Abstract
In this paper we describe the isolation of a second gene in the newly identified pyridoxine biosynthesis pathway of archaebacteria, some eubacteria, fungi, and plants. Although pyridoxine biosynthesis has been thoroughly examined in Escherichia coli, recent characterization of the Cercospora nicotianae biosynthesis gene PDX1 led to the discovery that most organisms contain a pyridoxine synthesis gene not found in E. coli. PDX2 was isolated by a degenerate primer strategy based on conserved sequences of a gene specific to PDX1-containing organisms. The role of PDX2 in pyridoxine biosynthesis was confirmed by complementation of two C. nicotianae pyridoxine auxotrophs not mutant in PDX1. Also, targeted gene replacement of PDX2 in C. nicotianae results in pyridoxine auxotrophy. Comparable to PDX1, PDX2 homologues are not found in any of the organisms with homologues to the E. coli pyridoxine genes, but are found in the same archaebacteria, eubacteria, fungi, and plants that contain PDX1 homologues. PDX2 proteins are less well conserved than their PDX1 counterparts but contain several protein motifs that are conserved throughout all PDX2 proteins.
MeSH Terms
Amino Acid Sequence
Archaeal Proteins/genetics,metabolism
Ascomycota/genetics,metabolism
Bacillus subtilis/genetics,metabolism
Bacterial Proteins/genetics,metabolism
Base Sequence
Fungal Proteins/genetics,isolation & purification,metabolism
Gene Targeting
Genetic Complementation Test
Molecular Sequence Data
Mutation
Mycobacterium leprae/genetics,metabolism
Plant Proteins/chemistry,genetics,metabolism
Pyridoxine/biosynthesis,genetics
Pyrococcus/genetics,metabolism
Sequence Analysis, DNA
Sulfolobus/genetics,metabolism
Transformation, Genetic
Triticum/genetics,metabolism
Chemicals
Archaeal Proteins
Bacterial Proteins
Fungal Proteins
PDX2 protein, Cercospora nicotianae
Plant Proteins
Pyridoxine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Ehrenshaft M
Department of Plant Pathology, North Carolina State University, Raleigh, NC 27695, USA. mel@unity.ncsu.edu
Daub M E
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