TH2454A - Process for producing L-Phenylalanine - Google Patents
Process for producing L-PhenylalanineInfo
- Publication number
- TH2454A TH2454A TH8501000009A TH8501000009A TH2454A TH 2454 A TH2454 A TH 2454A TH 8501000009 A TH8501000009 A TH 8501000009A TH 8501000009 A TH8501000009 A TH 8501000009A TH 2454 A TH2454 A TH 2454A
- Authority
- TH
- Thailand
- Prior art keywords
- phenylalanine
- source
- preparation
- partic
- producing
- Prior art date
Links
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 title claims abstract 10
- 229960005190 phenylalanine Drugs 0.000 title claims abstract 6
- 238000000034 method Methods 0.000 title claims abstract 5
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 claims abstract 2
- 238000002360 preparation method Methods 0.000 claims abstract 2
- 241000588724 Escherichia coli Species 0.000 claims 1
- 241000589516 Pseudomonas Species 0.000 claims 1
- 102000003929 Transaminases Human genes 0.000 claims 1
- 108090000340 Transaminases Proteins 0.000 claims 1
- 239000003929 acidic solution Substances 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 230000000813 microbial effect Effects 0.000 claims 1
- 244000005700 microbiome Species 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 230000020477 pH reduction Effects 0.000 claims 1
- 150000002994 phenylalanines Chemical class 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 239000007858 starting material Substances 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 239000006227 byproduct Substances 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 238000000354 decomposition reaction Methods 0.000 abstract 1
- KHPXUQMNIQBQEV-UHFFFAOYSA-N oxaloacetic acid Chemical group OC(=O)CC(=O)C(O)=O KHPXUQMNIQBQEV-UHFFFAOYSA-N 0.000 abstract 1
- 239000002243 precursor Substances 0.000 abstract 1
- 238000005891 transamination reaction Methods 0.000 abstract 1
Abstract
กรรมวิธีที่เปิดเผยนี้แสดงถึงการเตรียม แอล-เฟนิลอะลานีนจากสารตั้งต้นของเฟนิลอะลานีน โดยปฏิกริยาทรานซามิเนชันทางชีว ภาพซึ่งทำให้เกิดอย่างสมบูรณ์ กรดแอลพาร์ติคเป็นที่นิยมใช้เป็น แหล่งให้หมู่อะมิโนเพียงแหล่งเดียว และการสลายตัวของกรดออกซา โลอะซีติก ซึ่งเป็นผลิตภัณฑ์พลอยได้เป็นผลให้ปฏิกริยาเกิดขึ้น อย่างสมบูรณ์ The process disclosed here illustrate the preparation of L-phenylalanine from phenylalanine precursors By biological transamination reactions The image which caused it completely L-Partic Acid is commonly used as One source for amino groups And the decomposition of oxaloacetic acid, a by-product, results in a complete reaction.
Claims (3)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TH2454A true TH2454A (en) | 1985-05-01 |
Family
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