TH58895B - Method for processing L-amino acids By using bacteria in the family Enterobacteriaceae In which the expression of the kefB gene was stopped - Google Patents
Method for processing L-amino acids By using bacteria in the family Enterobacteriaceae In which the expression of the kefB gene was stoppedInfo
- Publication number
- TH58895B TH58895B TH601002166A TH0601002166A TH58895B TH 58895 B TH58895 B TH 58895B TH 601002166 A TH601002166 A TH 601002166A TH 0601002166 A TH0601002166 A TH 0601002166A TH 58895 B TH58895 B TH 58895B
- Authority
- TH
- Thailand
- Prior art keywords
- bacteria
- aromatic
- amino acid
- amino acids
- acid
- Prior art date
Links
- 241000894006 Bacteria Species 0.000 title claims abstract 14
- 150000008575 L-amino acids Chemical class 0.000 title claims abstract 14
- 101150065903 kefB gene Proteins 0.000 title claims abstract 6
- 238000000034 method Methods 0.000 title claims abstract 6
- 241000588921 Enterobacteriaceae Species 0.000 title claims abstract 4
- 241000588722 Escherichia Species 0.000 claims abstract 3
- 241000520272 Pantoea Species 0.000 claims abstract 3
- -1 Aromatic L-amino acid Chemical class 0.000 claims 9
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 claims 4
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 claims 4
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 claims 4
- AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 claims 4
- QIVBCDIJIAJPQS-VIFPVBQESA-N L-tryptophane Chemical compound C1=CC=C2C(C[C@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-VIFPVBQESA-N 0.000 claims 4
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims 3
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 claims 2
- PWKSKIMOESPYIA-UHFFFAOYSA-N 2-acetamido-3-sulfanylpropanoic acid Chemical compound CC(=O)NC(CS)C(O)=O PWKSKIMOESPYIA-UHFFFAOYSA-N 0.000 claims 2
- QDGAVODICPCDMU-UHFFFAOYSA-N 2-amino-3-[3-[bis(2-chloroethyl)amino]phenyl]propanoic acid Chemical compound OC(=O)C(N)CC1=CC=CC(N(CCCl)CCCl)=C1 QDGAVODICPCDMU-UHFFFAOYSA-N 0.000 claims 2
- CKLJMWTZIZZHCS-UHFFFAOYSA-N D-OH-Asp Natural products OC(=O)C(N)CC(O)=O CKLJMWTZIZZHCS-UHFFFAOYSA-N 0.000 claims 2
- QNAYBMKLOCPYGJ-UHFFFAOYSA-N D-alpha-Ala Natural products CC([NH3+])C([O-])=O QNAYBMKLOCPYGJ-UHFFFAOYSA-N 0.000 claims 2
- QNAYBMKLOCPYGJ-UWTATZPHSA-N L-Alanine Natural products C[C@@H](N)C(O)=O QNAYBMKLOCPYGJ-UWTATZPHSA-N 0.000 claims 2
- CKLJMWTZIZZHCS-UWTATZPHSA-N L-Aspartic acid Natural products OC(=O)[C@H](N)CC(O)=O CKLJMWTZIZZHCS-UWTATZPHSA-N 0.000 claims 2
- FFEARJCKVFRZRR-UHFFFAOYSA-N L-Methionine Natural products CSCCC(N)C(O)=O FFEARJCKVFRZRR-UHFFFAOYSA-N 0.000 claims 2
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 claims 2
- ODKSFYDXXFIFQN-BYPYZUCNSA-N L-arginine Chemical compound OC(=O)[C@@H](N)CCCN=C(N)N ODKSFYDXXFIFQN-BYPYZUCNSA-N 0.000 claims 2
- 229930064664 L-arginine Natural products 0.000 claims 2
- 235000014852 L-arginine Nutrition 0.000 claims 2
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 claims 2
- ZDXPYRJPNDTMRX-VKHMYHEASA-N L-glutamine Chemical compound OC(=O)[C@@H](N)CCC(N)=O ZDXPYRJPNDTMRX-VKHMYHEASA-N 0.000 claims 2
- 229930182816 L-glutamine Natural products 0.000 claims 2
- AGPKZVBTJJNPAG-WHFBIAKZSA-N L-isoleucine Chemical compound CC[C@H](C)[C@H](N)C(O)=O AGPKZVBTJJNPAG-WHFBIAKZSA-N 0.000 claims 2
- 229930182844 L-isoleucine Natural products 0.000 claims 2
- 239000004395 L-leucine Substances 0.000 claims 2
- 235000019454 L-leucine Nutrition 0.000 claims 2
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 claims 2
- 229930195722 L-methionine Natural products 0.000 claims 2
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 claims 2
- 239000004473 Threonine Substances 0.000 claims 2
- 229960003767 alanine Drugs 0.000 claims 2
- 229960005261 aspartic acid Drugs 0.000 claims 2
- 229960002989 glutamic acid Drugs 0.000 claims 2
- 229960002885 histidine Drugs 0.000 claims 2
- 229960000310 isoleucine Drugs 0.000 claims 2
- 229960003136 leucine Drugs 0.000 claims 2
- 229960004452 methionine Drugs 0.000 claims 2
- WPLOVIFNBMNBPD-ATHMIXSHSA-N subtilin Chemical compound CC1SCC(NC2=O)C(=O)NC(CC(N)=O)C(=O)NC(C(=O)NC(CCCCN)C(=O)NC(C(C)CC)C(=O)NC(=C)C(=O)NC(CCCCN)C(O)=O)CSC(C)C2NC(=O)C(CC(C)C)NC(=O)C1NC(=O)C(CCC(N)=O)NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C1NC(=O)C(=C/C)/NC(=O)C(CCC(N)=O)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)CNC(=O)C(NC(=O)C(NC(=O)C2NC(=O)CNC(=O)C3CCCN3C(=O)C(NC(=O)C3NC(=O)C(CC(C)C)NC(=O)C(=C)NC(=O)C(CCC(O)=O)NC(=O)C(NC(=O)C(CCCCN)NC(=O)C(N)CC=4C5=CC=CC=C5NC=4)CSC3)C(C)SC2)C(C)C)C(C)SC1)CC1=CC=CC=C1 WPLOVIFNBMNBPD-ATHMIXSHSA-N 0.000 claims 2
- 229960002898 threonine Drugs 0.000 claims 2
- 229960004799 tryptophan Drugs 0.000 claims 2
- 239000004471 Glycine Substances 0.000 claims 1
- XUIIKFGFIJCVMT-LBPRGKRZSA-N L-thyroxine Chemical compound IC1=CC(C[C@H]([NH3+])C([O-])=O)=CC(I)=C1OC1=CC(I)=C(O)C(I)=C1 XUIIKFGFIJCVMT-LBPRGKRZSA-N 0.000 claims 1
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical compound CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 claims 1
- 241001024304 Mino Species 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 230000002378 acidificating effect Effects 0.000 claims 1
- 230000001580 bacterial effect Effects 0.000 claims 1
- 229950008325 levothyroxine Drugs 0.000 claims 1
- 239000013587 production medium Substances 0.000 claims 1
- 229960001153 serine Drugs 0.000 claims 1
- 229960004441 tyrosine Drugs 0.000 claims 1
Abstract
DC60 การประดิษฐ์ปัจจุบันได้จัดให้มีวิธีสำหรับการผลิต กรดแอล-อะมิโน โดยการใช้แบคทีเรีย ในตระกูล Enterobacteriaceae โดยเฉพาะแบคทีเรียที่อยู่ในสกุล Escherichia หรือ Pantoea ซึ่ง ถูกดัดแปลงเพื่อให้มีการหยุดการแสดงออกของยีน kefB การประดิษฐ์ปัจจุบันได้จัดให้มีวิธีสำหรับการผลิต กรดแอล-อะมิโน โดยการใช้แบคทีเรีย ในตระกูล Enterobacteriaceae โดยเฉพาะแบคทีเรียที่อยู่ในสกุล Escherichia หรือ Pantoea ซึ่ง ถูกดัดแปลงเพื่อให้มีการหยุดการแสดงออกของยีน kefB DC60, the current invention provides a method for its production. L-Amino Acid By using bacteria in the family Enterobacteriaceae. Especially bacteria belonging to the genus Escherichia or Pantoea, which have been modified to stop the expression of the kefB gene. L-Amino Acid By using bacteria in the family Enterobacteriaceae. Especially bacteria belonging to the genus Escherichia or Pantoea, which have been modified to stop the expression of the kefB gene.
Claims (1)
Publications (3)
| Publication Number | Publication Date |
|---|---|
| TH85273A TH85273A (en) | 2007-06-28 |
| TH85273B TH85273B (en) | 2007-06-28 |
| TH58895B true TH58895B (en) | 2017-11-10 |
Family
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