Home LiteratureArticle Details
PMID: 14084606 Published · ppublish English Journal Article

THE CONVERSION OF SHIKIMIC ACID INTO CERTAIN AROMATIC COMPOUNDS BY CELL-FREE EXTRACTS OF AEROBACTER AEROGENES AND ESCHERICHIA COLI.

The Biochemical journal ·Vol. 89 ·1963-11-00 ·Pages 229-39

MORGAN PN, GIBSON MI, GIBSON F

Abstract

暂无摘要

Keywords
ADENOSINE TRIPHOSPHATE AEROBACTER AEROGENES ANTHRANILIC ACID CHROMATOGRAPHY ESCHERICHIA COLI EXPERIMENTAL LAB STUDY METABOLISM NAD PHENYLPYRUVIC ACID PYRUVATES SHIKIMIC ACID SPECTROPHOTOMETRY TRYPTOPHAN
MeSH Terms
Adenosine Triphosphate Chromatography Enterobacter aerogenes Escherichia coli Metabolism NAD Phenylpyruvic Acids Pyruvates Research Shikimic Acid Spectrophotometry Tryptophan ortho-Aminobenzoates
Chemicals
Phenylpyruvic Acids Pyruvates ortho-Aminobenzoates NAD anthranilic acid Shikimic Acid Tryptophan Adenosine Triphosphate phenylpyruvic acid
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
MORGAN P N
GIBSON M I
GIBSON F
References (16)
16 references, click to expand
  1. A press for disrupting bacteria and other micro-organisms.
    Br J Exp Pathol. 1951 Apr;32(2):97-109 PMID: 14848424
  2. Protein measurement with the Folin phenol reagent.
    J Biol Chem. 1951 Nov;193(1):265-75 PMID: 14907713
  3. Aromatic biosynthesis. VII. Accumulation of two derivatives of shikimic acid by bacterial mutants.
    J Bacteriol. 1953 Aug;66(2):129-36 PMID: 13084547
  4. Aromatic biosynthesis. XI. The aromatization step in the synthesis of phenylalanine.
    Science. 1954 May 28;119(3100):774-5 PMID: 13168367
  5. Tryptophan metabolism and its relation to phage resistance in Escherichia coli.
    J Gen Microbiol. 1954 Aug;11(1):7-16 PMID: 13192295
  6. A microchemical method for the detection and determination of shikimic acid.
    J Biol Chem. 1958 Feb;230(2):1043-50 PMID: 13525420
  7. The effect of chloramphenicol and oxytetracycline on the formation of intermediates in tryptophan biosynthesis.
    Aust J Exp Biol Med Sci. 1961 Apr;39:171-8 PMID: 13705109
  8. The formation of 4-hydroxyphenylpyruvic acid and phenylpyruvic acid by tryptophan auxotrophs and wild-type Aerobacter aerogenes considered in relation to the general aromatic pathway.
    Biochim Biophys Acta. 1961 Jul 8;50:495-505 PMID: 13724173
  9. Phenolic compounds accumulated by washed cell suspensions of a tryptophan auxotroph of Aerobacter aerogenes.
    Biochim Biophys Acta. 1961 May 27;49:485-94 PMID: 13736115
  10. A possible relationship between the formation of o-dihydric phenols and tryptophan biosynthesis by Aerobacter aerogens.
    Biochim Biophys Acta. 1962 Feb 26;57:290-8 PMID: 14486988
  11. 3-Enolpyruvylshikimate 5-phosphate, an intermediate in the biosynthesis of anthranillate.
    Proc Natl Acad Sci U S A. 1962 May 15;48:864-7 PMID: 14492558
  12. Effects of phencyclidine on the radiosensitivity of mice.
    Nature. 1962 Sep 22;195:1173-5 PMID: 14007035
  13. An isotopic study of the conversion of anthranilic acid to indole.
    J Biol Chem. 1955 Nov;217(1):345-54 PMID: 13271398
  14. False feedback inhibition: inhibition of tryptophan biosynthesis by 5-methyltryptophan.
    J Biol Chem. 1960 Apr;235:1098-102 PMID: 14424820
  15. Aromatic biosynthesis. XVI. Aromatization of prephenic acid to p-hydroxyphenylpyruvic acid, a step in tyrosine biosynthesis in Escherichia coli.
    Biochim Biophys Acta. 1959 Nov;36:102-17 PMID: 14444151
  16. 1-(o-Carboxyphenylamino)-1-deoxyribulose. A compound formed by mutant strains of Aerobacter aerogenes and Escherichia coli blocked in the biosynthesis of tryptophan.
    Biochem J. 1959 Aug;72:586-97 PMID: 13817923
Article Info
Journal
The Biochemical journal
Abbr.
Biochem J
ISSN
0264-6021
Published
1963-11-00
Pages
229-39
Language
English
Region
England
NLM ID
2984726R
PMCID
PMC1202350
Subset
OM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com