CZ302175B6 - Mutantní kmen Lactobacillus bulgaricus - Google Patents
Mutantní kmen Lactobacillus bulgaricus Download PDFInfo
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- CZ302175B6 CZ302175B6 CZ20004359A CZ20004359A CZ302175B6 CZ 302175 B6 CZ302175 B6 CZ 302175B6 CZ 20004359 A CZ20004359 A CZ 20004359A CZ 20004359 A CZ20004359 A CZ 20004359A CZ 302175 B6 CZ302175 B6 CZ 302175B6
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- 235000013960 Lactobacillus bulgaricus Nutrition 0.000 title claims abstract description 16
- 229940004208 lactobacillus bulgaricus Drugs 0.000 title claims abstract description 16
- 241000186672 Lactobacillus delbrueckii subsp. bulgaricus Species 0.000 title claims abstract 9
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- C12N1/00—Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
- C12N1/20—Bacteria; Culture media therefor
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23C—DAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING OR TREATMENT THEREOF
- A23C9/00—Milk preparations; Milk powder or milk powder preparations
- A23C9/12—Fermented milk preparations; Treatment using microorganisms or enzymes
- A23C9/123—Fermented milk preparations; Treatment using microorganisms or enzymes using only microorganisms of the genus lactobacteriaceae; Yoghurt
- A23C9/1238—Fermented milk preparations; Treatment using microorganisms or enzymes using only microorganisms of the genus lactobacteriaceae; Yoghurt using specific L. bulgaricus or S. thermophilus microorganisms; using entrapped or encapsulated yoghurt bacteria; Physical or chemical treatment of L. bulgaricus or S. thermophilus cultures; Fermentation only with L. bulgaricus or only with S. thermophilus
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12R—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
- C12R2001/00—Microorganisms ; Processes using microorganisms
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- C12R2001/225—Lactobacillus
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Abstract
Mutantní kmen Lactobacillus bulgaricus, uložený ve sbírce kultur CNCM 14. ledna 1998 pod císlem I-1968, nesoucí bodovou nonsense mutaci v kódové sekvenci pro .beta.-galaktosidázu a postrádající .beta.-galaktosidázovou aktivitu. Soucást rešení tvorí také mlécný zákvas, obsahující uvedený kmen, zpusob výroby zakvašeného mlécného výrobku pomocí tohoto zákvasu a výsledný zakvašený mlécný výrobek, zejména jogurt.
Description
Mutantní kmen Lactobacillus bulgaricus
Oblast techniky
Vynález se týká mutantního kmene Lactobacillus bulgaricus, uloženého ve sbírce kultur CNCM 14. ledna 1998 pod číslem 1-1968, nesoucího bodovou nonsense mutaci v kódové sekvenci pro β-galaktosidázu a postrádajícího β-galaktosidázovou aktivitu.
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Dosavadní stav techniky
Jogurty se běžně získávají kvašením mléka kombinací kmenů Streptococcus thermophilus a Lactobacillus bulgaricus. Během kvašení, které se provádí při tepiotě přibližně 40 až 45 °C, používají tyto bakterie jako energetický substrát především laktózu a produkují kyselinu mléčnou, která působí srážení mléka. Tento krok kvašení (nazývaný také „acidifikace oky selo vání“) je ukončen ochlazením výrobku, jakmile jeho pH dosáhne hodnoty přibližně 4,8 až 4,5. Výrobek se pak během zbylého výrobního procesu, procesu balení a až do doby konzumace uchovává v chladu.
Ochlazení samozřejmě nezastaví kvašení mléčné kyseliny úplně; dokonce i pokud je výrobek uchováván při 4 °C, je v průběhu času pozorováno postupné zvyšování jeho kyselosti.
Tento jev, známý jako postacidifikace, dodatečné okyselování, je zodpovědný za degradaci orga25 noleptických kvalit (týkajících se chuti a vůně) výrobku během jeho uchovávání.
Dodatečné okyselování je výsledkem zejména toho, že bakterie, zvláště L. bulgaricus, využívají laktózu, zbývající ve výrobku na konci řízeného kroku okyselování. K odstranění tohoto jevu bylo navrženo použití kmenů L. bulgaricus, které kvasí laktózu jen obtížně nebo vůbec.
Jedním z enzymů, které jsou pro kvašení laktózy nezbytné, je β-galaktosidáza, která hydrolyzuje laktózu na glukózu a galaktózu. Pro získání kmenů L. bulgaricus, nevytvářejících dodatečné okyselování, bylo proto navrženo vyrobit umělé mutanty, nebo vybrat přírodní mutanty, u nichž je aktivita tohoto enzymu nepříznivě ovlivněna.
Například patent EP 402 450 (Genencor) popisuje výrobu, prováděnou umístěnou mutagenezí genu β-galaktosidázy, podmíněných mutantů L. bulgaricus, u nichž β-galaktosidáza, která je aktivní během kvašení při 40 °C, ztrácí svou aktivitu při teplotě anebo při pH, které odpovídají podmínkám uchovávání kvašených mléčných výrobků.
Patentová přihláška JP 90053437 popisuje výrobu umělého mutantu L. bulgaricus, který zcela ztratil schopnost kvasit laktózu, a výběr přírodního mutantu se sníženou schopností kvasit laktózu; tyto mutanty jsou ovšem oba schopné normálního vývoje a okyselování v přítomnosti 5. thermophilus, pod podmínkou, že je médium doplněno glukózou. Vedlejší kultury takových mutantů zachovávají jejich charakteristiky okyselování, v mléku postrádajícím glukózu, i po deseti pasážování (subkulti vacích).
Patent EP 0518 096 (Societé des Produits Nestlé) navrhuje použít pro výrobu jogurtu chabě dodatečně okyselující mutanty L. bulgaricus, které byly předem vybrány podle kriteria delece (vypadnutí) fragmentu β-galaktosídázového genu. Plošné testování (screening) a charakterizace těchto mutantů je usnadněno skutečností, že přítomnost této delece může být snadno ověřena na restrikčních profilech.Navíc jsou delece známé jako nezvratné mutace, což umožňuje snadné získání stálých mutantních kmenů z rodičovského kmenu. Patent 0518 096 popisuje dva typy slabě dodatečně okyselujících mutantů, vybraných tímto způsobem. První vykazuje deleci, ovliv55 ftující pouze gen β-galaktosidázy; pokud jsou takové mutanty kombinovány se 5. thermophilus
- 1 CZ 302175 B6 a kultivovány na mléce, vykazují i bez přídavku glukózy růstové a oky sel uj ící vlastnosti, které jsou srovnatelné s týmiž vlastnostmi u divokých kmenů, z nichž pocházejí. Druhý typ vykazuje širší deleci, prostírající se po genu β-galaktosidázy v rozsahu nejméně lkb; pokud jsou takové mutanty kombinovány se V thermophilus, rostou mnohem pomaleji a mnohem méně okyselují než divoké kmeny, z nichž pocházejí. Přidání glukózy do kultivačního média mělo na jejich okyselující a dodatečně okysel uj ící vlastnosti pouze slabý vliv.
Přírodní mutanty, u nichž je β-galaktosidáza neaktivní, je mnohem obtížnější vybrat a udržovat jako čisté kultury v případě bodových mutací než v případě delečních mutací; to se vysvětluje nižší pravděpodobností bodových mutací, vytvářejících neaktivní bílkovinu, větší obtížností lokalizace a charakterizace bodových mutací za použití restrikčních profilů a velmi vysokou rychlostí zvratu.
Podstata vynálezu
Podstatu vynálezu tvoří mutantní kmen Laetobacillus bulgaricus, uložený ve sbírce kultur CNCM 14. ledna 1998 pod číslem 1-1968, nesoucí bodovou nonsense mutaci v kódové sekvenci pro βgalaktosidázu a postrádající β-galaktosidázovou aktivitu. Součást řešení tvoří také mléčný zákvas, obsahující uvedený kmen, způsob výroby zakvašeného výrobku pomocí tohoto zákvasu a výsledný zakvašený výrobek.
Kmen L. bulgaricus podle vynálezu byl uložen, podle Budapešťské smlouvy, 14. ledna 1998 v CNCM (Collection Nationale de Cultures de Mikroorganismem, Národní sbírce kultur mikroorganismů), uchovávané Pasteurovým ústavem v Paříži (Pasteur Institute, 25 rue du Dočteur Roux, Paris) pod číslem 1-1968.
Tento kmen má následující morfologické a biochemické charakteristiky:
- morfologie: Gram-positivní mikroorganismus, nepohyblivým, isolovaný nebo o krátkém řetězci, asporogenní, pleomorfní, tenké bacily;
- metabolismus: homofermentativní (samokvasný), kataláza(-);
- kvašení cukrů: D-glukóza (+), D-fruktóza (-), (D-mannóza (+), eskulin (+).
Autoři vynálezu sekvenovali laktózový operon mutantu 1-1968. Odpovídající sekvence je představována v připojeném seznamu sekvencí pod označením sekvence identifikačního Čísla 1 (sekv. id. č. 1). Sekvence translačních produktů (permeáza a β-galaktosidáza) jsou představovány pod označením sekv. id. č. 2 a sekv, id. č.3.
Analýza této sekvence odkryla dvě bodové mutace: jedna, v permeázovém genu (poloha 122 na sekvenci id. č. 1), indukuje výměnu aminokyseliny (Lys -> Asn); druhý, v genu β-galaktosidázy, (poloha 4519 na sekvenci id. č. 1) vkládá tzv. „stop-kodon“. Třebaže zachovává svá aktivní místa (polohy 464 a 531), je β-galaktosidáza produkovaná tímto mutantem inaktivní. Autoři vynálezu rovněž zaznamenali, že tato mutace zůstává stále po několika sériích pasážování, v kultivačním médiu obsahujícím glukózu. Na druhé straně v kultivačním médiu bez obsahu glukózy se tato nonsens ní mutace velmi rychle navrací do původního stavu (revertuje) tempem přibližně 10“6.
Předkládaný vynález rovněž zahrnuje mutantní kmeny, které jsou neschopné asimilovat laktózu a které jsou odvozeny od kmene 1-1968. Takové kmeny mohou být například získány indukováním jiných mutací na laktózovém operonu kmene 1-1968, místně řízenou mutagenezí.
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Předmětem tohoto vynálezu je rovněž mléčný zákvas, konkrétně jogurtový zákvas, který se vyznačuje tím, že zahrnuje alespoň jeden kmen L. bulgaricus podle vynálezu jak byl výše definován, s výhodou v kombinaci s alespoň jedním kmenem 5. thermophilus.
K produkci zákvasu podle vynálezu může být použit jakýkoli kmen 5. thermophilus, hodící se pro výrobu jogurtu; výběr jednoho nebo více kmenů S. thermophilus může být činěn jako funkce přídavných charakteristik, které je volitelně žádoucí poskytnout konečnému výrobku.
Jako příklad kmenů S. thermophilus, jež mohou být použity v kombinaci s kmenem L. bulgaricus io podle vynálezu, lze zmínit následující kmeny, uložené v CNCM (Collection Nationale de Cultures de Mikroorganismes, Národní sbírce kultur mikroorganismů), uchovávané Pasteurovým ústavem v Paříži (Pasteur Institute, 25 rue du Docteur Roux, Paris):
- kmen uložený 25. srpna 1994 pod číslem 1-1470 a kmen uložený 23. srpna 1995 pod číslem I15 1620; tyto dva kmeny jsou popsány v Evropské patentové přihlášce, zveřejněné pod číslem
96/06924;
-kmeny uložené 30. prosince 1994 pod čísly 1-1520 a 1-1521; tyto dva kmeny jsou popsány v PCT mezinárodní přihlášce WO 96/20607;
-kmen uložený 24. října 1995 pod číslem 1-1630; charakteristiky tohoto kmene jsou popsány v PCT mezinárodní přihlášce WO 96/01701.
Tyto kmeny mohou být kombinovány spolu navzájem anebo s jedním či více z dalších průmyslo25 vých kmenů S. thermophilus.
Kmen (kmeny) S. thermophilus je (jsou) kombinován (kombinovány) s kmenem (kmeny) L. bulgaricus podle vynálezu, stejným způsobem a ve stejných poměrech jako v běžných jogurtových zákvasech; populace bakterie L. bulgaricus podle vynálezu může například představovat 10 až
90 % a lépe 20 až 50 % celkové bakteriální populace.
Předmětem předkládaného vynálezu je také způsob výroby kvašeného mléčného výrobku, který se vyznačuje tím, že zahrnuje krok, během něhož se mléko kvasí za použití zákvasu, zahrnujícího alespoň jeden kmen L. bulgaricus podle vynálezu, v přítomnosti alespoň jednoho cukru, který může být asimilován uvedeným kmenem; zvláště se může jednak o fruktózu, mannózu, a s výhodou glukózu. Uvedený kvašený výrobek je s výhodou jogurt.
Způsob podle vynálezu je podobný běžným způsobům výroby jogurtu s ohledem na hlavní způsoby provedení kroku řízeného okyselování; konkrétně se toto okyselování provádí při teplotě mezi 20 a 45 °C a s výhodou mezi 30 a 45 °C, vsádkově, tj. v jediném kroku a za použití jednoho kvasného tanku.
Trvání tohoto kroku řízeného okyselování je obecně 6 až 24 hodin a s výhodou 6 až 16 hodin; je tedy delší než v případě běžných způsobů výroby jogurtů (kde je to 3 až 5 hodin při 44 °C).
Kmeny L. bulgaricus podle tohoto vynálezu, i v kombinaci se S. thermophilus, rostou a okyselují mnohem pomaleji než kmeny divokého typu.
Navíc se rychlost růstu a okyselování kmenů L. bulgaricus podle tohoto vynálezu liší velmi významně v závislosti na množství glukózy přidané do mléka. Tato vlastnost umožňuje řídit jejich růst a okyselování jednoduchým přidáním požadovaného množství glukózy na počátku kvašení.
Autoři vynálezu rovněž pozorovali, že pokud jsou použity kmeny L. bulgaricus nebo zákvas podle tohoto vynálezu, okyselování se značně zpomaluje, pokud pH dosáhne hodnot v rozmezí 4,8 až
4,5 (což odpovídá rozmezí hodnot pH, v němž je okyselování zastaveno v případě běžných způ-3CZ 302175 B6 sobů) a stabilizuje se, i když se mléko udržuje při teplotě kvašení, na minimálním pH. Hodnota tohoto minimálního pH zásadné závisí na množství přidané glukózy.
Tato vlastnost umožňuje snížit, nebo dokonce odstranit, fázi chlazeni, používanou v běžných způsobech výroby jogurtů k zastavení kvašení. Odstraňuje také nutnost měření pH pro stanovení optimálního okamžiku k zastavení kvašení; u daného zákvasu a za daného množství přidané glukózy je možné, bez rizika překyselení, zastavit kvašení na konci daného časového období, vypočítaného jako funkce času, požadovaného pro dosažení minimálního pH. To umožňuje lepší kontrolu pravidelnosti konečného pH a struktury výrobku na konci kvašení.
Pro uskutečnění způsobu podle vynálezu a v závislosti na stupni okyselení, kterého je žádoucí dosáhnout, činí výhodně množství glukózy přidávané do mléka před kvašením 0,5 až lOg.l 1 a lépe 0,5 až 5 g.l
Kvašený výrobek získaný tímto způsobem může být uchováván po několik hodin pri teplotě blízké teplotě kvašení, bez poklesu pH, což umožňuje odstranit zařízení pro uchovávání meziproduktu v chladu a zvýšit kapacity kvasných tanků.
Uplatňování způsobu podle vynálezu umožňuje snížení dodatečného okyselení v kvašených výrobcích během jejich delší doby uchovávání. Stupeň dodatečného okyselení se může lišit v závislosti na složení zákvasu a na množství použité glukózy. Ovšem dodatečné okyselení je vždy jasně nižší než to, ktereje pozorováno v případě jogurtů, získaných s běžným zákvasem a běžnými způsoby.
Například pokusy, prováděné autory vynálezu, ukázaly, že za stejných podmínek uchovávání (28 dnů uchovávání při 10 °C) je Δ pH (rozdíl mezi pH v den 0, tj. DO a pH v den 28, tj. D28) mezi 0,05 a 0,4 v případě výrobků získaných za použití zákvasu podle vynálezu, zatímco v případě kontrolního zákvasu, kdy je kmen L. bulgaricus podle vynálezu nahražen kmenem divokého typuje Δ pH vždycky větší než 0,7.
Toto slabé dodatečné okyselování je doprovázeno dobrým přežíváním kmenů zahrnutých v zákvasu; populace L. bulgaricus je v kvašeném výrobku získaném podle vynálezu na konci uchovávání pouze mírně menší než v kontrolním výrobku.
Předmětem předkládaného vynálezu jsou také kvašené mléčné výrobky, které mohou být získány prováděním způsobu podle vynálezu.
Tyto výrobky mohou být uchovávány po dlouhou dobu a při vyšších teplotách než výrobky získané za použití běžných metod, ajejich organoleptické vlastnosti zůstávají během uchovávání stálé.
Příklady provedení vynálezu
Příklad 1
Biochemické testování β-galaktosidázové aktivity mutantu podle vynálezu
Aktivitu β-galaktosidázy kmene 1-1968 byla srovnána s toutéž aktivitou u kmene divokého typu L. bulgaricus (dále zde označovaného LbS), od něhož byl odvozen.
Bakterie se kultivují přes noc na MRS agarovém médiu (Merck) pri 37 °C v anaerobní nádobě (Merck) v přítomnosti zprostředkovatele kyslíku (AnaerocultA, Merck).
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Klička bakterií, mající objem 10 μΐ (Nunc), byla resuspendována v 1 ml sterilní vody. Bakterie byly lyžovány 2 cykly důkladného protřepávání, 20 sekund při rychlosti otáčení 5000 otáček za minutu v přítomnosti skleněných perliček (0,5 mm v průměru, BIOSPEC PRODUCTS) a poté přidáním OJ 5 ml chloroformu. Směs byla protřepávána 30 minut při 37 °C a objem byl upraven na 2 ml sterilní vodou při 4 °C. Poté byla měřena aktivita β-galaktosidázy. Reakce byla započata tak, že k 0,2 ml buněčné suspenze bylo přidáno 1,2 ml 0,067 mol.l“1 NaH2PO4 pufru o pH 6,8, poté 0,05 ml L-cysteinu (SIGMA) a v čase t=0 0,05 ml o-nitrofenyl-p-D-galaktopyranosidu (SIGMA). Enzymová reakce byla zastavena po 0, 2, 5 nebo 10 minutách přidáním 1 ml 10% Na2CO3 pufru a po odstředění reakčního média bylo v supematantu prováděno měření OD (optιοί o ké hustoty) při 400 nm.
Galaktosidázové aktivity u LbS rodičovského kmene a u mutantu 1-1968 podle vynálezu, měřené jako funkce času, jsou uvedeny na obr. I.
Tyto výsledky ukazují, že β-galaktosidázaje u mutantu podle vynálezu zcela inaktivní.
Příklad 2
Stálost 1-1968 mutantního kmene L. bulgaricus
Stálost mutantu 1-1968 byla testována v médiu, obsahujícím jako zdroj uhlíku buď směs glukózy a laktózy, nebo pouze laktózu.
Kultura 1-1968, získaná v médiu MRS obsahujícím glukózu, byla pěstována ve vedlejší kultuře na sterilizovaném mléku, doplněném kvasnicovým autolyzátem (2 g/1), která mohla nebo nemusela být doplněna glukózou (20 g/1). Po dosažení pH v hodnotě 5,2 (srážení mléka) byly z každé vedlejší kultury odebrány vzorky, z nichž se určovala schopnost bakterií kvasit cukry a přítomnost β-galaktosidázové aktivity (X-gal deskové stanovení: bílé kolonie = β-galaktosidáza minus;
modré kolonie - β-galaktosidáza plus).
Výsledkyjsou uvedeny níže v Tabulce 1.
Tabulka 1
médium | mléko + glukóza (20 g/1) | mléko |
doba k dosažení pH 5,2 | 6 hodin | 20 hodin |
kvašení cukrů | glukóza, fruktóza, mannóza | laktóza, glukóza, fruktóza, mannóza |
X-gal deskové stanovení | 100 % bílých kolonií | 20 % bílých kolonií 80 % modrých kolonií |
Tyto výsledky ukazují, že v přítomnosti glukózy se kmen 1-1968 nemění na kmen, schopný 40 využívat laktózu. Naproti tomu v médiu, obsahujícím laktózu jako jediný zdroj uhlíku, byl pozorován rychlý zvrat kmene 1-1968 do původního stavu.
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Příklad 3
Okyselování, dodatečné okyselování a podmínky přežití varianty 1-1968 L. bulgaricus v symbió5 ze ze S. thermophilus\ Způsob výroby stabilizovaného jogurtu (kvašení ve větrané sušárně).
Jogurtové zákvasy byly připraveny spojením kmene 1-1968 podle vynálezu s různými průmyslovými kmeny 5. thermophihts (použité kmeny S. thermophihts jsou zde dále nazývány STÍ, ST2 a ST3).
io
Pro srovnání byly zákvasy připraveny také spojením LbS rodičovského kmene a stejných kmenů
5. thernwphilus.
Pro přípravu zákvasů byly kmeny zakvašeny odděleně na 1% na následující směsí:
složení pro 1 litr:
135 g práškového odstředěného mléka 2 g kvasnicového autolyzátu
920 ml destilované vody g glukózy (pouze pro kmen 1-1968) hydratace: 10 minut pasterizace: 30 minut při 95 °C
Mléko bylo poté ochlazeno na 44 °C a zaočkováno a následně inkubováno pri teplotě 44 °C až k dosažení kyselosti 85 °D (Dornicovy stupně) pro streptokoky a 80 °D pro laktobacily.
Kultury pak byly ochlazeny k zisku zákvasu obsahujícího 80% Streptococcus thermvphilus a 20 % Lactobacillus bulgaricus.
Takto připravené zákvasy byly použity k zaoěkování následujícího přípravku:
složení pro 1 litr:
99 % mléka
0, I nebo 2 g/1 glukózy hydratace: 10 minut pasterizace: 10 minut při 95 °C
Mléko pak bylo ochlazeno na 44 °C a zaočkováno na 1%.
Složení zákvasu a množství přidané glukózy je pro každý pokus uvedeno níže v Tabulce II.
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Tabulka II
pokus | glukóza (g/1) | kmeny | procenta |
1 | 0 | ST3 ST2 LbS | 64% 16% 20 % |
2 | 0 | ST3 ST2 1-1968 | 64% 16 % 20 % |
3 | 1 | ST3 ST2 1-1968 | 64 % 16 % 20 % |
1 4 | 0 | STÍ LbS | 80 % 20 % |
5 | 0 | STÍ 1-1968 | 80 % 20 % |
6 | 2 | STÍ 1-1968 | 80 % 20 % |
Po zaočkování bylo mléko umístěno do baněk s kulatým dnem a inkubováno při teplotě 44 °C. Během inkubace byl monitorován profil okyselování. Výrobky byly při pH 4,6 zachovány nesražené ochlazením v chladicí jednotce (16 hodin pri 4 °C), io Poté byly výrobky podrobeny testu uchovávání při 10 °C. V tomto testu byla měřena hodnota pH a Domicova kyselost po l, 14, 21, a 28 dnech uchovávání.
Výsledky okyselování (doba k dosažení pH 4,6 a hodnota pH v Čase 24 hodin) jsou uvedeny níže v Tabulce lil:
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Tabulka IH
pokus | doba k dosažení pH 4,6 (min) | doba k dosažení pH 4,5 (min) | pH v čase 24 hodin |
1 | 215 | 236 | 3,67 |
2 | 550 | 778 | 4,33 |
3 | 416 | 507 | 4,26 |
4 | 225 | 241 | 3,67 |
5 | 660 | > 1500 | 4,54 |
6 | 390 | 465 | 4,35 |
Výsledky testu uchovávání při 10°C (monitorování pH a Domicovy kyselosti) a testu přežití (populace S. thermophilus a L. bulgaricus) po 28 dnech jsou uvedeny níže v Tabulce IV:
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Tabulka IV
pokus | doba skladování (dny) | pH | Dornicova kyselost | S. thermophilus (buftky/ml) | L. bulgaricus (buftky/ml) |
1 | 1 | 4,41 | 101 | 7.25E+08 | 3,35E+08 |
14 | 3,98 | 140 | ND | ND | |
21 | 3,95 | 145 | ND | ND | |
28 | 3,9 | 148 | 7,35E+08 | 3,30E+O8 | |
2 | 1 | 4,5 | 93 | 5,60E+08 | 2,90E+07 |
14 | 4,23 | 110 | ND | ND | |
21 | 4,18 | 112 | ND | ND | |
28 | 4,19 | 114 | 5,65E+08 | 1,87E+O7 | |
3 | 1 | 4,49 | 96 | 6,90E+08 | 7,45E+07 |
14 | 4,14 | 115 | ND | ND | |
21 | 4,15 | 117 | ND | ND | |
28 | 4,15 | 120 | 8,65E+08 | 6,3OE+07 | |
4 | l | 4,39 | 105 | 6,30E+07 | 4,40E+08 |
14 | 3,91 | 145 | ND | ND | |
21 | 3,9 | 151 | ND | ND | |
28 | 3,85 | 157 | 4.70E+08 | 6,30E+08 | |
5 | 1 | 4,6 | 85 | 9,05E+08 | 6,70E+07 |
14 | 4,58 | 80 | ND | ND | |
21 | 4,53 | 80 | ND | ND | |
28 | 4,61 | 79 | 9.40E+08 | 7,0OE+O7 | |
6 | 1 | 4,51 | 89 | l,05E+09 | l,96E+08 |
14 | 4,38 | 90 | ND | ND | |
21 | 4,39 | 96 | ND | ND | |
28 | 4,42 | 90 | l,62E+09 | l,91E+08 |
ND = nestanoveno
Tyto výsledky ukazují, že jogurty, vyráběné za použití symbiózy, spojující kmen 1-1968 s jedním nebo dvěma kmeny 5. thermophilus, vykazují výrazně snížené dodatečné okyselování vzhledem ke stejné symbióze s rodičovským kmenem LbS, a současně uchovávají bohatou populaci až do io konce kvašení a dobré přežívání po 28 dní při 10 °C.
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Zastavení okyseIování a udržování pH kolem 4,6 až 4,5 po alespoň 24 hodin pří 44 °C umožňuje, v kontextu výroby míchaného jogurtu, snížit nebo dokonce odstranit běžně používanou fázi ochlazování v tanku.
SEZNAM SEKVENCÍ io <1 IO> COMPAGNIE GERVAIS DANONE GENDRE, Fran9ois BENBAD1S, Laurent BR1GNON, Pierre <120> MUTANTNÍ KMENY LACTOBACILLUS BULGARICUS POSTRÁDAJÍCÍ β-GALAKTOSlDÁZOVOU AKTIVITU <130> MJPcbl9l/l43 <140>
<14l>
<150> FR9806456 <151> 1998-05-22 <160> 3 < 170> Patentln Ver. 2.1 <210> 1 <21I> 5059 <212> DNA <213> Lactobacillus bulgaricus <220>
<221> CDS <222> (122)..(1873) <220>
<221> CDS <222> (1877)..(4519) <400> I gcttgtctca cgcttgtcgt acgcggccgg tgcctttggc aacgacgtct tctacgcgac 60 tctgtcaacc tactttatcg tcttcgtcac cacccacctc tttaatgccg gtgaccacaa 120 g atg atc ttt atc atc acc aac ttg atc acc gcc atc cgg atc ggg gaa 169 Met Ile Phe Ile Ile Thr Asn Leu Ile Thr Ala Ile Arg Ile Gly Glu
10 15
gtc Val | ctg ctc gac ccc | ttg atc ggt aac gcc atc gac cgg acc gaa agc | ||||||||||||
Leu Leu Asp 20 | Pro | Leu | Ile Gly Asn 25 | Ala | Ile | Asp Arg | Thr 30 | Glu Ser | ||||||
cgg | tgg | ggg | aag | ttc | aag | ccc | tgg | gtt | gtg | ggc | ggg ggg | atc | atc | agc |
Arg | Trp | Gly | Lys | Phe | Lys | Pro | Trp | Val | Val | Gly Gly Gly | Ile | Ile | Ser | |
35 | 40 | 45 |
tca tta gcc | ctc tta gcc | ctc Leu 55 | ttt acc gac ttt ggc ggc att | aac caa Asn Gin | 313 | |||||||||||
Ser Leu 50 | Ala | Leu Leu | Ala | Phe | Thr | Asp Phe | Gly 60 | Gly | Ile | |||||||
agc | aac | ccc | gtt | gtt | tac | tta | gta | atc | ttc | ggt | att | gtt | tac | ttg | att | 361 |
Ser | Asn | Pro | Val | Val | Tyr | Leu | Val | Ile | Phe | Gly | Ile | Val | Tyr | Leu | Ile | |
65 | 70 | 75 | 80 | |||||||||||||
atg | gat | atc | ttc | tac | tca | ttt | aaa | gac | act | ggc | ttc | tgg | gcc | atg | atc | 409 |
Met | Asp | Ile | Phe | Tyr | Ser | Phe | Lys | Asp | Thr | Gly | Phe | Trp | Ala | Met | Ile | |
85 | 90 | 95 | ||||||||||||||
ccg | gcc | ttg | tcc | ctg | gat | tcc | cgg | gaa | aga | gag | aag | acc | tcc | acc | ttc | 457 |
Pro | Ala | Leu | Ser | Leu | Asp | Ser | Arg | Glu | Arg | Glu | Lys | Thr | Ser | Thr | Phe | |
100 | 105 | 110 | ||||||||||||||
gcc | aga | gtc | ggc | tcc | acc | atc | ggg | gcc | aac | ctg | gtc | ggg | gta | gtc | atc | 505 |
Ala | Arg | Val | Gly | Ser | Thr | Ile | Gly | Ala | Asn | Leu | Val | Gly | Val | Val | Ile |
115 120 125
acc cca atc atc | ctc ttc | ttc tcg gcc agc aag gcc aac ccc aac ggg | 553 | |||||||||||||
Thr Pro 130 | Ile | Ile | Leu | Phe | Phe Ser 135 | Ala Ser | Lys | Ala Asn Pro 140 | Asn Gly | |||||||
gat | aag | cag | ggc | tgg | ttc | ttc | ttt | gcc | ttg | atc | gtg | gcc | att | gtc | ggc | 601 |
Asp | Lys | Gin | Gly | Trp | Phe | Phe | Phe | Ala | Leu | Ile | Val | Ala | Ile | Val | Gly | |
145 | 150 | 155 | 160 | |||||||||||||
atc | ttg | acc | tca | att | acc | gtt | ggt | ctt | ggt | .act | cac | gaa | gta | aaa | tcc | 649 |
Ile | Leu | Thr | Ser | Ile | Thr | Val | Gly | Leu | Gly | Thr | His | Glu | Val | Lys | Ser | |
165 | 170 | 175 | ||||||||||||||
gcc | ctg | cgg | gaa | agc | aat | gaa | aag | acc | act | ttg | aag | cag | gtc | ttt | aag | 697 |
Ala | Leu | Arg | Glu | Ser | Asn | Glu | Lys | Thr | Thr | Leu | Lys | Gin | Val | Phe | Lys | |
180 | 185 | 190 | ||||||||||||||
gtc | ctg | ggg | caa | aac | gac | cag | ctc | ctc | tgg | ctg | gcc | ttt | gcc | tac | tgg | 745 |
Val | Leu | Gly | Gin | Asn | Asp | Gin | Leu | Leu | Trp | Leu | Ala | Phe | Ala | Tyr | Trp | |
195 | 200 | 205 | ||||||||||||||
ttt | tac | ggc | ctg | ggt | atc | aac | acc | ctg | aac | gct | .ctg | caa | ctt | tac | tac | 793 |
Phe | Tyr | Gly | Leu | Gly | Ile | Asn | Thr | Leu | Α3Π | Ala | Leu | Gin | Leu | Tyr | Tyr | |
210 | 215 | 220 | ||||||||||||||
ttc | tca | tac | atc | tta | ggc | gat | gcc | cgc | ggc | tac | agc | ctg | ctt | tac | acc | 841 |
Phe | Ser | Tyr | Ile | Leu | Gly Asp | Ala | Arg | Gly | Tyr | Ser | Leu | Leu | Tyr | Thr | ||
225 | 230 | 235 | 240 | |||||||||||||
atc | aac | acc | ttt | gtc | ggt | tta | atc | tet | gca | tcc | ttc | ttc | cca | tca | ctg | 889 |
ne | Asn | Thr | Phe | Val | Gly | Leu | Ile | Ser | Ala | Ser | Phe | Phe | Pro | Ser | Leu | |
245 | 250 | 255 | ||||||||||||||
gcc | aag | aag | ttc | aac | aga | aat | cgc | ctc | ttc | tac | gcc | tgc | atc | gcg | gtg | 937 |
Ala | Lys | Lys | Phe | Asn | Arg | Asn | Arg | Leu | Phe | Tyr | Ala | Cys | Ile | Ala | val | |
260 | 265 | 270 | ||||||||||||||
atg | ctg | tta | ggg | atc | ggg | gtc | ttc | tcc | gtg | gcc | agc | ggt | tet | ctg | gcc | 985 |
Met | Leu | Leu | Gly | Ile | Gly | Val | Phe | Ser | Val | Ala | Ser | Gly | Ser | Leu | Ala | |
275 | 280 | 285 | ||||||||||||||
ctg | tcc | ctt | gtt | ggg | gca | gaa | ttc | ttc | ttt | att | ccg | cag | cct | ctg | gcc | 1033 |
Leu | Ser | Leu | Val | Gly | Ala | Glu | Phe | Phe | Phe | Ile | Pro | Gin | Pro | Leu | Ala | |
290 | 295 | 300 | ||||||||||||||
ttc | ctg | gtc | gtt | ttg | atg | atc | atc | tet | gac | gct | gtt | gaa | tac | ggc | cag | 1081 |
Phe | Leu | Val | Val | Leu | Met | Ile | Ile | Ser | Asp | Ala | Val | Glu | Tyr | Gly | Gin | |
305 | 310 | 315 | 320 | |||||||||||||
ctg | aaa | act | ggc | cac | aga | gac | gaa | gct | ttg | acc | ctg | tet | gtc | cgg | cca | 1129 |
Leu | Lys | Thr | Gly | His | Arg | Asp | Glu | Ala | Leu | Thr | Leu | Ser | Val | Arg | Pro |
325 330 335
-11CZ 302175 B6
ttg Leu | gtc Val | gat Asp | aag Lys 340 | ctg Leu | ggc ggg gcc Gly Gly Ala | ttg Leu 345 | tcc Ser | aac Asn | tgg Trp | ttt Phe | gtt Val 350 | tcc Ser | ttg Leu | 1177 |
att | gcc | tta | act | gcc | ggc atg acc | act | ggg | gcg | act | gcc | tea | aca | att | 1225 |
Ile | Ala | Leu | Thr | Ala | Gly Met Thr | Thr | Gly | Ala | Thr | Ala | Ser | Thr | Ile | |
355 | 360 | 365 | ||||||||||||
aca | get | cat | ggc | cag | atg gtc ttc | aag | tta | get | atg | ttt | gcc | tta | ccg | 1273 |
Thr | Ala | His | Gly | Gin | Met Val Phe | Lys | Leu | Ala | Met | Phe | Ala | Leu | Pro | |
370 | 375 | 380 | ||||||||||||
gca | gtc | atg | ctc | ttg | atc get gtt | tet | att | ttc | gcc | aaa | aag | gtc | ttc | 1321 |
Ala | Val | Met | Leu | Leu | Ile Ala Val | Ser | Ile | Phe | Ala | Lys | Lys | Val | Phe | |
385 | 390 | 395 | 400 | |||||||||||
ttg | act | gaa | gaa | aag | cac gcg gaa | atc | gtc | gac | cag | ctg | gaa | act | caa | l3ťÝ |
Leu | Thr | Glu | Glu | Lys | His Ala Glu | Ile | Val | Asp | Gin | Leu | Glu | Thr | Gin | |
405 | 410 | 415 | ||||||||||||
ttc | age | caa | age | cat | gcc caa aag | ccg | gcg | caa | get | gaa | age | ttc | act | 1417 |
Phe | Ser | Gin | Ser | His | Ala Gin Lys | Pro | Ala | Gin | Ala | Glu | Ser | Phe | Thr | |
420 | 425 | 430 | ||||||||||||
ttg | gcc | age | cca | gtc | tcc gga caa | tta | atg | aac | ctg | gac | atg | gtt | gac | 1465 |
Leu | Ala | Ser | Pro | Val | Ser Gly Gin | Leu | Met | Asn | Leu | Asp | Met | Val | Asp | |
435 | 440 | 445 | ||||||||||||
gac | ccg | gtc | ttt | gcc | gac aaa aag | tta | ggc | gac | ggc | ttt | gcc | ctg | gtg | 1513 |
Asp | Pro | Val | Phe | Ala | Asp Lys Lys | Leu | Gly | Asp | Gly | Phe | Ala | Leu | Val | |
450 | 455 | 4 60 | ||||||||||||
cca | gca | gac | ggt | aag | gtc tac gcg | cca | ttt | gcc | ggt | act | gtc | ege | cag | 1561 |
Pro | Ala | Asp | Gly | Lys | Val Tyr Ala | Pro | Phe | Ala | Gly | Thr | Val | Arg | Gin | |
465 | 470 | 475 | 480 | |||||||||||
ctg | gcc | aag | acc | cgg | cac tcg atc | gtc | ctg | gaa | aat | gaa | cat | ggg | gtc | 1609 |
Leu | Ala | Lys | Thr | Arg | His Ser Ile | Val | Leu | Glu | Asn | Glu | His | Gly | Val | |
485 | 490 | 495 | ||||||||||||
ttg | gtc | ttg | att | cac | ctt ggc ctg | ggc | acg | gtc | aaa | tta | aac | ggg | act | 1657 |
Leu | Val | Leu | Ile | His | Leu Gly Leu | Gly | Thr | Val | Lys | Leu | Asn | Gly | Thr | |
500 | 505 | 510 | ||||||||||||
ggc | ttt | gtc | age | tat | gtt gaa gag | ggc | age | cag | gta | gaa | gcc | ggc | cag | 1705 |
Gly | Phe | Val | Ser | Tyr | Val Glu Glu | Gly | Ser | Gin | Val | Glu | Ala | Gly | Gin | |
515 | 520 | 525 | ||||||||||||
cag | atc | ctg | gaa | ttc | tgg gac ccg | gcg | atc | aag | cag | gcc | aag | ctg | gac | 1753 |
Gin | Ile | Leu | Glu | Phe | Trp Asp Pro | Ala | Ile | Lys | Gin | Ala | Lys | Leu | Asp | |
530 | 535 | 540 | ||||||||||||
gac | acg | gta | atc | gtg | acc gtc atc | aac | age | gaa | act | ttc | gca | aat | age | 1801 |
Asp | Thr | Val | Ile | Val | Thr Val Ile | Asn | Ser | Glu | Thr | Phe | Ala | Asn | Ser | |
545 | 550 | 555 | 560 | |||||||||||
cag | atg | ctc | ttg | ccg | atc ggc cac | age | gtc | caa | gcc | ctg | gat | gat | gta | 1849 |
Gin | Met | Leu | Leu | Pro | Ile Gly His | Ser | Val | Gin | Ala | Leu | Asp | Asp | Val | |
S65 | 570 | 575 | ||||||||||||
ttc | aag | tta | gaa | ggg | aag aat tag | aaa | atg | age | aat | aag | tta | gta | aaa | 1897 |
Phe | Lys | Leu | Glu | Gly | Lys Asn | Met | Ser | Asn | Lys | Leu | Val | Lys | ||
580 | 585 | 590 | ||||||||||||
gaa | aaa | aga | gtt | gac | cag gca gac | ttg | gcc | tgg | ctg | act | gac | ccg | gaa | 1945 |
Glu | Lys | Arg | Val | Asp | Gin Ala Asp | Leu | Ala | Trp | Leu | Thr | Asp | Pro | Glu | |
595 | 600 | 605 | ||||||||||||
gtt | tac | gaa | gtc | aat | aca att ccc | ccg | cac | tcc | gac | cat | gag | tcc | ttc | 1993 |
Val | Tyr | Glu | Val | Asn | Thr Ile Pro | Pro | His | Ser | Asp | His | Glu | Ser | Phe | |
610 | 615 | 620 |
- 12 CZ 302175 B6
caa agc Gin Ser 625 | cag Gin | gaa Glu | gaa Glu | ctg gag gag ggc | aag tcc agt tta gtg cag tcc | 2041 | ||||||||||
Leu Glu 630 | Glu | Gly | Lys | Ser Ser Leu Val 635 | Gin | Ser | ||||||||||
ctg | gac | ggg | gac | tgg | ctg | att | gac | tac | gct | gaa | aac | ggc | cag | gga | cca | 2089 |
Leu | Asp | Gly | Asp | Trp | Leu | Ile | Asp | Tyr | Ala | Glu | Asn | Gly | Gin | Gly | Pro | |
640 | 645 | 650 | 655 | |||||||||||||
gtc | aac | ttc | tat | gca | gaa | gac | ttt | gac | gat | agc | aat | ttt | aag | tca | gtc | 2137 |
Val | Asn | Phe | Tyr | Ala | Glu | Asp | Phe | Asp | Asp | Ser | Asn | Phe | Lys | Ser | Val | |
660 | 665 | 670 | ||||||||||||||
aaa | gta | ccc | ggc | aac | ctg | gaa | ctg | caa | ggc | ttt | ggc | cag | ccc | cag | tat | 2185 |
Lys | Val | Pro | Gly | Asn | Leu | Glu | Leu | Gin | Gly | Phe | Gly | Gin | Pro | Gin | Tyr | |
675 | 680 | 685 | ||||||||||||||
gtc | aac | gtc | caa | tat | cca | tgg | gac | ggc | agt | gag | gag | att | ttc | ccg | ccc | 2233 |
Val | Asn | Val | Gin | Tyr | Pro | Trp | Asp | Gly | Ser | Glu | Glu | Ile | Phe | Pro | Pro | |
690 | 695 | 700 | ||||||||||||||
caa | att | cca | agc | aaa | aat | ccg | ctc | gct | tet | tat | gtc | aga | tac | ttt | gac | 2281 |
Gin | Ile | Pro | Ser | Lys | Asn | Pro | Leu | Ala | Ser | Tyr | Val | Arg | Tyr | Phe | Asp | |
705 | 710 | 715 | ||||||||||||||
ctg | gat | gaa | gct | ttc | tgg | gac | aag | gaa | gtc | agc | ttg | aag | ttt | gac | ggg | 2329 |
Leu | Asp | Glu | Ala | Phe | Trp | Asp | Lys | Glu | Val | Ser | Leu | Lys | Phe | Asp | Gly | |
720 | 725 | 730 | 735 | |||||||||||||
gcg | gca | aca | gcc | atc | tat | gtc | tgg | ctg | aac | ggc | cac | ttc | gtc | ggc | tac | 2377 |
Ala | Ala | Thr | Ala | Ile | Tyr | Val | Trp | Leu | Asn | Gly | His | Phe | Val | Gly | Tyr | |
740 | 745 | 750 | ||||||||||||||
ggg | gaa | gac | tcc | ttt | acc | cca | agc | gag | ttt | atg | gtt | acc | aag | ttc | ctc | 2425 |
Gly | Glu | Asp | Ser | Phe | Thr | Pro | Ser | Glu | Phe | Met | Val | Thr | Lys | Phe | Leu | |
755 | 760 | 765 | ||||||||||||||
aag | aaa | gaa | aat | aac | cgc | ctg | gca | gtg | gct | ctc | tac | aag | tat | tet | tcc | 2473 |
Lys | Lys | Glu | Asn | Asn | Arg | Leu | Ala | Val | Ala | Leu | Tyr | Lys | Tyr | Ser | Ser | |
770 | 775 | 780 | ||||||||||||||
gcc | tcc | tgg | ctg | gaa | gac | cag | gac | ttc | tgg | cgc | atg | tet | ggt | ttg | ttc | 2521 |
Ala | Ser | Trp | Leu | Glu | Asp | Gin | Asp | Phe | Trp | Arg | Met | Ser | Gly | Leu | Phe | |
785 | 790 | 795 | ||||||||||||||
aga | tca | gtg | act | ctt | cag | gcc | aag | ccg | cgt | ctg | cac | ttg | gag | gac | ctt | 2569 |
Arg | Ser | Val | Thr | Leu | Gin | Ala | Lys | Pro | Arg | Leu | His | Leu | Glu | Asp | Leu | |
800 | 805 | 810 | 815 | |||||||||||||
aag | ctt | acg | gcc | agc | ttg | acc | gat | aac | tac | caa | aaa | gga | aag | ctg | gaa | 2617 |
Lys | Leu | Thr | Ala | Ser | Leu | Thr | Asp | Asn | Tyr | Gin | Lys | Gly | Lys | Leu | Glu | |
820 | 825 | 830 | ||||||||||||||
gtc | gaa | gcc | aat | att | gcc | tac | cgc | ttg | cca | aat | gcc | agc | ttt | aag | ctg | 2665 |
val | Glu | Ala | Asn | Ile | Ala | Tyr | Arg | Leu | Pro | Asn | Ala | Ser | Phe | Lys | Leu | |
835 | 840 | 845 | ||||||||||||||
gaa | gtg | cgg | gat | agt | gaa | ggt | gac | ttg | gtt | gct | gaa | aag | ctg | ggc | cca | 2713 |
Glu | Val | Arg | Asp | Ser | Glu | Gly | Asp | Leu | Val | Ala | Glu | Lys | Leu | Gly | Pro | |
850 | 855 | 860 | ||||||||||||||
atc | aga | agc | gag | cag | ctg | gaa | ttc | act | ctg | gct | gat | ttg | cca | gta | gct | 2761 |
Ile | Arg | Ser | Glu | Gin | Leu | Glu | Phe | Thr | Leu | Ala | Asp | Leu | Pro | Val | Ala | |
865 | 870 | 875 | ||||||||||||||
gcc | tgg | agc | gcg | gaa | aag | cct | aac | ctt | tac | cag | gtc | cgc | ctg | tat | tta | 2809 |
Ala | Trp | Ser | Ala | Glu | Lys | Pro | Asn | Leu | Tyr | Gin | Val | Arg | Leu | Tyr | Leu | |
880 | 885 | 890 | 895 |
- 13 CZ 302175 B6
tac Tyr | cag gca ggc | age Ser 900 | ctc tta gag gtt | age cgg cag gaa gtg ggt | ttc Phe | |||||||||
Gin Ala | Gly | Leu | Leu | Glu | Val | Ser 905 | Arg | Gin | Glu | Val | Gly 910 | |||
cgc | aac ttt | gaa | cta | aaa | gac | ggg | att | atg | tac | ctt | aac | ggc | cag | cgg |
Arg | Asn Phe | Glu 915 | Leu | Lys | Asp | Gly | Ile 920 | Met | Tyr | Leu | Asn | Gly 925 | Gin | Arg |
atc | gtc ttc | aag | ggg | gcc | aac | cgg | cac | gaa | ttt | gac | agt | aag | ttg | ggc |
Ile | Val Phe 930 | Lys | Gly | Ala | Asn | Arg 935 | His | Glu | Phe | Asp | Ser 940 | Lys | Leu | Gly |
cgg | get atc | aca | gaa | gag | gat | atg | atc | tgg | gat | atc | aag | acc | atg | aag |
Arg | Ala Ile 945 | Thr | Glu | Glu | Asp 950 | Met | Ile | Trp | Asp | Ile 955 | Lys | Thr | Met | Lys |
ega | age aac | atc | aat | get | gtc | cgc | tgc | tet | cac | tac | ccg | aac | cag- tcc | |
Arg 960 | Ser Asn | Ile | Asn | Ala 965 | Val | Arg | Cys | Ser | His 970 | Tyr | Pro | Asn | Gin | Ser 975 |
ctc | ttt tac | cgg | ctc | tgt | gac | aag | tac | ggc | ctt | tac | gtc | att | gat | gaa |
Leu | Phe Tyr | Arg | Leu 980 | Cys | Asp | Lys | Tyr | Gly 985 | Leu | Tyr | Val | Ile | Asp 990 | Glu |
get | aac ctg | gaa | age | cac | ggc | acc | tgg | gaa | aaa | gtg | ggg | ggg | cac | gaa |
Ala | Asn Leu | Glu 995 | Ser | His | Gly | Thr | Trp L000 | Glu | Lys | Val | Gly | Gly 1005 | His | Glu |
gat | cct age | ttc | aat | gtt | cca | ggc | gat | gac | cag | cat | tgg | ctg | gga | gcc |
Asp | Pro Ser 1010 | Phe | Asn | Val | Pro | Gly 1015 | Asp | Asp | Gin | His | Trp 1020 | Leu | Gly | Ala |
age | tta tcc | cgg | gtg | aag | aac | atg | atg | get | cgg | gac | aag | aac | cat | get |
Ser j | Leu Ser .025 | Arg | Val | Lys | Asn L030 | Met | Met | Ala | Arg | Asp 1035 | Lys | Asn | His | Ala |
tea | atc ctg | atc | tgg | tet | tta | ggc | aat | gag | tet | tac | gcc | ggc | act | gtc |
Ser Ile Leu 1040 | Ile | Trp Ser 1045 | Leu | Gly | Asn | Glu Ser 1050 | Tyr | Ala | Gly | Thr | Val 1055 | |||
ttt | gcc caa | atg | get | gat | tac | gtc | cgg | aag | get | gat | ccg | acc | cgg | gtt |
Phe | Ala Gin | Met Ala 1060 | Asp | Tyr | Val | Arg | Lys L065 | Ala | Asp | Pro | Thr Arg 1070 | Val | ||
cag | cac tat | gaa | ggg | gtg | acc | cac | aac | cgg | aag | ttt | gac | gac | gcc | acc |
Gin | His Tyr | Glu L075 | Gly | val | Thr | His | Asn 1080 | Arg | Lys | Phe | Asp | Asp 1085 | Ala | Thr |
cag | att gaa | age | cgg | atg | tat | get | ccg | gce | aag | gta | att | gaa | gaa | tac |
Gin | Ile Glu 1090 | Ser | Arg | Met | Tyr | Ala 1095 | Pro | Ala | Lys | Val | Ile 1100 | Glu | Glu | Tyr |
ttg | acc aat | aaa | cca | gcc | aag | cca | ttt | atc | tea | gtt | gaa | tac | get | cac |
Leu | Thr Asn | Lys | Pro | Ala | Lys | Pro | Phe | Ile | Ser | Val | Glu | Tyr | Ala | His |
1105 1110 1115
gcc | atg | ggc | aac | tcc | gtc | ggt |
Ala | Met | Gly | Asn | Ser | Val | Gly |
1120 | 1125 | |||||
aaa | tac | ccc | cac | tac | cag | ggc |
Lys | Tyr | Pro | His | Tyr | Gin | Gly |
1140
gga | ctg | gaa aaa | gac | ggg | cac |
Gly | Leu | Glu Lys 1155 | Asp | Gly | His |
gac ctg gcc gcc tac acg gcc ctg gaa Asp Leu Ala Ala Tyr Thr Ala Leu Glu 1130 1135 ggc ttc atc Gly Phe Ile 1145 ctg ctt tat Leu Leu Tyr 1160
2357
2905
2953
3001
304-9
3097
3145
3193
3241
3289
3337
3385
3433
3481
3529 tgg gac tgg att gac caa 3577 Trp Asp Trp Ile Asp Gin 1150 ggg ggc gac ttc gat gac 3625 Gly Gly Asp Phe Asp Asp 1165
- 14CZ 302175 B6
cgg Arg | cca acc Pro Thr 1170 | gac Asp | tat Tyr | gaa Glu | ttc tgc Phe Cys 1175 | ggg Gly | aac Asn | ggc Gly | ctg gtc Leu Val 1180 | ttt Phe | gct Ala | gac Asp | 3673 |
cgg | act gaa | tcg | ccg | aaa | ctg gct | aat | gtc | aag | gcc ctt | tac | gcc | aac | 3721 |
Arg | Thr Glu | Ser | Pro | Lys | Leu Ala | Asn | Val | Lys | Ala Leu | Tyr | Ala | Asn | |
1185 | 1190 | 1195 | |||||||||||
ctt | aag tta | gaa | gta | aaa | gat ggg | cag | ctc | ttc | ctc aaa | aac | gac | aat | 3769 |
Leu | Lys Leu | Glu | Val | Lys | Asp Gly | Gin | Leu | Phe | Leu Lys | Asn | Asp | Asn | |
1200 | 1205 | 1210 | 1215 | ||||||||||
tta | ttt acc | aac | agc | tca | tet tac | tac | ttc | ttg | act agt | ctt | ttg | gtc | 3817 |
Leu | Phe Thr | Asn | Ser | Ser | Ser Tyr | Tyr | Phe | Leu | Thr Ser | Leu | Leu | Val | |
1220 | 1225 | 1230 | |||||||||||
gat | ggc aag | ttg | acc | tac | cag agc | cgg | cct | ctg | acc ttt | ggc | ctg | gag | 3865 |
Asp | Gly Lys | Leu | Thr | Tyr | Gin Ser | Arg | Pro | Leu | Thr Phe | Gly | Leu | Glu | |
1235 | 1240 | 1245 | |||||||||||
cct | ggc gaa | tcc | ggg | acc | ttt gcc | ctg | cct | tgg | ccg gaa | gtc | gct | gat | 3913 |
Pro | Gly Glu | Ser | Gly | Thr | Phe Ala | Leu | Pro | Trp | Pro Glu | val | Ala | Asp | |
1250 | 1255 | 1260 | |||||||||||
gaa | aaa gga | gag | gtc | gtc | tac cgg | gta | a cg | gcc | cac tta | aaa | gaa | gac | 3961 |
Glu | Lys Gly | Glu | Val | Val | Tyr Arg | Val | Thr | Ala | His Leu | Lys | Glu | Asp | |
1265 | 1270 | 1275 | |||||||||||
ttg | cct tgg | gcg | gat | gag | ggc ttc | act | gtg | gct | gaa gca | gaa | gaa | gta | 4009 |
Leu | Pro Trp | Ala | Asp | Glu | Gly Phe | Thr | Val | Ala | Glu Ala | Glu | Glu | Val | |
1280 | 1285 | 1290 | 1295 | ||||||||||
gct | caa aag | ctg | ccg | gaa | ttt aag | ccg | gaa | ggg | cgg cca | gat | tta | gtt | 4057 |
Ala | Gin Lys | Leu | Pro | Glu | Phe Lys | Pro | Glu | Gly Arg Pro | Asp | Leu | Val | ||
1300 | 1305 | 1310 | |||||||||||
gat | tcc gac | tac | aac | cta | ggc ctg | aaa | gga | aat | aac ttc | caa | att | ctc | 4105 |
Asp | Ser Asp | Tyr | Asn | Leu | Gly Leu | Lys | Gly | Asn | Asn Phe | Gin | Ile | Leu | |
1315 | 1320 | 1325 | |||||||||||
ttc | tcc aag | gtc | aag | ggc | tgg ccg | gtt | tcc | ctc | aag tat | gcc | ggt | agg | 4153 |
Phe | Ser Lys | Val | Lys | Gly | Trp Pro | Val | Ser | Leu | Lys Tyr | Ala | Gly | Arg | |
1330 | 1335 | 1340 | |||||||||||
gaa | tac ttg | aag | cgg | ctg | ccg gaa | ttt | acc | ttc | tgg cgg | gcc | ctg | acg | 4201 |
Glu | Tyr Leu | Lys | Arg | Leu | Pro Glu | Phe | Thr | Phe | Trp Arg | Ala | Leu | Thr | |
1345 | 1350 | 1355 | |||||||||||
gac | aac gac | cgg | gga | gct | ggt tac | ggc | tat | gat | ctg gcc | cgg | tgg | gaa | 4249 |
Asp | Asn Asp | Arg | Gly | Ala | Gly Tyr | Gly | Tyr | Asp | Leu Ala | Arg | Trp | Glu | |
1360 | 1365 | 1370 | 1375 | ||||||||||
aat | gcc ggc | aag | tat | gcc | ege ttg | aaa | gac | atc | agc tgc | gag | gtc | aag | 4297 |
Asn | Ala Gly | Lys | Tyr | Ala | Arg Leu | Lys | Asp | Ile | Ser Cys | Glu | Val | Lys | |
1380 | 1385 | 1390 | |||||||||||
gaa | gac tcc | gtt | ttg | gtc | aag act | gcc | ttt | acg | ttg cct | gtc | gcc | tta | 4345 |
Glu | Asp Ser | Val | Leu | Val | Lys Thr | Ala | Phe | Thr | Leu Pro | Val | Ala | Leu | |
1395 | 1400 | 1405 | |||||||||||
aag | ggt gat | tta | act | gtg | acc tat | gaa | gtc | gat | gga cgg | ggc | aag | att | 4393 |
Lys | Gly Asp | Leu | Thr | Val | Thr Tyr | Glu | Val | Asp | Gly Arg | Gly | Lys | Ile | |
1410 | 1415 | 1420 | |||||||||||
gct | gta aca | gct | gac | ttc | cca ggc | gcg | gaa | gaa | gcc ggt | ctc | ttg | cca | 4441 |
Ala | Val Thr | Ala | Asp | Phe | Pro Gly | Ala | Glu | Glu | Ala Gly | Leu | Leu | Pro |
1425 1430 1435
- 15CZ 302175 B6
gcc Ala 1440 | ttt Phe 1 | ggc ttg Gly Leu | aac ctg gcc | ctg cca | aaa Lys | gaa Glu 1450 | ctg Leu | acc gat | tac cgc Tyr Arg 1455 | 4489 | |||||
Asn Leu 1445 | Ala | Leu | Pro | Thr | Asp | ||||||||||
tac | tat | ggt | ctg | gga | cct | aat | gag | agc | taa | ccagaccgct | tggaaggtaa | 4539 | |||
Tyr | Tyr | Gly | Leu | Gly | Pro | Asn | Glu | Ser |
1460 1465 ttacctgggc atctaccagg gagcggtaaa aaagaacttt agcccatacc tgcgtccgca 4599 ggaaacgggc aaccggagca aggttcgctg gtaccagctc tttgatgaaa agggcggctt 4659 ggaatttacg gccaatgggg cagacttgaa cttgtctgct ttgccatatt ctgccgccca 4719 aattgaagca gcggaccacg cttttgaact gactaacaat tacacttggg ttagagcctt 4779 aagcgcccag atgggggtcg gcggggatga ctcctggggg cagaaggtcc acccggaatt 4939 ctgcctggat gctcaaaaag cccgccagct ccgcctggtg attcagcccc ttttactaaa 4899 ataaatgcta caattgactt aacaggatga aattttagta aaagcaaagc gegtgaggaa 4959 gatggcaacg atcagagaag tgccaaggca gccggcgtgt cgctagcgac ggtttcccgc 5019 gtcttgaact atgaccagac cctgtcagtc aatgaggcaa 5059 <210> 2 <211> 583 <2J2> PRT <213> Lactobacillus bulgaricus <400> 2
Met 1 | Ile Phe | Ile | Ile 5 | Thr Asn Leu | Ile Thr 10 | Ala Ile Arg Ile | Gly 15 | Glu | |||||||
Val | Leu | Leu | Asp | Pro | Leu | Ile | Gly | Asn | Ala | Ile | Asp | Arg | Thr | Glu | Ser |
20 | 25 | 30 | |||||||||||||
Arg | Trp | Gly | Lys | Phe | Lys | Pro | Trp | Val | Val | Gly | Gly | Gly | Ile | Ile | Ser |
35 | 40 | 45 | |||||||||||||
Ser | Leu | Ala | Leu | Leu | Ala | Leu | Phe | Thr | Asp | Phe | Gly | Gly | Ile | Asn | Gin |
50 | 55 | 60 | |||||||||||||
Ser | Asn | Pro | Val | Val | Tyr | Leu | Val | Ile | Phe | Gly | Ile | Val | Tyr | Leu | Ile |
65 | 70 | 75 | 80 | ||||||||||||
Met | Asp | Ile | Phe | Tyr | Ser | Phe | Lys | Asp | Thr | Gly | Phe | Trp | Ala | Met | Ile |
85 | 90 | 95 | |||||||||||||
Pro | Ala | Leu | Ser | Leu | Asp | Ser | Arg | Glu | Arg | Glu | Lys | Thr | Ser | Thr | Phe |
100 | 105 | 110 | |||||||||||||
Ala | Arg | Val | Gly | Ser | Thr | Ile | Gly | Ala | Asn | Leu | Val | Gly | Val | Val | Ile |
115 | 120 | 125 | |||||||||||||
Thr | Pro | Ile | Ile | Leu | Phe | Phe | Ser | Ala | Ser | Lys | Ala | Asn | Pro | Asn | Gly |
130 | 135 | 140 | |||||||||||||
Asp | Lys | Gin | Gly | Trp | Phe | Phe | Phe | Ala | Leu | Ile | Val | Ala | Ile | Val | Gly |
145 | 150 | 155 | 160 |
- 16CZ 302175 B6
lle | Leu | Thr Ser lle Thr Val Gly Leu Gly Thr His Glu Val Lys Ser | |||||||||||||
165 | 170 | 175 | |||||||||||||
Ala | Leu | Arg | Glu | Ser | Asn | Glu | Lys | Thr | Thr | Leu | Lys | Gin | Val | Phe | Lys |
180 | 185 | 190 | |||||||||||||
Val | Leu | Gly | Gin | Asn | Asp | Gin | Leu | Leu | Trp | Leu | Ala | Phe | Ala | Tyr | Trp |
195 | 200 | 205 | |||||||||||||
Phe | Tyr | Gly | Leu | Gly | lle | Asn | Thr | Leu | Asn | Ala | Leu | Gin | Leu | Tyr | Tyr |
210 | 215 | 220 | |||||||||||||
Phe | Ser | Tyr | Xle | Leu | Gly | Asp | Ala | Arg | Gly | Tyr | Ser | Leu | Leu | Tyr | Thr |
225 | 230 | 235 | 240 | ||||||||||||
lle | Asn | Thr | Phe | Val | Gly | Leu | Xle | Ser | Ala | Ser | Phe | Phe | Pro | Ser | Leu |
245 | 250 | 255 | |||||||||||||
Ala | Lys | Lys | Phe | Asn | Arg | Asn | Arg | Leu | Phe | Tyr | Ala | Cys | Xle | Ala | Val |
260 | 265 | 270 | |||||||||||||
Met | Leu | Leu | Gly | lle | Gly | Val | Phe | Ser | Val | Ala | Ser | Gly | Ser | Leu | Ala |
275 | 280 | 285 | |||||||||||||
Leu | Ser | Leu | Val | Gly | Ala | Glu | Phe | Phe | Phe | Xle | Pro | Gin | Pro | Leu | Ala |
290 | 295 | 300 |
Phe 305 | Leu | Val | Val | Leu | Met 310 | lle | lle | Ser | Asp | Ala 315 | Val | Glu | Tyr | Gly | Gin 320 |
Leu | Lys | Thr | Gly | His 325 | Arg | Asp | Glu | Ala | Leu 330 | Thr | Leu | Ser | Val | Arg 335 | Pro |
Leu | Val | Asp | Lys 340 | Leu | Gly | Gly | Ala | Leu 345 | Ser | Asn | Trp | Phe | Val 350 | Ser | Leu |
lle | Ala | Leu 355 | Thr | Ala | Gly | Met | Thr 360 | Thr | Gly | Ala | Thr | Ala 365 | Ser | Thr | lle |
Thr | Ala 370 | His | Gly | Gin | Met | Val 375 | Phe | Lys | Leu | Ala | Met 380 | Phe | Ala | Leu | Pro |
Ala 385 | Val | Met | Leu | Leu | lle 390 | Ala | Val | Ser | lle | Phe 395 | Ala | Lys | Lys | Val | Phe 400 |
Leu | Thr | Glu | Glu | Lys 405 | His | Ala | Glu | lle | Val 410 | Asp | Gin | Leu | Glu | Thr 415 | Gin |
Phe | Ser | Gin | Ser 420 | His | Ala | Gin | Lys | Pro 425 | Ala | Gin | Ala | Glu | Ser 430 | Phe | Thr |
Leu | Ala | Ser 435 | Pro | Val | Ser | Gly | Gin 440 | Leu | Met | Asn | Leu | Asp 445 | Met | Val | Asp |
Asp | Pro 450 | Val | Phe | Ala | Asp | Lys 455 | Lys | Leu | Gly Asp | Gly 460 | Phe | Ala | Leu | Val | |
Pro 465 | Ala | Asp | Gly | Lys | Val 470 | Tyr | Ala | Pro | Phe | Ala 475 | Gly | Thr | Val | Arg | Gin 480 |
Leu | Ala | Lys | Thr | Arg 485 | His | Ser | Xle | Val | Leu 490 | Glu | Asn | Glu | His | Gly 495 | Val |
- 17CZ 302175 B6
Leu | Val | Leu | Ile | His | Leu | Gly | Leu | Gly | Thr | Val | Lys | Leu | Asn | Gly | Thr |
500 | 505 | 510 | |||||||||||||
Gly | Phe | Val | Ser | Tyr | Val | Glu | Glu | Gly | Ser | Gin | Val | Glu | Ala | Gly | Gin |
515 | 520 | 525 | |||||||||||||
Gin | Ile | Leu | Glu | Phe | Trp | Asp | Pro | Ala | Ile | Lys | Gin | Ala | Lys | Leu | Asp |
530 | 535 | 540 | |||||||||||||
Asp | Thr | Val | Ile | Val | Thr | Val | Ile | Asn | Ser | Glu | Thr | Phe | Ala | Asn | Ser |
545 | 550 | 555 | 560 | ||||||||||||
Gin | Met | Leu | Leu | Pro | Ile | Gly | His | Ser | Val | Gin | Ala | Leu | Asp | Asp | Val |
565 | 570 | 575 | |||||||||||||
Phe | Lys | Leu | Glu | Gly | Lys | Asn |
580 <210> 3 <211> 880 <212> PRT <213> Lactobacillus bulgaricus <400> 3
Met 1 | Ser Asn | Lys | Leu 5 | Val Lys | Glu Lys Arg Val Asp Gin Ala Asp Leu | ||||||||||
10 | 15 | ||||||||||||||
Ala | Trp | Leu | Thr | Asp | Pro | Glu | Val | Tyr | Glu | Val | Asn | Thr | Ile | Pro | Pro |
20 | 25 | 30 | |||||||||||||
His | Ser | Asp | His | Glu | Ser | Phe | Gin | Ser | Gin | Glu | Glu | Leu | Glu | Glu | Gly |
35 | 40 | 45 |
Lys | Ser 50 | Ser | Leu | Val | Gin | Ser 55 | Leu | Asp | Gly | Asp | Trp 60 | Leu | Ile | Asp | Tyr |
Ala 65 | Glu | Asn | Gly | Gin | Gly 70 | Pro | Val | Asn | Phe | Tyr 75 | Ala | Glu | Asp | Phe | Asp 80 |
Asp | Ser | Asn | Phe | Lys 85 | Ser | Val | Lys | Val | Pro 90 | Gly | Asn | Leu | Glu | Leu 95 | Gin |
Gly | Phe | Gly | Gin 100 | Pro | Gin | Tyr | Val | Asn 105 | Val | Gin | Tyr | Pro | Trp 110 | Asp | Gly |
Ser | Glu | Glu 115 | Ile | Phe | Pro | Pro | Gin 120 | Ile | Pro | Ser | Lys | Asn 125 | Pro | Leu | Ala |
Ser | Tyr 130 | Val | Arg | Tyr | Phe | Asp 135 | Leu | Asp | Glu | Ala | Phe 140 | Trp | Asp | Lys | Glu |
val 145 | Ser | Leu | Lys | Phe | Asp 150 | Gly | Ala | Ala | Thr | Ala 155 | Ile | Tyr | Val | Trp | Leu 160 |
Asn | Gly | His | Phe | Val 165 | Gly | Tyr | Gly | Glu | Asp 170 | Ser | Phe | Thr | Pro | Ser 175 | Glu |
Phe | Met | Val | Thr 180 | Lys | Phe | Leu | Lys | Lys 185 | Glu | Asn | Asn | Arg | Leu 190 | Ala | Val |
- 18CZ 302175 B6
Ala | Leu | Tyr 195 | Lys | Tyr | Ser | Ser | Ala 200 | Ser | Trp | Leu | Glu | Asp 205 | Gin | Asp | Phe |
Trp | Arg 210 | Met | Ser | Gly | Leu | Phe 215 | Arg | Ser | Val | Thr | Leu 220 | Gin | Ala | Lys | Pro |
Arg 225 | Leu | His | Leu | Glu | Asp 230 | Leu | Lys | Leu | Thr | Ala 235 | Ser | Leu | Thr | Asp | Asn 240 |
Tyr | Gin | Lys | Gly | Lys 245 | Leu | Glu | Val | Glu | Ala 250 | Asn | Ile | Ala | Tyr | Arg 255 | Leu |
Pro | Asn | Ala | Ser 260 | Phe | Lys | Leu | Glu | Val 265 | Arg | Asp | Ser | Glu | Gly 270 | Asp | Leu |
Val | Ala | Glu 275 | Lys | Leu | Gly | Pro | Ile 280 | Arg | Ser | Glu | Gin | Leu 285 | Glu | Phe | Thr |
Leu | Ala 290 | Asp | Leu | Pro | Val | Ala 295 | Ala | Trp | Ser | Ala | Glu 300 | Lys | Pro | Asn | Leu |
Tyr 305 | Gin | Val | Arg | Leu | Tyr 310 | Leu | Tyr | Gin | Ala | Gly 315 | Ser | Leu | Leu | Glu | Val 320 |
Ser | Arg | Gin | Glu | Val 325 | Gly | Phe | Arg | Asn | Phe 330 | Glu | Leu | Lys | Asp | Gly 335 | Ile |
Met | Tyr | Leu | Asn 340 | Gly | Gin | Arg | Ile | val 345 | Phe | Lys | Gly | Ala | Asn 350 | Arg | His |
Glu | Phe | Asp 355 | Ser | Lys | Leu | Gly | Arg 360 | Ala | Ile | Thr | Glu | Glu 365 | Asp | Met | Ile |
Trp | Asp 370 | Ile | Lys | Thr | Met | Lys 375 | Arg | Ser | Asn | Ile | Asn 380 | Ala | Val | Arg | Cys |
Ser 385 | His | Tyr | Pro | Asn | Gin 390 | Ser | Leu | Phe | Tyr | Arg 395 | Leu | Cys | Asp | Lys | Tyr 400 |
Gly | Leu | Tyr | Val | Ile 405 | Asp | Glu | Ala | Asn | Leu 410 | Glu | Ser | His | Gly | Thr 415 | Trp |
Glu | Lys | Val | Gly 420 | Gly | His | Glu | Asp | Pro 425 | Ser | Phe | Asn | Val | Pro 430 | Gly | Asp |
Asp | Gin | His 435 | Trp | Leu | Gly | Ala | Ser 440 | Leu | Ser | Arg | Val | Lys 445 | Asn | Met | Met |
Ala | Arg 450 | Asp | Lys | Asn | His | Ala 455 | Ser | Ile | Leu | Ile | Trp 4 60 | Ser | Leu | Gly | Asn |
Glu 465 | Ser | Tyr | Ala | Gly | Thr 470 | Val | Phe | Ala | Gin | Met 475 | Ala | Asp | Tyr | Val | Arg 480 |
Lys | Ala | Asp | Pro | Thr 485 | Arg | Val | Gin | His | Tyr 490 | Glu | Gly | Val | Thr | His 495 | Asn |
Arg | Lys | Phe | Asp 500 | Asp | Ala | Thr | Gin | Ile 505 | Glu | Ser | Arg | Met | Tyr 510 | Ala | Pro |
Ala | Lys | Val 515 | Ile | Glu | Glu | Tyr | Leu 520 | Thr | Asn | Lys | Pro | Ala 525 | Lys | Pro | Phe |
- 19CZ 302175 B6
Ile | Ser | Val | Glu | Tyr | Ala | His | Ala | Met | Gly | Asn | Ser | Val | Gly | Asp | Leu |
530 | 535 | 540 | |||||||||||||
Ala | Ala | Tyr | Thr | Ala | Leu | Glu | Lys | Tyr | Pro | His | Tyr | Gin | Gly | Gly | Phe |
545 | 550 | 555 | 560 | ||||||||||||
Ile | Trp | Asp | Trp | Ile | Asp | Gin | Gly | Leu | Glu | Lys | Asp | Gly | His | Leu | Leu |
565 | 570 | 575 | |||||||||||||
Tyr | Gly | Gly | Asp | Phe | Asp | Asp | Arg | Pro | Thr | Asp | Tyr | Glu | Phe | Cys | Gly |
580 | 585 | 590 | |||||||||||||
Asn | Gly | Leu | Val | Phe | Ala | Asp | Arg | Thr | Glu | Ser | Pro | Lys | Leu | Ala | Asn |
595 | 600 | 605 | |||||||||||||
Val | Lys | Ala | Leu | Tyr | Ala | Asn | Leu | Lys | Leu | Glu | Val | Lys | Asp | Gly | Gin |
610 | 615 | 620 | |||||||||||||
Leu | Phe | Leu | Lys | Asn | Asp | Asn | Leu | Phe | Thr | Asn | Ser | Ser | Ser | Tyr | Tyr |
625 | 630 | 635 | 640 | ||||||||||||
Phe | Leu | Thr | Ser | Leu | Leu | Val | Asp | Gly | Lys | Leu | Thr | Tyr | Gin | Ser | Arg |
645 | 650 | 655 | |||||||||||||
Pro | Leu | Thr | Phe | Gly | Leu | Glu | Pro | Gly | Glu | Ser | Gly | Thr | Phe' | Ala | Leu |
660 | 665 | 670 | |||||||||||||
Pro | Trp | Pro | Glu | Val | Ala | Asp | Glu | Lys | Gly | Glu | Val | Val | Tyr | Arg | Val |
675 | 680 | 685 | |||||||||||||
Thr | Ala | His | Leu | Lys | Glu | Asp | Leu | Pro | Trp | Ala | Asp | Glu | Gly | Phe | Thr |
690 | 695 | 700 | |||||||||||||
Val | Ala | Glu | Ala | Glu | Glu | Val | Ala | Gin | Lys | Leu | Pro | Glu | Phe | Lys | Pro |
705 | 710 | 715 | 720 | ||||||||||||
Glu | Gly | Arg | Pro | Asp | Leu | Val | Asp | Ser | Asp | Tyr | Asn | Leu | Gly | Leu | Lys |
725 | 730 | 735 | |||||||||||||
Gly | Asn | Asn | Phe | Gin | Ile | Leu | Phe | Ser | Lyš | Val | Lys | Gly | Trp | Pro | Val |
740 | 745 | 750 | |||||||||||||
Ser | Leu | Lys | Tyr | Ala | Gly | Arg | Glu | Tyr | Leu | Lys | Arg | Leu | Pro | Glu | Phe |
755 | 760 | 765 | |||||||||||||
Thr | Phe | Trp | Arg | Ala | Leu | Thr | Asp | Asn | Asp | Arg | Gly | Ala | Gly | Tyr | Gly |
770 | 775 | 780 | |||||||||||||
Tyr | Asp | Leu | Ala | Arg | Trp | Glu | Asn | Ala | Gly | Lys | Tyr | Ala | Arg | Leu | Lys |
785 | 790 | 7 95 | 800 |
Asp lle | Ser | Cys | Glu Val 805 | Lys Glu Asp Ser 810 | Val | Leu Val | Lys | Thr 815 | Ala | ||||||
Phe | Thr | Leu | Pro | Val | Ala | Leu | Lys | Gly | Asp | Leu | Thr | Val | Thr | Tyr | Glu |
820 | 825 | 830 | |||||||||||||
Val | Asp | Gly | Arg | Gly | Lys | Xle | Ala | Val | Thr | Ala | Asp | Phe | Pro | Gly | Ala |
835 | 840 | 845 | |||||||||||||
Glu | Glu | Ala | Gly | Leu | Leu | Pro | Ala | Phe | Gly | Leu | Asn | Leu | Ala | Leu | Pro |
850 | 855 | 860 | |||||||||||||
Lys | Glu | Leu | Thr | Asp | Tyr | Arg | Tyr | Tyr | Gly | Leu | Gly | Pro | Asn | Glu | Ser |
865 | 870 | 875 | 880 |
PATENTOVÉ NÁROKY
Claims (8)
1. Mutantní kmen Lactobacillus bulgaricus, uložený ve sbírce kultur CNCM 14. ledna 1998 pod číslem 1-1968, nesoucí bodovou nonsense mutaci v kódové sekvenci pro β-galaktosidázu a postrádající β-galaktosidázovou aktivitu.
2. Mléčný zákvas, vyznačující se tím, že obsahuje kmen Lactobacillus bulgaricus podle nároku 1.
3. Mléčný zákvas podle nároku 2, vyznačující se tím, že uvedený kmen Lactobacillus bulgaricus je spojen s alespoň jedním kmenem S. thermophilus.
4. Způsob výroby zakvašeného mléčného výrobku, vyznačující se tím, že zahrnuje krok, během nějž se mléko kvasí za použití mléčného zákvasu, zahrnujícího kmen Lactobacillus bulgaricus podle nároku 1 v přítomnosti alespoň jednoho cukru, který může být uvedeným kmenem Lactobacillus bulgaricus asimilován.
5. Způsob podle nároku 4, vyznačující se tím, že cukrem, který může být kmenem Lactobacillus bulgaricus asimilován, je glukóza.
6. Způsob podle kteréhokoliv z nároků 4 nebo 5, vyznačující se tím, že zastavení kvašení se provádí bez ochlazení uvedeného mléčného výrobku,
7. Zakvašený mléčný výrobek, připravitelný způsobem podle kteréhokoliv z nároků 4 až 6.
8. Zakvašený mléčný výrobek podle nároku 7, vyznačující se tím, že tímto výrobkem je jogurt.
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FR9806456A FR2778921B1 (fr) | 1998-05-22 | 1998-05-22 | Souches mutantes de lactobacillus bulgaricus depourvues d'activite beta-galactosidase |
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CZ302175B6 true CZ302175B6 (cs) | 2010-12-01 |
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US (2) | US6875601B1 (cs) |
EP (1) | EP1078074B2 (cs) |
JP (2) | JP4576047B2 (cs) |
AR (1) | AR016496A1 (cs) |
AT (1) | ATE288492T1 (cs) |
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CA (1) | CA2329494C (cs) |
CZ (1) | CZ302175B6 (cs) |
DE (1) | DE69923554T3 (cs) |
DK (1) | DK1078074T3 (cs) |
ES (1) | ES2237099T5 (cs) |
FR (1) | FR2778921B1 (cs) |
HU (1) | HUP0102019A3 (cs) |
IL (3) | IL139812A0 (cs) |
PL (1) | PL202208B1 (cs) |
PT (1) | PT1078074E (cs) |
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FR2778921B1 (fr) * | 1998-05-22 | 2001-05-11 | Gervais Danone Sa | Souches mutantes de lactobacillus bulgaricus depourvues d'activite beta-galactosidase |
MY143693A (en) | 2004-03-24 | 2011-06-30 | Nestec Sa | Shelf stable product wih living micro-organisms |
FR2876874B1 (fr) * | 2004-10-22 | 2007-02-16 | Gervais Danone Sa | Protection d'ingredients alimentaires bioactifs par l'utilisation d'ingredients leurres |
FR2877012B1 (fr) * | 2004-10-22 | 2010-09-10 | Gervais Danone Sa | Souches de streptococcus thermophilus ami deficientes a post-acidification reduite |
FR2876876B1 (fr) * | 2004-10-22 | 2007-02-16 | Gervais Danone Sa | Protection d'ingredients alimentaires bioactifs par l'utilisation de microorganismes presentant une capacite de metabolisation reduite |
FR2886313B1 (fr) * | 2005-05-31 | 2007-08-17 | Gervais Danone Sa | Souches mutantes de bacteries lactiques possedant une lactose permease non phosphorylable. |
FR2895877B1 (fr) * | 2006-01-06 | 2012-06-22 | Gervais Danone Sa | Poudre de lait fermente ou yaourt a haute densite en ferments lactiques |
EP1820851B9 (fr) * | 2006-02-20 | 2012-06-27 | Compagnie Gervais Danone | Souches de Lactobacillus helveticus ne fermentant pas le lactose |
EP2258205A1 (en) * | 2009-06-03 | 2010-12-08 | Yoplait France | Process for manufacturing of a fermented dairy product |
US8555933B2 (en) * | 2009-07-24 | 2013-10-15 | Tyco Electronics Corporation | Wire untwisting tool |
ES2762445T3 (es) | 2011-04-29 | 2020-05-25 | Gervais Danone Sa | Uso de cepas mutantes resistentes a la nisina de lactobacilos para reducir la post-acidificación en productos alimenticios |
SG11201509806UA (en) * | 2013-05-31 | 2015-12-30 | Meiji Co Ltd | Fermented milk that does not undergo increase in acid level, and method for producing same |
CN103275953B (zh) * | 2013-06-25 | 2014-06-18 | 山东大学 | 一种转苷底物特异性拓宽的β-半乳糖苷酶 |
EP3375292A1 (en) * | 2014-06-19 | 2018-09-19 | Chr. Hansen A/S | Method of producing a fermented milk product with improved control of post acidification |
EA034611B1 (ru) | 2014-06-19 | 2020-02-27 | Кхр. Хансен А/С | Способ получения ферментированного молочного продукта с улучшенным контролем последующего подкисления |
MX2018008608A (es) * | 2016-01-21 | 2018-11-19 | Chr Hansen As | Metodo de produccion de un producto lacteo fermentado usando lactobacillus casei. |
WO2018130630A1 (en) | 2017-01-13 | 2018-07-19 | Chr. Hansen A/S | Process for producing a fermented milk product |
MX2019010711A (es) * | 2017-03-28 | 2019-12-11 | Chr Hansen As | Composicion de bacterias de acido lactico para preparar productos alimenticios fermentados con dulzor y sabor natural incrementados. |
US11479763B2 (en) * | 2017-04-07 | 2022-10-25 | Dupont Nutrition Biosciences Aps | Bacillus host cells producing β-galactosidases and lactases in the absence of p-nitrobenzylesterase side activity |
CN114072508B (zh) * | 2019-03-14 | 2024-10-08 | 国际营养与健康丹麦有限公司 | 新的乳酸细菌 |
US20230200406A1 (en) * | 2020-05-29 | 2023-06-29 | Chr. Hansen A/S | Lactic acid bacteria composition for preparing fermented food products |
CN115960757B (zh) * | 2022-10-11 | 2024-04-09 | 南京工业大学 | 一株可以耐受低pH生产L-乳酸的乳酸菌及其应用 |
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1998
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1999
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