JPS6120274B2 - - Google Patents

Info

Publication number: JPS6120274B2
Authority: JP; Japan
Prior art keywords: formula; keto; acid; cooh; culture
Prior art date: 1978-09-22
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.): Expired

Application number

JP11599078A

Other languages

English (en)

Japanese (ja)

Other versions

JPS5542550A (en

Inventor

Kenkichi Takagi

Minoru Masuda

Akinori Naito

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Nippon Kayaku Co Ltd

Original Assignee

Nippon Kayaku Co Ltd

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.)

1978-09-22

Filing date

1978-09-22

Publication date

1986-05-21

1978-09-22 Application filed by Nippon Kayaku Co Ltd filed Critical Nippon Kayaku Co Ltd

1978-09-22 Priority to JP11599078A priority Critical patent/JPS5542550A/ja

1980-03-25 Publication of JPS5542550A publication Critical patent/JPS5542550A/ja

1986-05-21 Publication of JPS6120274B2 publication Critical patent/JPS6120274B2/ja

Status Granted legal-status Critical Current

Links

150000004716 alpha keto acids Chemical class 0.000 claims description 19
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244000005700 microbiome Species 0.000 claims description 13
102000016938 Catalase Human genes 0.000 claims description 9
108010053835 Catalase Proteins 0.000 claims description 9
238000004519 manufacturing process Methods 0.000 claims description 7
150000003839 salts Chemical class 0.000 claims description 6
241001480014 Trigonopsis Species 0.000 claims description 5
235000008206 alpha-amino acids Nutrition 0.000 claims description 5
150000001370 alpha-amino acid derivatives Chemical class 0.000 claims description 4
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
125000000896 monocarboxylic acid group Chemical group 0.000 claims description 3
230000000813 microbial effect Effects 0.000 claims description 2
150000001371 alpha-amino acids Chemical class 0.000 claims 1
238000006243 chemical reaction Methods 0.000 description 12
239000000243 solution Substances 0.000 description 11
238000000034 method Methods 0.000 description 10
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235000013399 edible fruits Nutrition 0.000 description 1
230000000694 effects Effects 0.000 description 1
235000020776 essential amino acid Nutrition 0.000 description 1
239000003797 essential amino acid Substances 0.000 description 1
-1 etc. Chemical compound 0.000 description 1
238000001914 filtration Methods 0.000 description 1
230000008014 freezing Effects 0.000 description 1
238000007710 freezing Methods 0.000 description 1
229930182830 galactose Natural products 0.000 description 1
235000011187 glycerol Nutrition 0.000 description 1
239000001963 growth medium Substances 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
150000003840 hydrochlorides Chemical class 0.000 description 1
FGKJLKRYENPLQH-UHFFFAOYSA-N isocaproic acid Chemical compound CC(C)CCC(O)=O FGKJLKRYENPLQH-UHFFFAOYSA-N 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
229910052748 manganese Inorganic materials 0.000 description 1
239000011572 manganese Substances 0.000 description 1
235000012054 meals Nutrition 0.000 description 1
235000013379 molasses Nutrition 0.000 description 1
229910000403 monosodium phosphate Inorganic materials 0.000 description 1
235000019799 monosodium phosphate Nutrition 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
229910017464 nitrogen compound Inorganic materials 0.000 description 1
150000002830 nitrogen compounds Chemical class 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
230000003204 osmotic effect Effects 0.000 description 1
238000005895 oxidative decarboxylation reaction Methods 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
230000001376 precipitating effect Effects 0.000 description 1
239000003531 protein hydrolysate Substances 0.000 description 1
230000008085 renal dysfunction Effects 0.000 description 1
UQDJGEHQDNVPGU-UHFFFAOYSA-N serine phosphoethanolamine Chemical compound [NH3+]CCOP([O-])(=O)OCC([NH3+])C([O-])=O UQDJGEHQDNVPGU-UHFFFAOYSA-N 0.000 description 1
FHHPUSMSKHSNKW-SMOYURAASA-M sodium deoxycholate Chemical compound [Na+].C([C@H]1CC2)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC([O-])=O)C)[C@@]2(C)[C@@H](O)C1 FHHPUSMSKHSNKW-SMOYURAASA-M 0.000 description 1
AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
235000011121 sodium hydroxide Nutrition 0.000 description 1
239000004317 sodium nitrate Substances 0.000 description 1
235000010344 sodium nitrate Nutrition 0.000 description 1
XZTJQQLJJCXOLP-UHFFFAOYSA-M sodium;decyl sulfate Chemical compound [Na+].CCCCCCCCCCOS([O-])(=O)=O XZTJQQLJJCXOLP-UHFFFAOYSA-M 0.000 description 1
229940035044 sorbitan monolaurate Drugs 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000008107 starch Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
WWJZWCUNLNYYAU-UHFFFAOYSA-N temephos Chemical compound C1=CC(OP(=S)(OC)OC)=CC=C1SC1=CC=C(OP(=S)(OC)OC)C=C1 WWJZWCUNLNYYAU-UHFFFAOYSA-N 0.000 description 1
238000010257 thawing Methods 0.000 description 1
238000009210 therapy by ultrasound Methods 0.000 description 1
GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
208000009852 uremia Diseases 0.000 description 1
239000012138 yeast extract Substances 0.000 description 1

Landscapes

Preparation Of Compounds By Using Micro-Organisms (AREA)

JP11599078A 1978-09-22 1978-09-22 Production of alpha-ketoacid Granted JPS5542550A (en)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP11599078A JPS5542550A (en)	1978-09-22	1978-09-22	Production of alpha-ketoacid

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP11599078A JPS5542550A (en)	1978-09-22	1978-09-22	Production of alpha-ketoacid

Publications (2)

Publication Number	Publication Date
JPS5542550A JPS5542550A (en)	1980-03-25
JPS6120274B2 true JPS6120274B2 (fr)	1986-05-21

Family

ID=14676125

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP11599078A Granted JPS5542550A (en)	1978-09-22	1978-09-22	Production of alpha-ketoacid

Country Status (1)

Country	Link
JP (1)	JPS5542550A (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
SE7900826L (sv) *	1979-03-27	1980-09-28	Brodelius P	Anvendning av immobiliserade mikrobiella enzym/cellsystem for framstellning av alfa-ketosyror ur motsvarande aminosyror
FR2517914B1 (fr) *	1981-12-07	1986-02-07	Labo Cent Telecommunicat	Equipement de retransmission de signal de television en voie commune, a commande automatique du rapport image/son
WO2010139527A2 (fr) *	2009-06-05	2010-12-09	Evonik Degussa Gmbh	Procédé de préparation d'acide 2-céto-carboxylique

1978
- 1978-09-22 JP JP11599078A patent/JPS5542550A/ja active Granted

Also Published As

Publication number	Publication date
JPS5542550A (en)	1980-03-25

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JP2004254690A (ja)	2004-09-16	Ｄｌ−メチオニンの製造法
JPS63157990A (ja)	1988-06-30	Ｌ−α−メチルフエニルアラニン類の製造法
JP2674076B2 (ja)	1997-11-05	Ｄ−α−アミノ酸の製造方法
JPS6258710B2 (fr)	1987-12-07
JP2002034584A (ja)	2002-02-05	α−ヒドロキシ酸アンモニウム塩の製造法
GB1577087A (en)	1980-10-15	Enzyme preparation having l-amino acyl amidase activity
JPWO2003062437A1 (ja)	2005-05-26	α−ヒドロキシ酸アンモニウム塩の製造法
WO1996031616A1 (fr)	1996-10-10	Procede de production d'acide l-2-aminoadipique
EP0315786A1 (fr)	1989-05-17	Procédé de préparation d'un acide aminé d-alpha à partir du céto-acide alpha correspondant
JP2507465B2 (ja)	1996-06-12	Ｄ−アスパラギン酸の製造法
JPH01277499A (ja)	1989-11-07	Ｌ−α−アミノ酸の製造法
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JPS5918994B2 (ja)	1984-05-01	Ｄ−Ｎ−カルバミル（ｐ−ヒドロキシフエニル）グリシンの製造法
JPS58175491A (ja)	1983-10-14	Ｌ−フエニルアラニンの製造法
JPS6316119B2 (fr)	1988-04-07
JPS6219093A (ja)	1987-01-27	Ｌ−フエニルアラニンの製造方法