Literature DB >> 33665688

Underground metabolism facilitates the evolution of novel pathways for vitamin B6 biosynthesis.

Björn Richts1, Fabian M Commichau2.   

Abstract

The term vitamin B6 is a designation for the vitamers pyridoxal, pyridoxamine, pyridoxine and the respective phosphate esters pyridoxal-5'-phosphate (PLP), pyridoxamine-5'-phosphate and pyridoxine-5'-phosphate. Animals and humans are unable to synthesise vitamin B6. These organisms have to take up vitamin B6 with their diet. Therefore, vitamin B6 is of commercial interest as a food additive and for applications in the pharmaceutical industry. As yet, two naturally occurring routes for de novo synthesis of PLP are known. Both routes have been genetically engineered to obtain bacteria overproducing vitamin B6. Still, major genetic engineering efforts using the existing pathways are required for developing fermentation processes that could outcompete the chemical synthesis of vitamin B6. Recent suppressor screens using mutants of the Gram-negative and Gram-positive model bacteria Escherichia coli and Bacillus subtilis, respectively, carrying mutations in the native pathways or heterologous genes uncovered novel routes for PLP biosynthesis. These pathways consist of promiscuous enzymes and enzymes that are already involved in vitamin B6 biosynthesis. Thus, E. coli and B. subtilis contain multiple promiscuous enzymes causing a so-called underground metabolism allowing the bacteria to bypass disrupted vitamin B6 biosynthetic pathways. The suppressor screens also show the genomic plasticity of the bacteria to suppress a genetic lesion. We discuss the potential of the serendipitous pathways to serve as a starting point for the development of bacteria overproducing vitamin B6. KEY POINTS: • Known vitamin B6 routes have been genetically engineered. • Underground metabolism facilitates the emergence of novel vitamin B6 biosynthetic pathways. • These pathways may be suitable to engineer bacteria overproducing vitamin B6.

Entities:  

Keywords:  Enzyme promiscuity; Enzyme specificity; Genetic suppression; Promiscuous enzyme; Pyridoxal 5′-phosphate

Mesh:

Substances:

Year:  2021        PMID: 33665688      PMCID: PMC7954711          DOI: 10.1007/s00253-021-11199-w

Source DB:  PubMed          Journal:  Appl Microbiol Biotechnol        ISSN: 0175-7598            Impact factor:   4.813


  81 in total

1.  Inhibitory cross-talk upon introduction of a new metabolic pathway into an existing metabolic network.

Authors:  Juhan Kim; Shelley D Copley
Journal:  Proc Natl Acad Sci U S A       Date:  2012-09-14       Impact factor: 11.205

2.  Assignment of function to a domain of unknown function: DUF1537 is a new kinase family in catabolic pathways for acid sugars.

Authors:  Xinshuai Zhang; Michael S Carter; Matthew W Vetting; Brian San Francisco; Suwen Zhao; Nawar F Al-Obaidi; Jose O Solbiati; Jennifer J Thiaville; Valérie de Crécy-Lagard; Matthew P Jacobson; Steven C Almo; John A Gerlt
Journal:  Proc Natl Acad Sci U S A       Date:  2016-07-11       Impact factor: 11.205

3.  Studies on cyanobacterial protein PipY shed light on structure, potential functions, and vitamin B6 -dependent epilepsy.

Authors:  Lorena Tremiño; Alicia Forcada-Nadal; Asunción Contreras; Vicente Rubio
Journal:  FEBS Lett       Date:  2017-09-20       Impact factor: 4.124

Review 4.  Phylogenetic analyses and comparative genomics of vitamin B6 (pyridoxine) and pyridoxal phosphate biosynthesis pathways.

Authors:  G Mittenhuber
Journal:  J Mol Microbiol Biotechnol       Date:  2001-01

5.  On the two components of pyridoxal 5'-phosphate synthase from Bacillus subtilis.

Authors:  Thomas Raschle; Nikolaus Amrhein; Teresa B Fitzpatrick
Journal:  J Biol Chem       Date:  2005-07-19       Impact factor: 5.157

Review 6.  Two independent routes of de novo vitamin B6 biosynthesis: not that different after all.

Authors:  Teresa B Fitzpatrick; Nikolaus Amrhein; Barbara Kappes; Peter Macheroux; Ivo Tews; Thomas Raschle
Journal:  Biochem J       Date:  2007-10-01       Impact factor: 3.857

7.  Structural genes for thiamine biosynthetic enzymes (thiCEFGH) in Escherichia coli K-12.

Authors:  P B Vander Horn; A D Backstrom; V Stewart; T P Begley
Journal:  J Bacteriol       Date:  1993-02       Impact factor: 3.490

Review 8.  A history of the isolation and identification of vitamin B(6).

Authors:  Irwin H Rosenberg
Journal:  Ann Nutr Metab       Date:  2012-11-26       Impact factor: 3.374

9.  Higher-order epistasis shapes the fitness landscape of a xenobiotic-degrading enzyme.

Authors:  Gloria Yang; Dave W Anderson; Florian Baier; Elias Dohmen; Nansook Hong; Paul D Carr; Shina Caroline Lynn Kamerlin; Colin J Jackson; Erich Bornberg-Bauer; Nobuhiko Tokuriki
Journal:  Nat Chem Biol       Date:  2019-10-21       Impact factor: 15.040

10.  Metabolism gets lucky.

Authors:  Tim F Cooper
Journal:  Mol Syst Biol       Date:  2010-11-30       Impact factor: 11.429

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