SU502019A1 - Штамм - Google Patents

Штамм

Info

Publication number: SU502019A1
Authority: SU; USSR - Soviet Union
Prior art keywords: medium; acid; brevibacterium; strain; round
Prior art date: 1973-10-11

Application number

SU1959952A

Other languages

English (en)

Russian (ru)

Inventor

Василий Николаевич Букин

Мартин Екабович Бекер

Лидия Сергеевна Куцева

Наталия Михайловна Баздырева

Атис Алфредович Лацар

Ирена Яновна Калване

Атис Карлович Седвалдс

Майя Павловна Руклиша

Валентина Францевна Бекер

Улдис Эрнестович Виестур

Гунар Карлович Лиепиньш

Андрей Робертович Вальдман

Зайга Арлидовна Виестуре

Александр Михайлович Лужков

Лидия Яковлевна Арешкина

Original Assignee

Институт Биохимии Им. А.Н.Баха Ан Ссср

Институт Микробиологии Им. А.Кирхенштейна Ан Латвийской Сср

Priority date (The priority date 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 date listed.)

1973-10-11

Filing date

1973-10-11

Publication date

1976-02-05

1973-10-11 Application filed by Институт Биохимии Им. А.Н.Баха Ан Ссср, Институт Микробиологии Им. А.Кирхенштейна Ан Латвийской Сср filed Critical Институт Биохимии Им. А.Н.Баха Ан Ссср

1973-10-11 Priority to SU1959952A priority Critical patent/SU502019A1/ru

1974-09-09 Priority to AT725774A priority patent/AT340858B/de

1974-09-13 Priority to NL7412148A priority patent/NL7412148A/xx

1974-09-16 Priority to FR7431272A priority patent/FR2247538B1/fr

1974-09-16 Priority to CS634774A priority patent/CS167192B1/cs

1974-09-16 Priority to DD18112074A priority patent/DD115506A1/xx

1974-09-25 Priority to GB4162974A priority patent/GB1456923A/en

1974-09-27 Priority to IE201474A priority patent/IE39920B1/xx

1974-10-01 Priority to BR814574A priority patent/BR7408145D0/pt

1974-10-01 Priority to IT4168674A priority patent/IT1033580B/it

1974-10-03 Priority to DE19742447274 priority patent/DE2447274A1/de

1974-10-10 Priority to BE149383A priority patent/BE820901A/fr

1976-02-05 Application granted granted Critical

1976-02-05 Publication of SU502019A1 publication Critical patent/SU502019A1/ru

Links

239000002609 medium Substances 0.000 description 8
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
241000186146 Brevibacterium Species 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 description 4
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
229910052799 carbon Inorganic materials 0.000 description 4
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
238000000855 fermentation Methods 0.000 description 3
230000004151 fermentation Effects 0.000 description 3
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical group O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
102000016938 Catalase Human genes 0.000 description 2
108010053835 Catalase Proteins 0.000 description 2
AUNGANRZJHBGPY-UHFFFAOYSA-N D-Lyxoflavin Natural products OCC(O)C(O)C(O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-UHFFFAOYSA-N 0.000 description 2
229930091371 Fructose Natural products 0.000 description 2
239000005715 Fructose Substances 0.000 description 2
RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 2
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 2
239000001888 Peptone Substances 0.000 description 2
108010080698 Peptones Proteins 0.000 description 2
229930006000 Sucrose Natural products 0.000 description 2
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 2
239000004202 carbamide Substances 0.000 description 2
239000001913 cellulose Substances 0.000 description 2
229920002678 cellulose Polymers 0.000 description 2
GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
235000019441 ethanol Nutrition 0.000 description 2
OVBPIULPVIDEAO-LBPRGKRZSA-N folic acid Chemical compound C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-LBPRGKRZSA-N 0.000 description 2
239000008103 glucose Substances 0.000 description 2
HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 description 2
230000007062 hydrolysis Effects 0.000 description 2
238000006460 hydrolysis reaction Methods 0.000 description 2
239000002054 inoculum Substances 0.000 description 2
-1 mgltozy Chemical compound 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
235000019319 peptone Nutrition 0.000 description 2
229960002477 riboflavin Drugs 0.000 description 2
235000019192 riboflavin Nutrition 0.000 description 2
239000002151 riboflavin Substances 0.000 description 2
239000005720 sucrose Substances 0.000 description 2
OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
239000004254 Ammonium phosphate Substances 0.000 description 1
239000004475 Arginine Substances 0.000 description 1
241000283690 Bos taurus Species 0.000 description 1
239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 1
108010010803 Gelatin Proteins 0.000 description 1
235000019766 L-Lysine Nutrition 0.000 description 1
ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 description 1
CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 1
HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 description 1
FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 description 1
AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 description 1
OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 1
239000004472 Lysine Substances 0.000 description 1
GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 1
WYZDXEKUWRCKOB-YDSAWKJFSA-N Mestanolone Chemical compound C([C@@H]1CC2)C(=O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@](C)(O)[C@@]2(C)CC1 WYZDXEKUWRCKOB-YDSAWKJFSA-N 0.000 description 1
OVBPIULPVIDEAO-UHFFFAOYSA-N N-Pteroyl-L-glutaminsaeure Natural products C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)NC(CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-UHFFFAOYSA-N 0.000 description 1
229920000388 Polyphosphate Polymers 0.000 description 1
208000030555 Pygmy Diseases 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
AYFVYJQAPQTCCC-UHFFFAOYSA-N Threonine Natural products CC(O)C(N)C(O)=O AYFVYJQAPQTCCC-UHFFFAOYSA-N 0.000 description 1
239000004473 Threonine Substances 0.000 description 1
108010046334 Urease Proteins 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
229940037003 alum Drugs 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
235000019270 ammonium chloride Nutrition 0.000 description 1
229910000148 ammonium phosphate Inorganic materials 0.000 description 1
ZRIUUUJAJJNDSS-UHFFFAOYSA-N ammonium phosphates Chemical class [NH4+].[NH4+].[NH4+].[O-]P([O-])([O-])=O ZRIUUUJAJJNDSS-UHFFFAOYSA-N 0.000 description 1
235000019289 ammonium phosphates Nutrition 0.000 description 1
BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
229910052921 ammonium sulfate Inorganic materials 0.000 description 1
239000001166 ammonium sulphate Substances 0.000 description 1
235000011130 ammonium sulphate Nutrition 0.000 description 1
230000002547 anomalous effect Effects 0.000 description 1
ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 1
235000003704 aspartic acid Nutrition 0.000 description 1
OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 1
235000013877 carbamide Nutrition 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
238000001035 drying Methods 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
229960000304 folic acid Drugs 0.000 description 1
235000019152 folic acid Nutrition 0.000 description 1
239000011724 folic acid Substances 0.000 description 1
229930182830 galactose Natural products 0.000 description 1
229920000159 gelatin Polymers 0.000 description 1
239000008273 gelatin Substances 0.000 description 1
235000019322 gelatine Nutrition 0.000 description 1
235000011852 gelatine desserts Nutrition 0.000 description 1
125000001475 halogen functional group Chemical group 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
229930182817 methionine Natural products 0.000 description 1
238000000034 method Methods 0.000 description 1
230000002906 microbiologic effect Effects 0.000 description 1
239000000203 mixture Substances 0.000 description 1
235000013379 molasses Nutrition 0.000 description 1
238000005192 partition Methods 0.000 description 1
239000001205 polyphosphate Substances 0.000 description 1
235000011176 polyphosphates Nutrition 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000013587 production medium Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
WBHQBSYUUJJSRZ-UHFFFAOYSA-M sodium bisulfate Chemical compound [Na+].OS([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-M 0.000 description 1
229910000342 sodium bisulfate Inorganic materials 0.000 description 1
238000009331 sowing Methods 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000008174 sterile solution Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
229910021653 sulphate ion Inorganic materials 0.000 description 1
OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/04—Alpha- or beta- amino acids
- C12P13/08—Lysine; Diaminopimelic acid; Threonine; Valine

Landscapes

Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Zoology (AREA)
Life Sciences & Earth Sciences (AREA)
Wood Science & Technology (AREA)
Chemical Kinetics & Catalysis (AREA)
Microbiology (AREA)
General Chemical & Material Sciences (AREA)
Biotechnology (AREA)
Health & Medical Sciences (AREA)
Biochemistry (AREA)
Bioinformatics & Cheminformatics (AREA)
General Engineering & Computer Science (AREA)
General Health & Medical Sciences (AREA)
Genetics & Genomics (AREA)
Preparation Of Compounds By Using Micro-Organisms (AREA)
Enzymes And Modification Thereof (AREA)
Micro-Organisms Or Cultivation Processes Thereof (AREA)

SU1959952A 1973-10-11 1973-10-11 Штамм SU502019A1 (ru)

Priority Applications (12)

Application Number	Priority Date	Filing Date	Title
SU1959952A SU502019A1 (ru)	1973-10-11	1973-10-11	Штамм
AT725774A AT340858B (de)	1973-10-11	1974-09-09	Verfahren zur herstellung von l-lysin
NL7412148A NL7412148A (nl)	1973-10-11	1974-09-13	Werkwijze voor het bereiden van l-lysine.
CS634774A CS167192B1 (fr)	1973-10-11	1974-09-16
FR7431272A FR2247538B1 (fr)	1973-10-11	1974-09-16
DD18112074A DD115506A1 (fr)	1973-10-11	1974-09-16
GB4162974A GB1456923A (en)	1973-10-11	1974-09-25	Process for the production of l-lysine
IE201474A IE39920B1 (en)	1973-10-11	1974-09-27	Process for the production of 1-lysine
BR814574A BR7408145D0 (pt)	1973-10-11	1974-10-01	Processo para a producao de l-lisina
IT4168674A IT1033580B (it)	1973-10-11	1974-10-01	Procedimento di ottenimento di l lisina
DE19742447274 DE2447274A1 (de)	1973-10-11	1974-10-03	Verfahren zur herstellung von l-lysin
BE149383A BE820901A (fr)	1973-10-11	1974-10-10	Procede de preparation de l-lysine

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
SU1959952A SU502019A1 (ru)	1973-10-11	1973-10-11	Штамм

Publications (1)

Publication Number	Publication Date
SU502019A1 true SU502019A1 (ru)	1976-02-05

Family

ID=20564688

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SU1959952A SU502019A1 (ru)	1973-10-11	1973-10-11	Штамм

Country Status (12)

Country	Link
AT (1)	AT340858B (fr)
BE (1)	BE820901A (fr)
BR (1)	BR7408145D0 (fr)
CS (1)	CS167192B1 (fr)
DD (1)	DD115506A1 (fr)
DE (1)	DE2447274A1 (fr)
FR (1)	FR2247538B1 (fr)
GB (1)	GB1456923A (fr)
IE (1)	IE39920B1 (fr)
IT (1)	IT1033580B (fr)
NL (1)	NL7412148A (fr)
SU (1)	SU502019A1 (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE19932059A1 (de) *	1999-07-12	2001-01-18	Basf Ag	Verfahren zur Herstellung und Verwendung von Lysinbase-Trockenpulvern
CN112779180A (zh) *	2020-12-23	2021-05-11	中国科学院微生物研究所	一种液体发酵培养基及其应用

1973
- 1973-10-11 SU SU1959952A patent/SU502019A1/ru active
1974
- 1974-09-09 AT AT725774A patent/AT340858B/de not_active IP Right Cessation
- 1974-09-13 NL NL7412148A patent/NL7412148A/xx unknown
- 1974-09-16 FR FR7431272A patent/FR2247538B1/fr not_active Expired
- 1974-09-16 DD DD18112074A patent/DD115506A1/xx unknown
- 1974-09-16 CS CS634774A patent/CS167192B1/cs unknown
- 1974-09-25 GB GB4162974A patent/GB1456923A/en not_active Expired
- 1974-09-27 IE IE201474A patent/IE39920B1/xx unknown
- 1974-10-01 BR BR814574A patent/BR7408145D0/pt unknown
- 1974-10-01 IT IT4168674A patent/IT1033580B/it active
- 1974-10-03 DE DE19742447274 patent/DE2447274A1/de active Pending
- 1974-10-10 BE BE149383A patent/BE820901A/fr not_active IP Right Cessation

Also Published As

Publication number	Publication date
GB1456923A (en)	1976-12-01
AT340858B (de)	1978-01-10
NL7412148A (nl)	1975-04-15
DD115506A1 (fr)	1975-10-05
FR2247538A1 (fr)	1975-05-09
DE2447274A1 (de)	1975-04-30
IE39920B1 (en)	1979-01-31
BE820901A (fr)	1975-04-10
IT1033580B (it)	1979-08-10
ATA725774A (de)	1977-05-15
BR7408145D0 (pt)	1975-09-16
FR2247538B1 (fr)	1976-10-22
IE39920L (en)	1975-04-11
CS167192B1 (fr)	1976-04-29

Publication	Publication Date	Title
KR20090004940A (ko)	2009-01-12	폴리비닐 알코올 겔 내에 고정화된 효소 또는 미생물 형태의 생체촉매의 산업적 생산 방법, 이의 사용 방법, 및 이의 생산 장치
SU502019A1 (ru)	1976-02-05	Штамм
Burkholder	1943	Synthesis of riboflavin by a yeast
SU494040A1 (ru)	1978-04-15	Способ получени -лизина
Shaw et al.	1964	BIOSYNTHESIS OF NITRO COMPOUNDS I: Nitrogen and Carbon Requirements for the Biosynthesis of β-Nitropropionic Acid by Penicillium atrovenetum
Mäkinen	1972	Enzyme dynamics of a cariogenic streptococcus: the effect of xylitol and sorbitol
SU526660A1 (ru)	1976-08-30	Штамм N 806-продуцент 2 кето- гулоной кислоты
Passmore et al.	1937	The effect of carbohydrates and allied substances on urease production by Proteus vulgaris
CN100360667C (zh)	2008-01-09	透性化细胞海藻糖合酶及其制备和用途
SU984405A3 (ru)	1982-12-23	Способ получени @ - @ -аминокислот
US2775540A (en)	1956-12-25	Production of dextran
SU745942A1 (ru)	1980-07-07	Способ выращивани
SU379624A1 (fr)	1973-04-20
JPS637753B2 (fr)	1988-02-18
SU622282A1 (ru)	1981-12-23	Способ получени ферментного препарата N-ацетил-глюкозаминидазы
GB1147229A (en)	1969-04-02	Process for producing l-lysine from 5-(4-aminobutyl)-hydantoin
JPS6291177A (ja)	1987-04-25	セレン含有微生物菌体
GB598177A (en)	1948-02-12	Improvements in or relating to process for the production of pantothenic acid
SU386006A1 (ru)	1973-06-14	БИБЛИОТЕКАН. М. Баздырева, Г. К. Лйепиньш, Я. Я. Лаукевиц, У. Э. Виестур,С. Э. Селга, А. Р. Валдман, В. Ф. Бекер, А. К. Седвалдс, А. А. Лацарс,Э. В. Цедере, Р. П. Зелтын и Э. Б. Трусле
Kligler	1916	Some regulating factors in bacterial metabolism
US2494514A (en)	1950-01-10	Production of the amylase of bacillus macerans
SU487116A1 (ru)	1975-10-05	Штамм дрожжей к-1
Erickson et al.	1922	Cultivation of the gonococcus
US4861715A (en)	1989-08-29	Process for the production of nourseothricine and its adsorbate
Nhan et al.	1976	Studies on the rate of lysine production by Brevibacterium lactofermentum from glucose