Literature DB >> 8405922

Isoprenoid biosynthesis in bacteria: two different pathways?

S Horbach1, H Sahm, R Welle.   

Abstract

The biosynthesis of isopentenylpyrophosphate, a central intermediate of isoprenoid formation, was investigated in six different bacterial organisms. Cell-free extracts of Myxococcus fulvus, Staphylococcus carnosus, Lactobacillus plantarum and Halobacterium cutirubrum converted [14C]acetyl-CoA or [14C]hydroxymethylglutaryl-CoA to [14C]mevalonic acid. Furthermore, [14C]mevalonic acid, [14C]mevalonate-5-phosphate and [14C]mevalonate-5-pyrophosphate were metabolized to [14C]isopentenylpyrophosphate. These data demonstrated the in vitro operation of acetoacetate pathway for the formation of isopentenylpyrophosphate in bacteria. In contrast, no intermediates of this reaction sequence could be detected using cell-free extracts of Zymomonas mobilis and Escherichia coli. These results indicate that at least two different pathways for the biosynthesis of isopentenylpyrophosphate are present in bacteria.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8405922     DOI: 10.1111/j.1574-6968.1993.tb06375.x

Source DB:  PubMed          Journal:  FEMS Microbiol Lett        ISSN: 0378-1097            Impact factor:   2.742


  16 in total

Review 1.  Targeting the formation of the cell wall core of M. tuberculosis.

Authors:  Clifton E Barry; Dean C Crick; Michael R McNeil
Journal:  Infect Disord Drug Targets       Date:  2007-06

Review 2.  Mechanistic aspects of carotenoid biosynthesis.

Authors:  Alexander R Moise; Salim Al-Babili; Eleanore T Wurtzel
Journal:  Chem Rev       Date:  2013-10-31       Impact factor: 60.622

3.  Cloning and characterization of a gene from Escherichia coli encoding a transketolase-like enzyme that catalyzes the synthesis of D-1-deoxyxylulose 5-phosphate, a common precursor for isoprenoid, thiamin, and pyridoxol biosynthesis.

Authors:  L M Lois; N Campos; S R Putra; K Danielsen; M Rohmer; A Boronat
Journal:  Proc Natl Acad Sci U S A       Date:  1998-03-03       Impact factor: 11.205

4.  Isoprenoid biosynthesis in bacteria: a novel pathway for the early steps leading to isopentenyl diphosphate.

Authors:  M Rohmer; M Knani; P Simonin; B Sutter; H Sahm
Journal:  Biochem J       Date:  1993-10-15       Impact factor: 3.857

5.  Identification, evolution, and essentiality of the mevalonate pathway for isopentenyl diphosphate biosynthesis in gram-positive cocci.

Authors:  E I Wilding; J R Brown; A P Bryant; A F Chalker; D J Holmes; K A Ingraham; S Iordanescu; C Y So; M Rosenberg; M N Gwynn
Journal:  J Bacteriol       Date:  2000-08       Impact factor: 3.490

6.  A gene cluster for the mevalonate pathway from Streptomyces sp. Strain CL190.

Authors:  M Takagi; T Kuzuyama; S Takahashi; H Seto
Journal:  J Bacteriol       Date:  2000-08       Impact factor: 3.490

7.  Synthesis of CDP-activated ribitol for teichoic acid precursors in Streptococcus pneumoniae.

Authors:  Stefanie Baur; Jon Marles-Wright; Stephan Buckenmaier; Richard J Lewis; Waldemar Vollmer
Journal:  J Bacteriol       Date:  2008-12-12       Impact factor: 3.490

8.  Purification, characterization, and cloning of a eubacterial 3-hydroxy-3-methylglutaryl coenzyme A reductase, a key enzyme involved in biosynthesis of terpenoids.

Authors:  S Takahashi; T Kuzuyama; H Seto
Journal:  J Bacteriol       Date:  1999-02       Impact factor: 3.490

9.  Characterization of the Mycobacterium tuberculosis 4-diphosphocytidyl-2-C-methyl-D-erythritol synthase: potential for drug development.

Authors:  Hyungjin Eoh; Amanda C Brown; Lori Buetow; William N Hunter; Tanya Parish; Devinder Kaur; Patrick J Brennan; Dean C Crick
Journal:  J Bacteriol       Date:  2007-10-05       Impact factor: 3.490

10.  Structure of (E)-4-hydroxy-3-methyl-but-2-enyl diphosphate reductase, the terminal enzyme of the non-mevalonate pathway.

Authors:  Ingo Rekittke; Jochen Wiesner; Rene Röhrich; Ulrike Demmer; Eberhard Warkentin; Weiya Xu; Kathrin Troschke; Martin Hintz; Joo Hwan No; Evert C Duin; Eric Oldfield; Hassan Jomaa; Ulrich Ermler
Journal:  J Am Chem Soc       Date:  2008-12-24       Impact factor: 15.419

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.