation strategy can not improve quality nor safety in products of low hygienic quality but must be considered as an interesting extra hurdle technology in products of high hygienic quality. The better efficacy of Ln. gelidum EU2247 could be explained by the production of a bacteriocin-like component active against Lactobacillus farciminis which is sometime involved in MAP fish spoilage. On the other hand, this compound was not active against other major spoiling microorganisms such as Brochothrix thermosphacta, Shewanella putrefaciens, Pseudomonas sp. and Serratia liquefaciens (Matamoros, Pilet, Gigout, Prévost & Leroi, 2009b) suggesting that other mechanisms may be involved. Challenge tests in cooked peeled shrimp
Results of microbiological and sensory analyses for the two batches of cooked peeled shrimp inoculated with protective cultures are presented in Figure 2. The first batch (a in figure 2) was farmed in Colombia and sulphites were added after slaughtering. The second one (b) was farmed in Thailand and contained no sulphite. The spoilage was recorded at day 13 for the two batches. Figure 2. Sensory analysis of cooked peeled shrimp at the spoilage day (day 13) and microbiological analysis: (a) Colombia, presence of sulphites; (b) Thailand, absence of sulphites. Note 0 : not spoiled, Note 10 : strongly spoiled. All the LAB strains developed well in shrimp although higher counts (approx. 1-2 log CFU g-1) were observed in the batch without sulphites (Figure 2). The four protective cultures significantly improved the sensory quality of the products but in all cases the best results were obtained with Lc. piscium EU2229 : at day 13, the score of the samples inoculated with this strain was below 2 and 1 in batches (a) and (b) respectively and the main odors descriptor were closed to those of fresh products (crustacean, rice). The others strains were less effective to limit the emergence of off-odors. It is noteworthy that Lc. piscium EU2229 grew better in shrimp that the other strains, and this is particularly the case for product with sulphites. Fall, Leroi, Cardinal, Chevalier & Pilet (2010) showed that the improvement of the sensory quality of cooked peeled shrimp by another Lc. piscium strain could be linked to the inhibition of the specific spoiling bacteria B. thermosphacta. Conclusions
The results obtained in this study have demonstrated the efficiency of biopreservation to improve the sensory quality of seafood products during their storage. Ln. gelidum EU2247 and Lc. piscium EU2229 are promising agents for a biopreservation strategy in raw salmon fillets and cooked peeled shrimp respectively and could be proposed, as the LLO starter, as new protective culture for seafood products. This work was a part of the MIPROMER project coordinated by the Pole Agronomique Ouest, and was supported by grants from the regions of Bretagne and Pays de la Loire. References
Brillet, A., Pilet, M.F., Prévost, H., Bouttefroy, A., & Leroi, F. 2004. Biodiversity of Listeria
monocytogenes sensitivity to bacteriocin-producing Carnobacterium strains and
application in sterile cold-smoked salmon. Journal of Applied Bacteriology 97: 1029-
Brillet, A., Pilet, M.F., Prévost, H., Cardinal, M., & Leroi, F. 2005. Effect of inoculation of Carnobacterium divergens V41, a biopreservative strain against Listeria monocytogenes
risk, on the microbiological, chemical and sensory quality of cold-smoked salmon.
International Journal of Food Microbiology 104 : 309-324.
Cardinal, M., Gunnlaugsdottir, H., Bjoernevik, M., Ouisse, A., Vallet, J.L., & Leroi F. 2004. Sensory characteristics of cold-smoked Atlantic salmon (Salmo salar) from European
market and relationships with chemical, physical and microbiological measurements.
Food Research International 37: 181-193.
Fall, P.A., Leroi, F., Cardinal, M., Chevalier, F., & Pilet, M.F. 2010. Inhibition of Brochothrix thermosphacta and sensory improvement of tropical peeled cooked shrimp by
Lactococcus piscium CNCM I-4031. Letters in Applied Microbiology 50: 357-361.
Gram, L. & Dalgaard, P. 2002. Fish spoilage bacteria – problems and solutions. Current Opinion in Biotechnology 13 : 262-266.
Matamoros, S., Leroi, F., Cardinal, M., Gigout, F., Kasbi Chadli, F., Cornet, J., Prevost, F., & Pilet, M.F. 2009a. Psychrotrophic lactic acid bacteria used to improve the safety and
quality of vacuum-packaged cooked and peeled tropical shrimp and cold smoked
salmon. Journal of Food Protection 72: 365-374.
Matamoros, S., Pilet, M.F., Gigout, F., Prévost, H., & Leroi, F. 2009b. Selection and evaluation of seafood-borne psychrotrophic lactic acid bacteria as inhibitors of pathogenic and
spoilage bacteria. Food Microbiology 26: 638-644.
Nilsson, L., Hansen, T.B., Garrido, P., Buchrieser, C., Glaser, P., Knochel, S., Gram, L., & Gravesen, A. 2005. Growth inhibition of Listeria monocytogenes by a non
bacteriocinogenic Carnobacterium piscicola. Journal of Applied Microbiology 98: 172-
Tahiri, I., Desbiens, M., Kheadr, E., Lacroix, C., & Fliss, I. 2009. Comparison of different application strategies of divergicin M35 for inactivation of Listeria monocytogenes in
cold-smoked wild salmon. Food Microbiology 26: 783-793.
Yamazaki, K., Suzuky, M., Kawai, Y., Inoue, N., & Montville, T.J. 2003. Inhibition of Listeria monocytogenes in cold-smoked salmon by Carnobacterium piscicola CS526 isolated
from frozen surimi. Journal of Food Protection 66: 1420-1425.
Construction of RR Gene Mutants of Lactobacillus
paracasei HD 1.7 and the Impact on the Production of
Jing-Ping Ge, Tian You, Xian-Jun Gao, Xiao-Long Zhao, Wen-Xiang Ping*
Key laboratory of Microbiology, College of Life Science, Heilongjiang University, Harbin 150080, P.R.China. Author for correspondence Fax: +86-0451-86609016; Email:
gejingping@126.com. Written for presentation at the
2011 CIGR Section VI International Symposium on
Towards a Sustainable Food Chain
Food Process, Bioprocessing and Food Quality Management
Nantes, France - April 18-20, 2011
Abstract. [Objective] A suicide plasmid pUC18-prcR-tet was constructed to knock out prcR gene in
Lactobacillus paracasei HD1.7, which was imported to Lactobacillus paracasei HD1.7. The knockout
mutant strains of prcR gene were obtained and their situations of antimicrobial were observed.
[Methods] On the basis of plasmid pUC18, two components were integrated, which were prcR gene
from Lactobacillus paracasei HD1.7 and tetracycline resistance gene as tetracycline resistant
marker. After enzyme digestion and ligation, the suicide plasmid pUC18-prcR-tet was constructed. In
this plasmid, both upstream and downstream of tetracycline resistance gene have fragments (about
400 bp) of prcR as a way of homologous recombination. The pUC18-prcR-tet was imported to the
L.paracasei HD1.7 by electrotransformation and the situation of the knockout mutant strains of prcR
gene was observed by antimicrobial test. [Results] The mutant strain of prcR was accessed by the
gene knockout technology. By antimicrobial test, that degree of antimicrobial of mutant strains was
weaker than that of the original strains was discovered, which indicated that genes that affected
antimicrobial peptides were changed, which affected production of antimicrobial peptides.
[Conclusions] The suicide plasmid pUC18-prcR-tet was successfully constructed, which was used
to knock out prcR gene in Lactobacillus paracasei HD1.7. By electrotransformation, the mechanism
of the regulation gene prcR was explored, which affects the Quorum-sensing system. The research
can be a potential basis for the exploration of lactic acid bacteria quorum-sensing system and the
mechanism of related regulation genes of antimicrobial peptide and so on.
Keywords. Quorum-sensing, Lactobacillus paracasei HD1.7, suicide plasmid, the gene knockout
technology, prcR, electrotransformation
Proceedings of the 6th CIGR Section VI International Symposium
"Towards a Sustainable Food Chain"
Food Process, Bioprocessing and Food Quality Management
Nantes, France - April 18-20, 2011
Lactobacillus paracasei HD1.7 was isolated from Chinese sauerkraut juice in 2003. Lactobacillus paracasei HD1.7 was the Gram-positive bacteria and belonged in the low GC group (De Vos, Kleerebezem, & Kuipers, 1997)); the fermentation broth of Lactobacillus paracasei HD1.7 contained a kind of peptide Paracin1.7 that could inhibit the growth of several Gram-positive bacteria, Gram-negative bacteria and yeast (Ge, et al., 2009). The process of production of Paracin1.7 had the characteristics of Quorum-sensing. NAKAYAMA AKKERMANS & De Vos (2003) got a series of genes (including histidine protein kinase gene prcK and response regulator prcR) from L.paracasei E93490, which were defined the putitive quorum-sensing components, and predicted that the signaling molecule of L.paracasei E93490 might have antibacterial activity, but they did not do further research about functions of these genes in Quorum Sensing and whether or not the output of antimicrobial peptides related to Quorum Sensing. Accordingly, the similar condition might be existed in L.paracasei HD1.7. Therefore, it is of great significance for us to study fuctions of these related genes in Quorum Sensing and the process of producing antimicrobial peptides by molecular methods. In this study, to construct the suicide plasmid pUC18-prcR-tet applied to the insertional inactivation-based gene knockout technology, plasmid pUC18 was used as the backbone plasmid, and two components were integrated into the plasmid pUC18, which were prcR gene used for homologous recombination and tetracycline resistance gene as tetracycline resistant marker. The pUC18-prcR-tet was imported to the L.paracasei HD1.7 by electrotransformation and knockout mutant strains of prcR gene were obtained. The growth of colonies on the tetracycline resistant plate indicated that homologous recombination between the suicide plasmid pUC18-prcR-tet and the host cell had accomplished. Antimicrobial test was used to show the effect of deletion of prcR on the output of antimicrobial peptides. That provided the basis for further exploring substantial functions of these related genes in Quorum Sensing of L.paracasei. Materials and Methods
Bacterial strains, growth media, and culture conditions
Bacterial strains used were Lactobacillus paracasei HD1.7, Escherichia coli DH5!, Bacillus subtilis, and Staphyloccocus aureus. Lactobacillus paracasei HD1.7 strains were grown in MRS broth and were incubated at 30°C. Strains of Escherichia coli DH5!, Bacillus subtilis, and Staphyloccocus aureus were grown in Luria-Bertani broth and were incubated at 37°C. Primers were synthesized by Invitrogen. The sequences of the primers were shown in Table. 1. Table 1 Primer sequences, templates and their restriction endonuclease sites Primer sequences (5'"3') endonuclease sites TTAGATTACACATCCACACCG CTGCCAGGTTATGGGAAT ATGACNAAYCAYCARAC TGCCAGGTTATGGGAAT Notes: In the orientation of primers, "+" represents the upstream primer and "-" represents the downstream primer; the underlined part is the sequence of restriction endonuclease site. Construction of the recombinant plasmid pUC18-prcR-tet
Plasmid pUC18-prcR was constructed by inserting a 907 bp EcoR I fragment containing prcR from pGM-T-R into the EcoR I gap of plasmid pUC18. Plasmid pUC18-prcR-tet was constructed by inserting a 1.4 kbp Mun I fragment containing tet from pMD18-T-tet into the Mun I gap of pUC18-prcR. The recombinant plasmid pUC18-prcR-tet was then transformed into E. coli competent cells. The plasmid pUC18-prcR-tet was isolated from E. coli cells and restriction enzymes analysis and PCR identification were used to investigate whether the recombinant plasmid pUC18-prcR-tet met the need of the experimental design. Importing the recombinant plasmid pUC18-prcR-tet into Lactobacillus paracasei
HD1.7 by electrotransformation

2 µl of the recombinant plasmid pUC18-prcR-tet and 40 µl of Lactobacillus paracasei HD1.7 competent cells were mixed together well on the ice. The mixture was transferred into precooling 0.2 cm biorad and then the biorad was put on the ice for 5 min. Then the electroporation generator discharged the electric pulse in the 1.8 kV/cm of field strength. After electric shock, 400 µl of MRS broth was added into the biorad immediately and then the mixture was slightly mixed well. The mixture was transferred into 1.5 ml centrifuge tube and was incubated at 30°C under static condition for 5 h. The culture solution was diluted with 100 times. Then 100 µl of the diluent was coated on MRS screening plates with tetracycline and these plates were incubated at 30°C for 7 h. Screening and PCR identification of the knockout mutant strains of prcR gene
The inoculating loops were used to pick up single colonies on the MRS resistant plates with 5 µg/ml (final concentration) of tetracycline. And these single colonies were continuously passage cultured on the MRS resistant plates of tetracycline for 3 4 times. Then the stability of the knockout mutant strains was observed. At the same time, genomic DNA was isolated from the knockout mutant strains with high stability. PCR was used to identify whether homologous recombination had accomplished, which was based on the theoretical design. Antimicrobial condition of fermentation broth of knockout mutant strains
Cylinder plate method (Shen, Fan & Li, 1999) was applied to antimicrobial tests, in which indicator bacteria were Escherichia coli, Bacillus subtilis, and Staphyloccocus aureus, respectively. PCR amplification of three components of constructing the recombinant plasmid

The results of the sequencing of tet, prcR-1 and prcR-2 were analyzed. The result showed that tet, prcR-1 and prcR-2 were successfully cloned (Fig. 1). Fig. 1 PCR results of tet, prcR-1, prcR-2 M, DNA Marker; Lane 1, PCR product of prcR-1 (1276bp); Lane 2, PCR product of prcR-2 (907bp); Lane 3, PCR product of tet (1.4kbp) PCR identification and restriction enzymes analysis of the recombinant plasmid

The pUC18-prcR-tet was isolated from three Escherichia coli DH5! transformants. For PCR identification of pUC18-prcR-tet, pUC18-prcR-tet and the primers PrcR-2-up and PrcR-2-down were used as template and the primers, respectively. It is the same with pUC18-prcR-tet and the primers Tet-up and Tet-down. The results of agarose gel electrophoresis were shown in Fig. 2. For the first PCR, the result showed that an about 2.3 kbp DNA fragment was amplified. The length of this fragment accorded with the total length of prcR (907 bp) and tet (1.4 kbp) both cloned successfully before. For the second PCR, the result showed that an about 1.4 kbp DNA fragment is amplified. The length of this fragment accorded with the length of tet. For restriction enzymes analysis of pUC18-prcR-tet, pUC18-prcR-tet was digested with BamH I and Cla I respectively to judge the relative direction between prcR and tet in the plasmid. The need of the experimental design was that the reading directions of prcR and tet were opposite in order to prevent the protein produced was not the target protein due to continuously reading of prcR and tet,. According to these results and analysis, the recombinant plasmid pUC18-prcR-tet was constructed successfully. Fig. 2 PCR identification results of the recombinant plasmid pUC18-prcR-tet 1: DNA Marker "-EcoT14 I digest; 2-4: PCR product of No.1-3 strains with Tet-up and Tet-down primers; 5-7: PCR product of No.1-3 strains with prcR-2-up and prcR-2-down primers Screening and PCR identification of the knockout mutant strains of prcR gene
Two single colonies growing well on the MRS resistant plates with 5 µg/ml (final concentration) of tetracycline were selected as knockout mutant strains of prcR that are called GXJ-M-1 and GXJ-M-2, respectively. The original strain Lactobacillus paracasei HD1.7 was used in the negative control experiment. The results of agarose gel electrophoresis were shown in Fig. 3. The results showed that there was no DNA fragment that was amplified in the negative control experiment, but an about 500 bp DNA fragment definitely that was amplified in both GXJ-M-1 and GXJ-M-2. However, the concentration of this amplified products were low. This might be due to that tet of plasmid pUC18-prcR-tet was partly integrated into genomic DNA of L.paracasei HD1.7. Fig. 3 The dectection of knockout mutant strains by PCR M, DNA Marker; Lane 1, PCR result of tet using GXJ-M-1 gDNA as template; Lane 2, PCR result of tet using the original strain gDNA as template; Lane 3, PCR result of tet using GXJ-M-2 gDNA as template Antimicrobial condition of fermentation broth of knockout mutant strains
Antimicrobial results of fermentation broth of knockout mutant strains were shown in Table 2. Table 2 showed that the inhibition degree of mutant strains to Bacillus subtilis was generally the same with that of original strains to Bacillus subtilis; the inhibition degree of mutant strains to Escherichia coli was weaker than that of original strains to Escherichia coli, which showed that the output of antimicrobial peptides produced by mutant strains was less than that of antimicrobial peptides produced by original strains; by comparing the inhibition degree of mutant strains to Staphyloccocus aureus with that of original strains to Staphyloccocus aureus, we could infer that the output of antimicrobial peptides produced by mutant strains was also less than that of antimicrobial peptides produced by original strains. Bacillus subtilis was not sensitive to the variation of the concentration of antimicrobial peptides, because it had the spore and stronger tolerance to inhibitors than Escherichia coli and Staphyloccocus aureus. Table 2 Titer of antimicrobial peptide Titer (AU/ml) ( B.sub) 2013.17 1527.50 1876.55 Titer (AU/ml) ( E.coli) Titer (AU/ml) ( S.aureus) 181.83 Conclusions
Gene knockout vector was the tool of the gene knockout technology. So the effect of its construction was greatly significant. This study chose the plasmid pUC18 as the backbone plasmid, which was the narrow host range plasmid and had one single copy and even no copy in G+ bacteria. Because pUC18 could not autonomously replicate in G+ bacteria, the recombinant plasmid pUC18-prcR-tet was integrated into genomic DNA of L.paracasei HD1.7 and replicated with the genomic DNA of L.paracasei HD1.7, only according to the fact that homologous recombination between prcR in the plasmid pUC18-prcR-tet and genome of L.paracasei HD1.7 had accomplished. After homologous recombination, tet in pUC18-prcR-tet was brought in genomic DNA of L.paracasei HD1.7, which made recombinant strains resistant to tetracycline, and the recombinant strains showed the expected pattern for a double cross-over. The successful construction of the recombinant plasmid pUC18-prcR-tet had some influence on the output of antimicrobial peptides of L.paracasei HD1.7, which provided the basis for further exploring substantial functions of these related genes in Quorum Sensing of L.paracasei HD1.7. This study was supported by High-level talents (innovation team) Projects of Heilongjiang University (Hdtd2010-17), Educational Commission of Heilongjiang Province of China (11551z011), the Special Fund for Scientific and Technological Innovative Talents in Harbin (RC2010XK002028), theNational Natural Science Foundation of China (Grant No. 31070446), and National High Technology Research and Development Program of China (863 Program) (No. 2007AA 100702-6). References
De Vos, W. M., Kleerebezem, M., & Kuipers, O. P. 1997. Expression systems for industrial
Gram-positivebacteria with low guanine and cytosine content. Current Opinion in
8(5): 547-553.
Ge, J.-P., Ping, W.-X., Song, G., Du, C.-M., Ling, H.-Z., Sun, X., & Gao, Y. 2009. Paracin 1.7, a bacteriocin produced by Lactobacillus paracasei HD1.7 isolated from Chinese cabbage
sauerkraut, a traditional Chinese fermented vegetable food. Acta Microbiologica Sinica
49(5): 609-616.
NAKAYAMA, J., AKKERMANS, A. D. L., & De Vos, W. M. 2003. High-throughput PCR Screening of Genes for Three-component Regulatory System Putatively Involved in
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Shen, P., Fan X.-R., & Li, G.-W. 1999. Microbiology Laboratory. 3rd ed. Beijing, P.R.China: Higher Education Press.

Source: http://impascience.eu/CIGR/510_proceedings/021_Session2-5-Microbiology.pdf?PHPSESSID=8dda78545b8fe9ea35ba70bbf329428d


The Sec6兾8 complex in mammalian cells: Characterization of mammalian Sec3,subunit interactions, and expressionof subunits in polarized cellsHugo T. Matern*, Charles Yeaman†, W. James Nelson†, and Richard H. Scheller*‡ *Genentech, Inc., Department of Richard Scheller, 1 DNA Way, South San Francisco, CA 94080-4990; and †Department of Molecular and Cellular Physiology,Stanford University Medical School, Stanford, CA 94305

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Share this: March 2016 Volume 11 Number 1 Now Is the Time… to Register From the Editor for the 2016 BIO Conference The generosity of BIO memberswhen it comes to stepping up andhelping out is one of the mostgratifying things for me here atTBC. When I put out a call forassistance, people respond. Casein point: This month differentorganizations in New York areoffering programs of interest tobiographers that I would like tocover in the April issue. Ourdedicated and intrepid NYCcorrespondent, Dona M unker,would attend all of them if shecould, but logistics make itimpossible. At BIO board member