JP2012111704A - Antibacterial agent composition - Google Patents
Antibacterial agent composition Download PDFInfo
- Publication number
- JP2012111704A JP2012111704A JP2010260981A JP2010260981A JP2012111704A JP 2012111704 A JP2012111704 A JP 2012111704A JP 2010260981 A JP2010260981 A JP 2010260981A JP 2010260981 A JP2010260981 A JP 2010260981A JP 2012111704 A JP2012111704 A JP 2012111704A
- Authority
- JP
- Japan
- Prior art keywords
- chitosan
- acetic acid
- antibacterial
- lauryl sulfate
- acidic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 81
- 239000003242 anti bacterial agent Substances 0.000 title claims abstract description 15
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims abstract description 184
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims abstract description 78
- 230000002378 acidificating effect Effects 0.000 claims abstract description 73
- 229920001661 Chitosan Polymers 0.000 claims abstract description 63
- 241000894006 Bacteria Species 0.000 claims abstract description 53
- FHSWKZUNNVWBSG-UHFFFAOYSA-M 2-[3-[(4-amino-2-methylpyrimidin-5-yl)methyl]-4-methyl-1,3-thiazol-3-ium-5-yl]ethanol;dodecyl hydrogen sulfate;dodecyl sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O.CCCCCCCCCCCCOS([O-])(=O)=O.CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N FHSWKZUNNVWBSG-UHFFFAOYSA-M 0.000 claims abstract description 52
- 230000000844 anti-bacterial effect Effects 0.000 claims abstract description 46
- 239000004310 lactic acid Substances 0.000 claims abstract description 39
- 235000014655 lactic acid Nutrition 0.000 claims abstract description 39
- 238000000034 method Methods 0.000 claims abstract description 15
- 244000005700 microbiome Species 0.000 claims abstract description 14
- 239000004480 active ingredient Substances 0.000 claims abstract description 5
- 235000011194 food seasoning agent Nutrition 0.000 claims description 27
- 235000013305 food Nutrition 0.000 claims description 21
- 238000004321 preservation Methods 0.000 claims description 3
- 229960000583 acetic acid Drugs 0.000 abstract description 59
- 235000011054 acetic acid Nutrition 0.000 abstract description 58
- 230000001747 exhibiting effect Effects 0.000 abstract description 2
- 229960000448 lactic acid Drugs 0.000 abstract 1
- 238000012360 testing method Methods 0.000 description 34
- 239000003921 oil Substances 0.000 description 24
- 235000019198 oils Nutrition 0.000 description 24
- 239000012071 phase Substances 0.000 description 18
- 239000000796 flavoring agent Substances 0.000 description 16
- 235000019634 flavors Nutrition 0.000 description 16
- 238000002360 preparation method Methods 0.000 description 12
- 235000002639 sodium chloride Nutrition 0.000 description 12
- 239000000243 solution Substances 0.000 description 12
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 11
- 239000000052 vinegar Substances 0.000 description 11
- 235000021419 vinegar Nutrition 0.000 description 11
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 10
- 239000008346 aqueous phase Substances 0.000 description 10
- 239000007788 liquid Substances 0.000 description 10
- 239000004278 EU approved seasoning Substances 0.000 description 9
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 150000001982 diacylglycerols Chemical class 0.000 description 8
- 230000001580 bacterial effect Effects 0.000 description 7
- 238000002156 mixing Methods 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 229920001817 Agar Polymers 0.000 description 6
- 241000186839 Lactobacillus fructivorans Species 0.000 description 6
- 239000008272 agar Substances 0.000 description 6
- 239000002504 physiological saline solution Substances 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 6
- 239000011780 sodium chloride Substances 0.000 description 6
- 241000233866 Fungi Species 0.000 description 5
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- JZRWCGZRTZMZEH-UHFFFAOYSA-N Thiamine Natural products CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N JZRWCGZRTZMZEH-UHFFFAOYSA-N 0.000 description 4
- 239000003814 drug Substances 0.000 description 4
- 239000003925 fat Substances 0.000 description 4
- 235000019197 fats Nutrition 0.000 description 4
- 238000012423 maintenance Methods 0.000 description 4
- 229960003495 thiamine Drugs 0.000 description 4
- 229920002101 Chitin Polymers 0.000 description 3
- 241000238557 Decapoda Species 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 241000186605 Lactobacillus paracasei Species 0.000 description 3
- 240000006024 Lactobacillus plantarum Species 0.000 description 3
- 240000008415 Lactuca sativa Species 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 235000015165 citric acid Nutrition 0.000 description 3
- 239000002537 cosmetic Substances 0.000 description 3
- 210000004748 cultured cell Anatomy 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical group CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 3
- 229940043264 dodecyl sulfate Drugs 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 229940093915 gynecological organic acid Drugs 0.000 description 3
- 150000007524 organic acids Chemical class 0.000 description 3
- 235000005985 organic acids Nutrition 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 239000000523 sample Substances 0.000 description 3
- 229910001961 silver nitrate Inorganic materials 0.000 description 3
- 230000001954 sterilising effect Effects 0.000 description 3
- 238000004659 sterilization and disinfection Methods 0.000 description 3
- 235000019640 taste Nutrition 0.000 description 3
- 235000019157 thiamine Nutrition 0.000 description 3
- 239000011721 thiamine Substances 0.000 description 3
- MFCMBWRHOUCXEZ-CAHLUQPWSA-N 3-aminopropyl [(2r)-2-[(1s)-1,2-dihydroxyethyl]-3-hydroxy-5-oxo-2h-furan-4-yl] hydrogen phosphate Chemical compound NCCCOP(O)(=O)OC1=C(O)[C@@H]([C@@H](O)CO)OC1=O MFCMBWRHOUCXEZ-CAHLUQPWSA-N 0.000 description 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 241000186660 Lactobacillus Species 0.000 description 2
- 240000001929 Lactobacillus brevis Species 0.000 description 2
- 241000598963 Lactobacillus fructivorans KCTC 3543 = DSM 20203 Species 0.000 description 2
- 235000013965 Lactobacillus plantarum Nutrition 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical group [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 240000007594 Oryza sativa Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical group [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 229930003451 Vitamin B1 Natural products 0.000 description 2
- 238000006640 acetylation reaction Methods 0.000 description 2
- 239000010775 animal oil Substances 0.000 description 2
- 230000000845 anti-microbial effect Effects 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 229940039696 lactobacillus Drugs 0.000 description 2
- 229940072205 lactobacillus plantarum Drugs 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000008268 mayonnaise Substances 0.000 description 2
- 235000010746 mayonnaise Nutrition 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000006072 paste Substances 0.000 description 2
- 230000001766 physiological effect Effects 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 235000009566 rice Nutrition 0.000 description 2
- 235000012045 salad Nutrition 0.000 description 2
- 239000012488 sample solution Substances 0.000 description 2
- 238000005070 sampling Methods 0.000 description 2
- 235000015067 sauces Nutrition 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 235000014347 soups Nutrition 0.000 description 2
- 239000003826 tablet Substances 0.000 description 2
- KYMBYSLLVAOCFI-UHFFFAOYSA-N thiamine Chemical compound CC1=C(CCO)SCN1CC1=CN=C(C)N=C1N KYMBYSLLVAOCFI-UHFFFAOYSA-N 0.000 description 2
- DPJRMOMPQZCRJU-UHFFFAOYSA-M thiamine hydrochloride Chemical compound Cl.[Cl-].CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N DPJRMOMPQZCRJU-UHFFFAOYSA-M 0.000 description 2
- 238000004448 titration Methods 0.000 description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 description 2
- 239000008158 vegetable oil Substances 0.000 description 2
- 235000010374 vitamin B1 Nutrition 0.000 description 2
- 239000011691 vitamin B1 Substances 0.000 description 2
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- QLOKJRIVRGCVIM-UHFFFAOYSA-N 1-[(4-methylsulfanylphenyl)methyl]piperazine Chemical compound C1=CC(SC)=CC=C1CN1CCNCC1 QLOKJRIVRGCVIM-UHFFFAOYSA-N 0.000 description 1
- 235000001674 Agaricus brunnescens Nutrition 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- 241000238366 Cephalopoda Species 0.000 description 1
- 208000035473 Communicable disease Diseases 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 241000238424 Crustacea Species 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 235000013957 Lactobacillus brevis Nutrition 0.000 description 1
- 241000186679 Lactobacillus buchneri Species 0.000 description 1
- 235000003228 Lactuca sativa Nutrition 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 244000294411 Mirabilis expansa Species 0.000 description 1
- 235000015429 Mirabilis expansa Nutrition 0.000 description 1
- 241000908267 Moniliella Species 0.000 description 1
- MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- 235000019485 Safflower oil Nutrition 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 235000019486 Sunflower oil Nutrition 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 241000235029 Zygosaccharomyces bailii Species 0.000 description 1
- 230000021736 acetylation Effects 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 235000013334 alcoholic beverage Nutrition 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 235000019606 astringent taste Nutrition 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 235000019658 bitter taste Nutrition 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- RQFQJYYMBWVMQG-IXDPLRRUSA-N chitotriose Chemical compound O[C@@H]1[C@@H](N)[C@H](O)O[C@H](CO)[C@H]1O[C@H]1[C@H](N)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)N)[C@@H](CO)O1 RQFQJYYMBWVMQG-IXDPLRRUSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
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- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 238000012258 culturing Methods 0.000 description 1
- 235000013365 dairy product Nutrition 0.000 description 1
- 230000000850 deacetylating effect Effects 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 235000015872 dietary supplement Nutrition 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000007884 disintegrant Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 150000002148 esters Chemical group 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 235000021323 fish oil Nutrition 0.000 description 1
- 238000009920 food preservation Methods 0.000 description 1
- 235000013611 frozen food Nutrition 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 235000013536 miso Nutrition 0.000 description 1
- 150000002759 monoacylglycerols Chemical class 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- -1 normal salt Chemical class 0.000 description 1
- 150000007523 nucleic acids Chemical class 0.000 description 1
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- 238000001139 pH measurement Methods 0.000 description 1
- 239000003346 palm kernel oil Substances 0.000 description 1
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- 239000002540 palm oil Substances 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 239000000419 plant extract Substances 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 235000020991 processed meat Nutrition 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 235000021067 refined food Nutrition 0.000 description 1
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- 235000015170 shellfish Nutrition 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 235000013555 soy sauce Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
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- 235000013599 spices Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
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- 239000002600 sunflower oil Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 150000003544 thiamines Chemical class 0.000 description 1
- DCXXMTOCNZCJGO-UHFFFAOYSA-N tristearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
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Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A40/00—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production
- Y02A40/90—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production in food processing or handling, e.g. food conservation
Landscapes
- Food Preservation Except Freezing, Refrigeration, And Drying (AREA)
- Seasonings (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
本発明は、酢酸耐性微生物、特に酢酸耐性乳酸菌に対して優れた抗菌作用を有し、酸性組成物に適した抗菌剤組成物、並びに酸性組成物の抗菌又は保存方法に関する。 The present invention relates to an antibacterial agent composition having an excellent antibacterial action against an acetic acid resistant microorganism, particularly an acetic acid resistant lactic acid bacterium, and suitable for an acidic composition, and an antibacterial or preserving method of the acidic composition.
抗菌性物質は、微生物による製品の汚染や変質の防止又は感染症の予防などのため、化粧品、医薬品、食品、日用品などの製品に広く配合されており、品質管理や公衆衛生の面から非常に有用である。このような抗菌性物質には、銅、銀及び亜鉛などの金属イオン化させた無機系物質、第四級アンモニウム塩、プロピオン酸及び安息香酸などの有機合成系物質、天然系物質などが知られている。
特に食品においては高い安全性が求められており、消費者のニーズとして健康志向の観点からも天然系のものが好まれる。例えば、キトサンは、エビ、カニなどの甲殻類に含まれるキチンを脱アセチル化して得られる多糖類であり、細菌等に対し優れた抗菌作用を発揮することから広く利用されている。また、チアミンラウリル硫酸塩は、ビタミンB1としての生理活性に加えて、カビや酵母などに対し優れた抗菌作用を発揮し、食品の日持ち剤として利用されている。キトサンとチアミンラウリル硫酸塩に、さらに可溶化成分として乳酸、酢酸ナトリウム及びエチルアルコールを配合した食品保存用水溶液組成物が、米飯における一般菌数、酵母及び大腸菌数の増殖を抑制することも報告されている(特許文献1)。
Antibacterial substances are widely used in products such as cosmetics, pharmaceuticals, foods, and daily necessities to prevent contamination and alteration of products by microorganisms or to prevent infectious diseases. Useful. Examples of such antibacterial substances include metal ionized inorganic substances such as copper, silver and zinc, organic synthetic substances such as quaternary ammonium salts, propionic acid and benzoic acid, and natural substances. Yes.
In particular, foods are required to have high safety, and natural products are preferred from the viewpoint of health as consumers' needs. For example, chitosan is a polysaccharide obtained by deacetylating chitin contained in crustaceans such as shrimps and crabs, and is widely used because it exhibits an excellent antibacterial action against bacteria and the like. Thiamine lauryl sulfate, in addition to the physiological activity as vitamin B1, exhibits an excellent antibacterial action against molds and yeasts, and is used as a food shelf life. It has also been reported that an aqueous composition for food preservation containing chitosan and thiamine lauryl sulfate and lactic acid, sodium acetate and ethyl alcohol as solubilizing components suppresses the growth of the number of general bacteria, yeast and coliforms in cooked rice. (Patent Document 1).
一方、ラクトバチルス・フルクチボランス(Lactobacillus fructivorans)に代表される酢酸耐性乳酸菌は、耐熱・耐塩・好酢酸性の性質を持ち、しばしば酸性食品の変敗を引き起こすことが知られている(非特許文献1)。酢酸耐性乳酸菌の増殖は、通常、加熱殺菌、特数値(塩分濃度、酢酸濃度)において制御可能であることが知られているが、近年、消費者の嗜好性の多様化が進み、減塩志向からも塩味が少なく、また酸味も抑えられたマイルドな風味を求める風潮が高まっており、特数値が緩和され内容液の耐菌性が低下しているため、低塩・低酸味の食品において酢酸耐性乳酸菌の増殖を抑制することが一層重要となる。
前記キトサンは、酢酸を配合したマヨネーズ中のラクトバチルス・フルクチボランスに対し抗菌作用を発揮することが報告されている(非特許文献2)。
On the other hand, acetic acid-resistant lactic acid bacteria represented by Lactobacillus fructivorans have heat-resistant, salt-resistant and acetic acid-resistant properties, and are often known to cause deterioration of acidic foods (Non-patent Document 1). ). The growth of acetic acid-resistant lactic acid bacteria is usually known to be controllable by heat sterilization and specific values (salinity concentration, acetic acid concentration). As a result, there is an increasing trend to demand a mild flavor with less saltiness and reduced acidity, and the special values are relaxed and the bacteria resistance of the liquid content is reduced. It is even more important to suppress the growth of resistant lactic acid bacteria.
The chitosan has been reported to exhibit an antibacterial action against Lactobacillus fructivorans in mayonnaise containing acetic acid (Non-patent Document 2).
しかしながら、抗菌性物質には、苦味やエグ味、渋味を呈するものが多く、たとえ酢酸耐性乳酸菌の増殖抑制作用を有する抗菌性物質であっても酸性食品の風味を損なうものは使用できないか、使用できても配合量は制限されざるを得ないという問題がある。実際、前記キトサンも独特な不快な呈味を有するため、非特許文献2のように多量のキトサンを添加した場合はマヨネーズの風味が損なわれてしまい、さらには乳化安定性にも悪影響が生じることが判明した。
これまでに酸性食品本来の風味を損なうことなく、酢酸耐性乳酸菌を抗菌できる抗菌性物質は知られていない。
However, antibacterial substances often have a bitter taste, taste, astringency, even if they are antibacterial substances that inhibit the growth of acetic acid-resistant lactic acid bacteria and cannot impair the flavor of acidic foods, Even if it can be used, there is a problem that the blending amount must be limited. In fact, since the chitosan also has a unique unpleasant taste, when a large amount of chitosan is added as in Non-Patent Document 2, the flavor of mayonnaise is impaired, and further, the emulsion stability is adversely affected. There was found.
So far, no antibacterial substance capable of antibacterial acetic acid-resistant lactic acid bacteria without impairing the original flavor of acidic foods has been known.
本発明は、酸性組成物における酢酸耐性微生物、特に酢酸耐性乳酸菌に対して優れた抗菌作用を示す抗菌剤組成物、並びに酸性組成物の抗菌又は保存方法に関する。 The present invention relates to an antibacterial agent composition exhibiting an excellent antibacterial action against an acetic acid resistant microorganism, particularly an acetic acid resistant lactic acid bacterium in an acidic composition, and an antibacterial or preserving method of the acidic composition.
本発明者は、上記課題について検討したところ、キトサンとチアミンラウリル硫酸塩を併用することにより、酢酸耐性乳酸菌に対する抗菌作用が相乗的に増強され、キトサン単独、チアミンラウリル硫酸塩単独では効果が認められなかった低濃度においても酸性組成物における酢酸耐性乳酸菌の抗菌が可能であることを見出した。 The present inventor has examined the above problems, and by using chitosan and thiamine lauryl sulfate in combination, the antibacterial action against acetic acid-resistant lactic acid bacteria is synergistically enhanced, and chitosan alone and thiamine lauryl sulfate alone are effective. It was found that antibacterial activity of acetic acid-resistant lactic acid bacteria in acidic compositions was possible even at low concentrations.
すなわち、本発明は、キトサン及びチアミンラウリル硫酸塩を有効成分として含有する酸性組成物用抗菌剤組成物を提供するものである。
また、本発明は、キトサン及びチアミンラウリル硫酸塩を有効成分として含有する酢酸耐性微生物に対する抗菌剤組成物を提供するものである。
また、本発明は、酸性組成物に、キトサン及びチアミンラウリル硫酸塩を添加する酸性組成物の抗菌又は保存方法を提供するものである。
That is, the present invention provides an antibacterial agent composition for acidic compositions containing chitosan and thiamine lauryl sulfate as active ingredients.
Moreover, this invention provides the antibacterial agent composition with respect to the acetic acid tolerance microorganisms which contain a chitosan and thiamine lauryl sulfate as an active ingredient.
The present invention also provides an antibacterial or preservation method for an acidic composition in which chitosan and thiamine lauryl sulfate are added to the acidic composition.
本発明によれば、酸性組成物中の酢酸耐性乳酸菌の抗菌が可能であり、酸性組成物の変敗を防ぎ、保存性を向上させることができる。また、キトサンとチアミンラウリル硫酸塩の使用量を低減できることから酸性組成物の風味維持の点からも有用である。 ADVANTAGE OF THE INVENTION According to this invention, the antimicrobial of the acetic acid tolerance lactic acid bacteria in an acidic composition is possible, deterioration of an acidic composition can be prevented and a preservability can be improved. Moreover, since the usage-amount of chitosan and thiamine lauryl sulfate can be reduced, it is useful also from the point of the flavor maintenance of an acidic composition.
本発明で用いられるキトサンとしては、特に制限されず、カニやエビの甲殻類、昆虫などの外骨格、イカや貝類などの有機骨格、キノコ類やカビなどの細胞壁などに含まれるキチンをアルカリ・酸処理、酵素処理など公知の方法(例えば、内田泰著,“キチン,キトサンの抗菌性”,フードケミカル,No.2,p22(1988))にて脱Nアセチル化したもの、さらに酸、酵素などで加水分解した低分子キトサン、キトサンオリゴ糖などを用いることができる。また、キトサンは、水溶性ものが好ましい。 The chitosan used in the present invention is not particularly limited, and chitin contained in crab and shrimp crustaceans, exoskeletons such as insects, organic skeletons such as squids and shellfish, cell walls such as mushrooms and fungi, and so on. Deacetylated by known methods such as acid treatment and enzyme treatment (for example, Yasushi Uchida, “Anti-bacterial activity of chitin and chitosan”, Food Chemical, No. 2, p22 (1988)), and further acid and enzyme For example, low molecular chitosan hydrolyzed with chitosan oligosaccharide and the like can be used. Chitosan is preferably water-soluble.
キトサンの脱Nアセチル化度は50%以上が好ましく、70%以上がより好ましい。また、キトサンの重量平均分子量は、400,000以下、好ましくは1,000〜100,000、より好ましくは、2,000〜50,000、更に好ましくは、3,000〜20,000であるのが、酢酸耐性乳酸菌に対する抗菌効果及び酸性組成物の風味維持の点から好ましい。
キトサンは、「ハイシャンKG」(アサマ化成(株))などの市販品を用いることもできる。
The de-N-acetylation degree of chitosan is preferably 50% or more, and more preferably 70% or more. Moreover, the weight average molecular weight of chitosan is 400,000 or less, Preferably it is 1,000-100,000, More preferably, it is 2,000-50,000, More preferably, it is 3,000-20,000. Are preferred from the viewpoint of antibacterial effect against acetic acid resistant lactic acid bacteria and maintenance of flavor of acidic composition.
As the chitosan, a commercially available product such as “Hishan KG” (Asama Kasei Co., Ltd.) can also be used.
本発明で用いられるチアミンラウリル硫酸塩は、ビタミンB1誘導体の一種であり、ビタミンB1(チアミン)にラウリル硫酸がモル比1:2の比率で結合した化合物である。
本発明では、チアミンラウリル硫酸塩製剤として、「ビタゲン(登録商標)AS5」(田辺三菱製薬(株))、「デイプラス(登録商標)V」(上野製薬)、「トップサラダビタミンDL5」(奥野製薬工業(株))などの市販品を用いることができる。
Thiamine lauryl sulfate used in the present invention is a kind of vitamin B1 derivative, and is a compound in which lauryl sulfate is bound to vitamin B1 (thiamine) at a molar ratio of 1: 2.
In the present invention, as a thiamine lauryl sulfate preparation, “Vitagen (registered trademark) AS5” (Mitsubishi Tanabe Pharma Corporation), “Day Plus (registered trademark) V” (Ueno Pharmaceutical), “Top Salad Vitamin DL5” (Okuno) Commercial products such as Pharmaceutical Industry Co., Ltd. can be used.
後記実施例に示すように、キトサン及びチアミンラウリル硫酸塩を併用することによって、酢酸耐性乳酸菌に対して優れた抗菌作用を示す。ここで酢酸耐性乳酸菌とは、Lactobacillus属に属するラクトバチルス・フルクチボランス(L.fructivorans)、ラクトバチルス・ブチネリ(L.buchneri)、ラクトバチルス・ブレビス(L.brevis)、ラクトバチルス・プランタラム(L.plantarum)、ラクトバチルス・パラカセイ(L.paracasei)などが挙げられる。
なお、本発明において「抗菌」とは、微生物を死滅させる「殺菌」、「滅菌」、微生物の発生、発育、増殖を抑える「静菌」、「制菌」等いずれの概念も含む語である。
As shown in the Examples below, the combined use of chitosan and thiamine lauryl sulfate shows an excellent antibacterial action against acetic acid-resistant lactic acid bacteria. Here, the acetic acid resistant lactic acid bacteria are Lactobacillus fructivorans belonging to the genus Lactobacillus, L. buchneri, L. brevis, Lactobacillus plantarum (L. plantarum), Lactobacillus paracasei (L. paracasei) and the like.
In the present invention, the term “antibacterial” is a term that includes any concept such as “sterilization” that kills microorganisms, “sterilization”, “bacteriostasis” that suppresses the generation, growth, and growth of microorganisms, and “antibacterial”. .
また、キトサン及びチアミンラウリル硫酸塩を併用することによって、耐酢酸性の性質を有するカビ、酵母などの真菌、細菌などの酢酸耐性微生物に対しても優れた抗菌作用を示す。酢酸耐性微生物としては、具体的に、耐酢酸性酵母Zygosaccharomyces bailii、耐酢酸性カビMoniliella acetoabutansなどが挙げられる。
従って、キトサン及びチアミンラウリル硫酸塩を配合してなる組成物は、抗菌剤組成物として、当該微生物が増殖し得る酸性組成物の抗菌、保存性向上に有用である。また、キトサン及びチアミンラウリル硫酸塩を食品、医薬品、医薬部外品、化粧品などの製品に配合又は使用することにより、当該微生物に対する抗菌性を付与できる。
In addition, the combined use of chitosan and thiamine lauryl sulfate shows an excellent antibacterial action against acetic acid-resistant microorganisms such as fungi such as fungi such as yeast and yeast, and bacteria having acetic acid resistance. Specific examples of the acetic acid resistant microorganism include acetic acid resistant yeast Zygosaccharomyces bailii, acetic acid resistant mold Moniliella acetobutans.
Therefore, a composition comprising chitosan and thiamine lauryl sulfate is useful as an antibacterial agent composition for improving the antibacterial and storage stability of an acidic composition in which the microorganism can grow. Moreover, the antimicrobial property with respect to the said microorganisms can be provided by mix | blending or using chitosan and thiamine lauryl sulfate in products, such as a foodstuff, a pharmaceutical, a quasi-drug, and cosmetics.
本発明の抗菌剤組成物は、必要に応じて、例えば、他の抗菌性物質、賦形剤、結合剤、崩壊剤、滑沢剤、希釈剤、乳化剤、着色剤などを添加し、常法に従い、例えば、液状、粉末状、ペースト状、錠剤状、カプセル状、ジェル状などの任意の形態とすることができる。
キトサンとチアミンラウリル硫酸塩は、単一製剤としてもよく、別々に製剤化してセット(キット)として使用してもよい。また、この場合、キトサンとチアミンラウリル硫酸塩は同一の形態としなくてもよい。
The antibacterial agent composition of the present invention is added with other antibacterial substances, excipients, binders, disintegrants, lubricants, diluents, emulsifiers, colorants, and the like, if necessary. Accordingly, for example, it can be in any form such as liquid, powder, paste, tablet, capsule, and gel.
Chitosan and thiamine lauryl sulfate may be a single preparation, or may be formulated separately and used as a set (kit). In this case, chitosan and thiamine lauryl sulfate need not be in the same form.
本発明の抗菌剤組成物は、酢酸耐性乳酸菌に対する抗菌効果の点及び酸性組成物の風味維持の点から、酸性組成物中にキトサンが0.006質量%(以下、単に「%」とする)以上、より0.006〜0.054%、更に0.012〜0.054%、より更に0.018〜0.054%、殊更0.03〜0.042%となるように用いられるのが好ましい。また、同様の点から、酸性組成物中にチアミンラウリル硫酸塩が0.03%以上、より0.03〜0.06%、更に0.03〜0.05%、より更に0.035〜0.05%となるように用いられるのが好ましい。
酸性組成物におけるキトサンとチアミンラウリル硫酸塩の質量比は、酢酸耐性乳酸菌に対する抗菌効果の点から、3:1〜1:15、より2:1〜1:10、更に2:1〜1:3とするのが好ましい。
このとき、抗菌剤組成物を、酸性組成物中のキトサン及びチアミンラウリル硫酸塩の濃度が前記範囲となるようにそのまま用いてもよいが、キトサン及びチアミンラウリル硫酸塩を前記範囲よりも高含有とした抗菌剤組成物を前記任意の形態で調製し、酸性組成物に配合した後適宜希釈して、希釈後に前記範囲内となるように用いてもよい。希釈倍率は、5〜50質量倍、更に10〜40質量倍、より更に20〜30質量倍とすることが好ましい。希釈には、脱イオン水を無菌処理した水を用いるのが好ましい。
In the antibacterial agent composition of the present invention, chitosan is 0.006% by mass (hereinafter, simply referred to as “%”) in the acidic composition from the viewpoint of the antibacterial effect against acetic acid resistant lactic acid bacteria and the maintenance of the flavor of the acidic composition. As mentioned above, it is used so that it may become 0.006 to 0.054%, further 0.012 to 0.054%, still more 0.018 to 0.054%, especially 0.03 to 0.042%. preferable. Further, from the same point, thiamine lauryl sulfate in the acidic composition is 0.03% or more, more preferably 0.03 to 0.06%, further 0.03 to 0.05%, and still more 0.035 to 0. It is preferable to use it so that it may become 0.05%.
The mass ratio of chitosan and thiamine lauryl sulfate in the acidic composition is from 3: 1 to 1:15, more from 2: 1 to 1:10, more preferably from 2: 1 to 1: 3, from the viewpoint of the antibacterial effect against acetic acid resistant lactic acid bacteria. Is preferable.
At this time, the antibacterial agent composition may be used as it is so that the concentration of chitosan and thiamine lauryl sulfate in the acidic composition falls within the above range, but chitosan and thiamine lauryl sulfate are contained in a higher content than the above range. The prepared antibacterial agent composition may be prepared in the above-mentioned arbitrary form, mixed appropriately in the acidic composition, and then appropriately diluted, and used so as to be within the above range after dilution. The dilution factor is preferably 5 to 50 times, more preferably 10 to 40 times, and even more preferably 20 to 30 times. For dilution, it is preferable to use deionized water aseptically treated.
本発明において酸性組成物とは、酢酸耐性微生物が発生、発育、増殖し得る組成物であって、組成物のpH(組成物が油相部と水相部を有する場合は水相部のpH、20℃)が、7.0以下のものである。pHは、更に5.5以下、更に2〜4.5、より更に2.5〜4.1が好ましい。
酸性組成物が食品である場合、耐酢酸性が高いことが知られているラクトバチルス・フルクチボランスに対する抗菌効果を考慮すると、pHは4.1以下が好ましく、更に2〜4.1、より更に3.5〜4.1、殊更3.5〜3.9の範囲が好ましい。
In the present invention, an acidic composition is a composition in which acetic acid-resistant microorganisms can be generated, developed, and proliferated, and the pH of the composition (if the composition has an oil phase part and an aqueous phase part, the pH of the aqueous phase part). , 20 ° C.) is 7.0 or less. The pH is further preferably 5.5 or less, more preferably 2 to 4.5, and still more preferably 2.5 to 4.1.
When the acidic composition is a food, the antibacterial effect against Lactobacillus fructivorans, which is known to have high acetic acid resistance, is preferably 4.1 or less, more preferably 2 to 4.1, and even more 3 A range of .5 to 4.1, especially 3.5 to 3.9 is preferred.
酸性組成物としては、食品、医薬品、医薬部外品、化粧品などが例示されるが、好ましくは食品である。酸性の食品としては、例えば、乳製品、冷凍食品、インスタント食品、でんぷん加工製品、加工肉製品、その他加工食品、飲料、スープ類、調味料、栄養補助食品などが挙げられる。なかでも、各種つゆ類、各種たれ類、各種ソース類、各種ドレッシング類、味醂、ポン酢などの酸性液体調味料が好ましく、特に各種ドレッシング類が好ましい。ドレッシング類としては、水相部のみからなるもの、水相部と油相部を含有する非乳化型のもの(分離型)、水中油型の乳化物からなる乳化型のもの、又は水中油型の乳化物に油相を積層した分離型のものが挙げられる。具体的には、半固体状ドレッシング、乳化液状ドレッシング、分離液状ドレッシング、ドレッシングタイプ調味料、サラダ用調味料が挙げられる。 Examples of the acidic composition include foods, pharmaceuticals, quasi-drugs, cosmetics, etc., but foods are preferred. Examples of acidic foods include dairy products, frozen foods, instant foods, starch processed products, processed meat products, other processed foods, beverages, soups, seasonings, and nutritional supplements. Especially, acidic liquid seasonings, such as various soups, various sauces, various sauces, various dressings, miso, and ponzu, are preferable, and various dressings are especially preferable. As dressings, those comprising only an aqueous phase part, non-emulsifying type containing a water phase part and an oil phase part (separated type), an emulsion type comprising an oil-in-water emulsion, or an oil-in-water type And a separated type in which an oil phase is laminated on the emulsion. Specific examples include semi-solid dressings, emulsified liquid dressings, separated liquid dressings, dressing type seasonings, and salad seasonings.
酸性の食品が、水相部と油相部を含有する場合、油相部と水相部の質量比率は、5/95〜60/40であることが好ましく、更に10/80〜55/45、より更に10/85〜35/65であることが酢酸耐性乳酸菌に対する抗菌効果及び風味の点から好ましい。 When the acidic food contains an aqueous phase part and an oil phase part, the mass ratio of the oil phase part to the aqueous phase part is preferably 5/95 to 60/40, and more preferably 10/80 to 55/45. Further, 10/85 to 35/65 are preferable from the viewpoint of antibacterial effect and flavor against acetic acid resistant lactic acid bacteria.
ここで、油相部を形成する油相成分としては、食用油脂が主成分であり、例えば、動物油及び/又は植物油、並びにこれらを原料として加水分解後にグリセリンとエステル化反応した油脂、エステル交換油、水素添加油等が挙げられる。動物油としては、例えば牛脂、豚脂、魚油等が挙げられ、植物油としては、例えば大豆油、パーム油、パーム核油、綿実油、落花生油、ナタネ油、コーン油、サフラワー油、サンフラワー油、米油等が挙げられる。
また、油脂は、トリアシルグリセロール、ジアシルグリセロール、モノアシルグリセロールのいずれか1種以上を含むものとする。油脂は、ジアシルグリセロールを15%以上含むことが、生理効果の点から好ましい。油脂中のジアシルグリセロール含有量は、より15〜95%、更に35〜95%、より更に50〜95%、殊更70〜93%とすることが、同様の点から好ましい。
Here, as the oil phase component forming the oil phase part, edible fats and oils are the main components, for example, animal oils and / or vegetable oils, and oils and ester exchange oils that have been esterified with glycerol after hydrolysis using these as raw materials. And hydrogenated oil. Examples of animal oils include beef tallow, lard, fish oil and the like, and vegetable oils include, for example, soybean oil, palm oil, palm kernel oil, cottonseed oil, peanut oil, rapeseed oil, corn oil, safflower oil, sunflower oil, Rice oil etc. are mentioned.
The oil / fat contains at least one of triacylglycerol, diacylglycerol, and monoacylglycerol. The fat / oil preferably contains 15% or more of diacylglycerol from the viewpoint of physiological effects. It is preferable from the same point that the diacylglycerol content in the fat is more preferably 15 to 95%, further 35 to 95%, still more 50 to 95%, and particularly 70 to 93%.
酸性の食品には、野菜類、果実類、水、食酢、食塩、醤油、香辛料、糖、蛋白質素材、有機酸、アミノ酸系調味料、核酸系調味料、動植物エキス、発酵調味料、酒類、増粘剤、安定剤、乳化剤、着色料等の各種食品素材又は添加剤等を含んでいてよい。また、これらは、必要に応じて成形加工したものを使用してもよい。 Acidic foods include vegetables, fruits, water, vinegar, salt, soy sauce, spices, sugar, protein materials, organic acids, amino acid seasonings, nucleic acid seasonings, animal and plant extracts, fermented seasonings, alcoholic beverages, increases Various food materials or additives such as a viscosity agent, a stabilizer, an emulsifier, and a colorant may be included. Moreover, you may use what was shape | molded as needed.
組成物のpHを上記範囲に低下させるためには、食酢、クエン酸、リンゴ酸等の有機酸;リン酸等の無機酸等の酸味料を使用することができ、特に食酢、クエン酸を用いることが好ましい。食酢は、穀物酢、りんご酢、ビネガー類等様々な種類を用いることができる。 In order to lower the pH of the composition to the above range, organic acids such as vinegar, citric acid and malic acid; acidulants such as inorganic acids such as phosphoric acid can be used, and vinegar and citric acid are particularly used. It is preferable. Various types of vinegar can be used, such as grain vinegar, apple vinegar, and vinegar.
食酢の含有量は、酸性組成物中に3〜50%、より5〜30%、更に6〜26%であることが好ましい。また、酢酸の含有量は5〜10%程度が好ましい。
本発明の酸性組成物の酸度(酸性組成物が油相部を有する場合は水相部の酸度)は、0.15〜10%、より0.25〜6%、更に0.3〜3%であることが風味の点から好ましい。なお、「酸度」とは、測定の対象となる液体を0.1mol/Lの水酸化ナトリウムで滴定を行い、その終点の滴定量から次の式(1)により算出したもの(食酢の日本農林規格(平成9年9月3日農林水産省告示第1381号)を参考に酢酸相当酸度の質量%を導出したもの)をいう。
酸度=(a×v×f)/w×100 (1)
(a:0.1mol/Lの水酸化ナトリウム1mLに相当する酢酸量0.006g、v:0.1mol/Lの水酸化ナトリウムの使用量(mL)、f:0.1mol/Lの水酸化ナトリウムの力価、w:試料採取量(g))
酸度は、酢酸の他、グルコン酸、クエン酸等の各種有機酸のいずれを使用した場合でも、これら全ての酸を酢酸換算して得た値の試料質量中の百分率で表したものである。
The content of vinegar is preferably 3 to 50%, more preferably 5 to 30%, and even more preferably 6 to 26% in the acidic composition. The acetic acid content is preferably about 5 to 10%.
The acidity of the acidic composition of the present invention (when the acidic composition has an oil phase part, the acidity of the aqueous phase part) is 0.15 to 10%, more 0.25 to 6%, and further 0.3 to 3%. It is preferable from the point of flavor. “Acidity” means that the liquid to be measured is titrated with 0.1 mol / L sodium hydroxide and calculated by the following formula (1) from the end point titration (Japanese vinegar of vinegar) Standard (derived from mass% of acetic acid equivalent acidity with reference to the Ministry of Agriculture, Forestry and Fisheries Notification No. 1381 on September 3, 1997).
Acidity = (a × v × f) / w × 100 (1)
(A: 0.006 g of acetic acid corresponding to 1 mL of 0.1 mol / L sodium hydroxide, v: amount of sodium hydroxide used (mL) of 0.1 mol / L, f: 0.1 mol / L of hydroxide Sodium titer, w: Sampling amount (g))
Acidity is expressed as a percentage in the sample mass of a value obtained by converting all of these acids into acetic acid, regardless of whether acetic acid, gluconic acid, or various organic acids such as citric acid is used.
また、食塩の含有量は、酸性組成物(酸性組成物が油相部を有する場合は水相部)中に2.6%以上、より2.6〜15%、更に2.6〜11%、殊更3〜4.7%であることが風味の点、酢酸耐性乳酸菌に対する抗菌効果の点から好ましい。
食塩としては、並塩、天日塩、岩塩等様々な種類のものを用いることができ、その一部を塩化カリウムや硫酸マグネシウム等に置き換えたものも用いることができる。
The content of sodium chloride is 2.6% or more, 2.6 to 15%, and 2.6 to 11% in the acidic composition (in the case where the acidic composition has an oil phase part), 2.6% or more. In particular, it is preferably 3 to 4.7% from the viewpoint of flavor and antibacterial effect against acetic acid-resistant lactic acid bacteria.
As the salt, various kinds of salt such as normal salt, sun salt, rock salt, etc. can be used, and a part of which is replaced with potassium chloride, magnesium sulfate or the like can also be used.
本発明のキトサンとチアミンラウリル硫酸塩を用いて酸性組成物を抗菌、保存するには、これら成分を酸性組成物に添加すればよい。キトサンとチアミンラウリル硫酸塩は、酸性組成物中のそれぞれの濃度が前記範囲となるように添加するのが酢酸耐性乳酸菌に対する抗菌効果の点及び酸性組成物の風味維持の点から好ましい。 In order to antibacterial and preserve an acidic composition using chitosan and thiamine lauryl sulfate of the present invention, these components may be added to the acidic composition. Chitosan and thiamine lauryl sulfate are preferably added so that each concentration in the acidic composition falls within the above range from the viewpoint of antibacterial effect against acetic acid-resistant lactic acid bacteria and maintenance of the flavor of the acidic composition.
キトサンとチアミンラウリル硫酸塩を酸性組成物に添加する方法は、特に制限されず、これら成分を酸性組成物に接触させる方法が挙げられ、例えば、キトサンとチアミンラウリル硫酸塩を酸性組成物の表面や内部に塗布、注入、付着等したり、これら成分の溶液に酸性組成物を浸漬したりする方法などが挙げられる。また、酸性組成物を製造する際に、キトサンとチアミンラウリル硫酸塩を配合してもよい。
キトサンとチアミンラウリル硫酸塩は、例えば、液状、粉末状、ペースト状、錠剤状、カプセル状、ジェル状などの任意の形態で用いることができる。また、これらは同時に添加してもよいし、間隔を置いて別々に添加してもよい。
The method for adding chitosan and thiamine lauryl sulfate to the acidic composition is not particularly limited, and examples thereof include a method in which these components are brought into contact with the acidic composition. For example, chitosan and thiamine lauryl sulfate are added to the surface of the acidic composition. Examples thereof include a method of coating, pouring and adhering inside, and a method of immersing an acidic composition in a solution of these components. Moreover, when manufacturing an acidic composition, you may mix | blend chitosan and thiamine lauryl sulfate.
Chitosan and thiamine lauryl sulfate can be used in any form such as liquid, powder, paste, tablet, capsule, and gel. Moreover, these may be added simultaneously, and may be added separately at intervals.
〔酸度の測定〕
上記「食酢の日本農林規格(平成9年9月3日農林水産省告示第1381号)」に基づき酢酸相当酸度の質量%を導出した。
(Measurement of acidity)
Based on the above “Japanese Agricultural Standard for Vinegar (September 3, 1997, Ministry of Agriculture, Forestry and Fisheries Notification No. 1381)”, the mass% of acetic acid equivalent acidity was derived.
〔NaCl濃度の測定〕
モール法により測定した。試料をメスフラスコに秤量し、蒸留水を加えて定容としたものを試料溶液とした。試料溶液をメスピペットを用いて三角フラスコにとり、指示薬として1.0%クロム酸カリウム溶液を加え、0.1mol/l硝酸銀溶液で褐色ビュレットを用いて滴定し、液の色が微橙色になる点を終点とした。
NaCl濃度は下記の計算式で算出した。
NaCl濃度(%)=0.00585×A×F/W×100
A: 0.1mol/L硝酸銀溶液の滴定量(mL)
F:0.1mol/L硝酸銀溶液の力価
W:試料採取量(mL)
[Measurement of NaCl concentration]
It was measured by the molding method. A sample was weighed into a measuring flask, and distilled water was added to make a constant volume to make a sample solution. Take the sample solution into a Erlenmeyer flask using a measuring pipette, add 1.0% potassium chromate solution as an indicator, and titrate with a 0.1 mol / l silver nitrate solution using a brown burette, and the color of the solution becomes slightly orange Was the end point.
The NaCl concentration was calculated by the following formula.
NaCl concentration (%) = 0.00585 × A × F / W × 100
A: Titration volume of 0.1 mol / L silver nitrate solution (mL)
F: titer of 0.1 mol / L silver nitrate solution W: sampling amount (mL)
〔pHの測定〕
pHは、試料の品温を20℃にした後、(株)堀場製作所製pHメーター(F−22)を使用し測定した。
[Measurement of pH]
The pH was measured using a pH meter (F-22) manufactured by Horiba, Ltd. after the sample temperature was 20 ° C.
実施例1
(1)培地の調製
3質量%NaCl,0.5質量%酢酸加Nutrient broth 培地(5ml)をpH4.5に調整し、キトサン製剤(「ハイシャンKG」、キトサン含有量6質量%、アサマ化成(株)製)、チアミンラウリル硫酸塩製剤(「ビタゲンAS5」、田辺三菱製薬(株)社製)をそれぞれキトサン、チアミンラウリル硫酸塩の最終濃度が0〜0.015質量%になるように添加し試験用培地とした。
Example 1
(1) Preparation of medium 3% NaCl, 0.5% acetic acid-added neutral broth medium (5 ml) was adjusted to pH 4.5, chitosan preparation (“Hishan KG”, chitosan content 6% by mass, Asama Kasei ( Co., Ltd.) and thiamine lauryl sulfate preparation ("Vitagen AS5", manufactured by Mitsubishi Tanabe Pharma Co., Ltd.) are added so that the final concentrations of chitosan and thiamine lauryl sulfate are 0 to 0.015% by mass, respectively. A test medium was used.
(2)接触試験
試験菌として、酢酸耐性乳酸菌の中で特に耐酢酸性が高いことが知られているラクトバチルス・フルクチボランス JCM1117株を用いた。
ラクトバチルス・フルクチボランス JCM1117株はMRS寒天培地(OXOID)、30℃で嫌気的に3日間培養した。培養した菌体を生理食塩水に105〜6cfu/mlになるように調整して菌液とした。菌液を1700cfu/mlになるように試験用培地に添加し、強攪拌後30℃で4週間培養した。培養後、生理食塩水で希釈しMRS寒天培地(OXOID社製)に植菌して生存菌数を平板塗沫法にて測定した。結果を表1に示す。
(2) Contact test Lactobacillus fructivorans JCM1117 strain, which is known to have particularly high acetic acid resistance among acetic acid-resistant lactic acid bacteria, was used as a test bacterium.
Lactobacillus fructivorans strain JCM1117 was anaerobically cultured for 3 days at 30 ° C. in MRS agar medium (OXOID). The cultured cells were adjusted to 10 5 to 6 cfu / ml in physiological saline to obtain a bacterial solution. The bacterial solution was added to the test medium at 1700 cfu / ml, and after vigorous stirring, cultured at 30 ° C. for 4 weeks. After culturing, it was diluted with physiological saline, inoculated into MRS agar medium (manufactured by OXOID), and the number of viable bacteria was measured by a plate smearing method. The results are shown in Table 1.
表1に示すように、キトサンとチアミンラウリル硫酸塩を併用することで酢酸耐性乳酸菌の抗菌作用が相乗的に増強された。 As shown in Table 1, the combined use of chitosan and thiamine lauryl sulfate synergistically enhanced the antibacterial activity of acetic acid resistant lactic acid bacteria.
実施例2
(1)酸性調味料の調製
水相部の原料を表2に示した量で配合し、撹拌混合(ホモディスパー:特殊機化工業製)して均一に溶解した。そこにキトサン製剤を加えさらに撹拌混合して溶解して水相部を調製した。次に、調製した水相部を常温から加熱して80℃に到達してから4分間保持することにより殺菌処理を行った後、常温まで冷却した。
次いで、表2に示した量のチアミンラウリル硫酸塩をジアシルグリセロール(DAG)脱臭油に添加し、攪拌混合しながら60℃まで加温し、チアミンラウリル硫酸塩を完全に溶解させたあと、常温まで冷却し油相部を調製した。
容器に水相部:油相部を7:3の割合で充填することにより液状の分離型酸性調味料(試験例1−6)を調製した。なお、表2記載のキトサン製剤中のキトサン含量は6質量%であった。また、キトサンの脱Nアセチル化度は80〜90%であり、重量平均分子量はおよそ10,000であった。
Example 2
(1) Preparation of acidic seasoning The raw materials for the aqueous phase were blended in the amounts shown in Table 2, and stirred and mixed (Homodisper: manufactured by Special Machine Industries) to dissolve uniformly. A chitosan preparation was added thereto, and further stirred and mixed to dissolve to prepare an aqueous phase part. Next, after the prepared water phase part was heated from room temperature and reached 80 ° C. and held for 4 minutes, it was sterilized and then cooled to room temperature.
Next, thiamin lauryl sulfate in the amount shown in Table 2 was added to diacylglycerol (DAG) deodorized oil and heated to 60 ° C. with stirring and mixing to completely dissolve the thiamine lauryl sulfate, and then to room temperature. The oil phase part was prepared by cooling.
A liquid separation type acidic seasoning (Test Example 1-6) was prepared by filling the container with a water phase part: oil phase part at a ratio of 7: 3. The chitosan content in the chitosan preparation described in Table 2 was 6% by mass. Moreover, the de-N acetylation degree of chitosan was 80 to 90%, and the weight average molecular weight was about 10,000.
(2)接触試験
試験菌として、酢酸耐性乳酸菌の中で特に耐酢酸性が高いことが知られているラクトバチルス・フルクチボランス JCM1117株を用いた。
ラクトバチルス・フルクチボランス JCM1117株はMRS寒天培地(OXOID)、30℃で嫌気的に3日間培養した。培養した菌体を生理食塩水に105〜6cfu/mlになるように調整して菌液とした。なお、菌の最終濃度103cfu/mlとなるように分離型酸性調味料100gに上記菌液を1ml接種し、30℃で60日間好気的に保存し菌の挙動を確認した。菌数測定は、保存後の調味料を強攪拌して系内を均一化した後、生理食塩水で希釈し、MRS寒天培地(OXOID社製)に塗抹して測定した。菌濃度として1オーダー以上の増殖が確認された場合を「増殖」、1オーダー未満の増殖が確認された場合を「非増殖」と判断した。結果を表3に示す。
(2) Contact test Lactobacillus fructivorans JCM1117 strain, which is known to have particularly high acetic acid resistance among acetic acid-resistant lactic acid bacteria, was used as a test bacterium.
Lactobacillus fructivorans strain JCM1117 was anaerobically cultured for 3 days at 30 ° C. in MRS agar medium (OXOID). The cultured cells were adjusted to 10 5 to 6 cfu / ml in physiological saline to obtain a bacterial solution. In addition, 1 ml of the above bacterial solution was inoculated into 100 g of the separated acidic seasoning so that the final concentration of the fungus was 10 3 cfu / ml, and stored aerobically at 30 ° C. for 60 days to confirm the behavior of the fungus. The number of bacteria was measured by thoroughly stirring the preserved seasoning to homogenize the system, diluting with physiological saline, and smearing on MRS agar medium (manufactured by OXOID). The case where growth of 1 order or more was confirmed as the bacteria concentration was judged as “growth”, and the case where growth of less than 1 order was confirmed as “non-growth”. The results are shown in Table 3.
表3から明らかなように、キトサン及びチアミンラウリル硫酸塩を特定量配合した試験例1−4では、酢酸耐性乳酸菌の増殖が見られず、酢酸耐性乳酸菌に対する抗菌作用が認められた。これに対し、pHが高い試験例5及び6ではキトサン及びチアミンラウリル硫酸塩の配合濃度が試験例1−4と同じであったが、酢酸耐性乳酸菌増殖が見られた。 As is apparent from Table 3, in Test Examples 1-4 in which specific amounts of chitosan and thiamine lauryl sulfate were blended, no growth of acetic acid resistant lactic acid bacteria was observed, and an antibacterial action against acetic acid resistant lactic acid bacteria was observed. In contrast, in Test Examples 5 and 6 having a high pH, the blending concentrations of chitosan and thiamine lauryl sulfate were the same as in Test Example 1-4, but acetic acid-resistant lactic acid bacterium growth was observed.
実施例3
実施例1と同様にして、表4に示した配合で液状の分離型酸性調味料(試験例7−10)を調製した。
Example 3
In the same manner as in Example 1, a liquid separation-type acidic seasoning (Test Examples 7-10) having the composition shown in Table 4 was prepared.
調製したそれぞれの分離型酸性調味料(試験例7−10)について実施例1と同様に、接触試験を行った。結果を表5に示す。 A contact test was conducted in the same manner as in Example 1 for each of the prepared separate acidic seasonings (Test Examples 7-10). The results are shown in Table 5.
表5から明らかなように、キトサン及びチアミンラウリル硫酸塩を特定量配合した試験例8及び9では、酢酸耐性乳酸菌の増殖が見られず、酢酸耐性乳酸菌に対する抗菌作用が認められた。これに対し、キトサン及びチアミンラウリル硫酸塩を配合しなかった試験例7では、酢酸耐性乳酸菌増殖が認められた。また、酸性調味料のpHが高い試験例10では酢酸耐性乳酸菌増殖が認められた。 As is clear from Table 5, in Test Examples 8 and 9 containing a specific amount of chitosan and thiamine lauryl sulfate, no growth of acetic acid resistant lactic acid bacteria was observed, and an antibacterial action against the acetic acid resistant lactic acid bacteria was observed. In contrast, in Test Example 7 in which chitosan and thiamine lauryl sulfate were not blended, acetic acid-resistant lactic acid bacteria were observed to grow. In Test Example 10 where the pH of the acidic seasoning is high, acetic acid-resistant lactic acid bacterium growth was observed.
実施例4
(1)酸性調味料の調製
キトサン及びチアミンラウリル硫酸塩の配合量をかえた以外は表2の試験例1の調味料と同様の組成で液状の分離型酸性調味料(試験例11−27)を調製した。
調製したそれぞれの分離型酸性調味料(試験例11−27)について実施例1と同様に、接触試験を行った。結果を表6に示す。
Example 4
(1) Preparation of acidic seasoning Liquid separation type acidic seasoning having the same composition as the seasoning of Test Example 1 in Table 2 except for changing the blending amounts of chitosan and thiamine lauryl sulfate (Test Examples 11-27) Was prepared.
A contact test was conducted in the same manner as in Example 1 for each of the prepared separate acidic seasonings (Test Examples 11-27). The results are shown in Table 6.
表6から明らかなように、キトサン及びチアミンラウリル硫酸塩を特定量配合した試験例12〜17では、酢酸耐性乳酸菌に対する抗菌作用が認められた。これに対し、キトサン及びチアミンラウリル硫酸塩を配合しなかった試験例11では、酢酸耐性乳酸菌増殖が認められた。また、キトサン又はチアミンラウリル硫酸塩を単独で特定濃度配合した試験例18〜23では、酢酸耐性乳酸菌増殖が認められた。単独での配合で酢酸耐性乳酸菌増殖が認められた濃度以下のキトサン及びチアミンラウリル硫酸塩を同時に配合した試験例24〜27では酢酸耐性乳酸菌に対する抗菌作用が認められた。 As is clear from Table 6, in Test Examples 12 to 17 in which specific amounts of chitosan and thiamine lauryl sulfate were blended, an antibacterial action against acetic acid resistant lactic acid bacteria was observed. On the other hand, in Test Example 11 in which chitosan and thiamine lauryl sulfate were not blended, acetic acid resistant lactic acid bacteria were observed to grow. In Test Examples 18 to 23, in which chitosan or thiamine lauryl sulfate alone was blended at a specific concentration, growth of acetic acid-resistant lactic acid bacteria was observed. In Test Examples 24 to 27 in which chitosan and thiamine lauryl sulfate at a concentration equal to or less than the concentration at which acetic acid-resistant lactic acid bacteria were found to be grown alone were combined, an antibacterial action against acetic acid-resistant lactic acid bacteria was observed.
実施例5
(1)酸性調味料の調製
水相部の原料を表7に示した量で配合し、撹拌混合(ホモディスパー:特殊機化工業製)して均一に溶解した。そこにキトサン製剤を加えさらに撹拌混合して溶解して水相部を調製した。次に、調製した水相部を常温から加熱して80℃に到達してから4分間保持することにより殺菌処理を行った後、常温まで冷却した。
次いで、表7に示した量のチアミンラウリル硫酸塩をジアシルグリセロール(DAG)脱臭油に添加し、攪拌混合しながら60℃まで加温し、チアミンラウリル硫酸塩を完全に溶解させたあと、常温まで冷却し油相部を調製した。
水相部と油相部を7:3の割合で混合し、乳化機(T.K.ホモディスパー2.5型:プライミクス(株))を用いて乳化型の酸性調味料(試験例28−34)を調製した。
Example 5
(1) Preparation of acidic seasoning The raw materials for the aqueous phase were blended in the amounts shown in Table 7, and stirred and mixed (Homodisper: manufactured by Special Machine Industries) to dissolve uniformly. A chitosan preparation was added thereto, and further stirred and mixed to dissolve to prepare an aqueous phase part. Next, after the prepared water phase part was heated from room temperature and reached 80 ° C. and held for 4 minutes, it was sterilized and then cooled to room temperature.
Next, thiamine lauryl sulfate in the amount shown in Table 7 was added to diacylglycerol (DAG) deodorized oil, heated to 60 ° C. with stirring and mixing, and thiamine lauryl sulfate was completely dissolved, then to room temperature. The oil phase part was prepared by cooling.
The water phase part and the oil phase part were mixed at a ratio of 7: 3, and the emulsification type acid seasoning (Test Example 28-) was conducted using an emulsifier (TK Homodisper 2.5 type: Primix Co., Ltd.). 34) was prepared.
(2)接触試験
試験菌として、ラクトバチルス・ブチネリJCM1115株、ラクトバチルス・ブレビス JCM1059株、ラクトバチルス・プランタラム JCM1149株、ラクトバチルス・パラカセイ 土壌単離株の4菌種を用いた。
菌はMRS寒天培地(OXOID)、30℃で嫌気的に3日間培養した。培養した菌体を4菌株の菌数が均等になるように混合し、生理食塩水に合計菌数が105〜6cfu/mlになるように調整して菌液とした。菌の最終濃度103cfu/mlとなるように乳化型酸性調味料100gに上記菌液を1ml接種し、30℃で60日間好気的に保存し菌の挙動を確認した。菌数測定は、保存後の調味料を強攪拌して系内を均一化した後、生理食塩水で希釈し、MRS寒天培地(OXOID社製)に塗抹して測定した。菌濃度として1オーダー以上の増殖が確認された場合を「増殖」、1オーダー未満の増殖が確認された場合を「非増殖」と判断した。結果を表8及び9に示す。
(2) Contact test As test bacteria, 4 strains of Lactobacillus butinelli JCM1115 strain, Lactobacillus brevis JCM1059 strain, Lactobacillus plantarum JCM1149 strain, and Lactobacillus paracasei soil isolate were used.
The bacteria were anaerobically cultured for 3 days at 30 ° C. in MRS agar medium (OXOID). The cultured cells were mixed so that the numbers of the four bacterial strains were equal, and adjusted to a total of 10 5 to 6 cfu / ml in physiological saline to obtain a bacterial solution. 1 ml of the above bacterial solution was inoculated into 100 g of the emulsified acidic seasoning so that the final concentration of the bacteria was 10 3 cfu / ml, and aerobically stored at 30 ° C. for 60 days to confirm the behavior of the bacteria. The number of bacteria was measured by thoroughly stirring the preserved seasoning to homogenize the system, diluting with physiological saline, and smearing on MRS agar medium (manufactured by OXOID). The case where growth of 1 order or more was confirmed as the bacteria concentration was judged as “growth”, and the case where growth of less than 1 order was confirmed as “non-growth”. The results are shown in Tables 8 and 9.
表8から明らかなように、キトサン及びチアミンラウリル硫酸塩を特定量配合した試験例28−32では酢酸耐性乳酸菌に対する抗菌作用が認められ、これに対し、表9に示されるように、キトサン及びチアミンラウリル硫酸塩を配合しなかった試験例33、チアミンラウリル硫酸塩の配合量が少なかった試験例34では、酢酸耐性乳酸菌増殖が認められた。 As is apparent from Table 8, in Test Examples 28-32 containing a specific amount of chitosan and thiamine lauryl sulfate, an antibacterial action against acetic acid-resistant lactic acid bacteria was observed, whereas, as shown in Table 9, chitosan and thiamine. In Test Example 33 in which lauryl sulfate was not blended and in Test Example 34 in which the blending amount of thiamine lauryl sulfate was small, growth of acetic acid-resistant lactic acid bacteria was observed.
実施例6
(1)酸性調味料の調製
市販のノンオイルドレッシングに、表10に示す濃度になるようにキトサン、チアミンラウリル硫酸塩及びDAG脱臭油を特定量配合し、分離型酸性調味料(試験例35−40)を調製した。
Example 6
(1) Preparation of acidic seasoning In a commercially available non-oil dressing, chitosan, thiamine lauryl sulfate and DAG deodorized oil are blended in specific amounts so as to have the concentrations shown in Table 10, and a separate acidic seasoning (Test Example 35-40). ) Was prepared.
(2)官能評価
市販レタス40gに、分離型酸性調味料を15gかけ、パネル3名による食味試験を行い、協議により評点を決定した。
評価は、以下に示す基準に従って行った。すなわち、無添加のものと風味上差がない場合は○(合格)、風味に差があるが許容できる場合は△(合格)、風味上許容できない場合は×(不合格)とした。結果を表11に示す。
(2) Sensory evaluation 15 g of a separate acidic seasoning was applied to 40 g of commercially available lettuce, a taste test was conducted by three panelists, and a score was determined through consultation.
Evaluation was performed according to the following criteria. That is, when there was no difference in flavor from the additive-free one, the result was ○ (passed), when there was a difference in the flavor but was acceptable, Δ (passed), and when the flavor was not acceptable, × (failed). The results are shown in Table 11.
表11から明らかなように、キトサン及びチアミンラウリル硫酸塩を、酢酸耐性乳酸菌を抗菌できる濃度範囲で配合した試験例35−38では風味上問題がなかった、これに対し、キトサン及びチアミンラウリル硫酸塩を高濃度配合した試験例39及び40は、苦渋みがあり風味上許容できるものではなかった。 As is apparent from Table 11, there was no problem in flavor in Test Examples 35 to 38 in which chitosan and thiamine lauryl sulfate were blended in a concentration range in which acetic acid-resistant lactic acid bacteria can be antibacterial, whereas chitosan and thiamine lauryl sulfate were not. Test Examples 39 and 40 in which a high concentration was added were bitter and astringent and were not acceptable in flavor.
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