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An Embryo-Defective Mutant of Arabidopsis Disrupted in the Final
Step of Biotin Synthesis
David A. Patton,
Amy L. Schetter,
Linda H. Franzmann,
Karin Nelson,
Eric R. Ward, and
David W. Meinke*
Novartis Crop Protection, P.O. Box 12257, Research Triangle Park,
North Carolina 27709 (D.A.P., K.N., E.R.W.); and Department
of Botany, Oklahoma State University, Stillwater, Oklahoma 74078 (A.L.S., L.H.F., D.W.M.)
Auxotrophic mutants have played an
important role in the genetic dissection of biosynthetic pathways
in microorganisms. Equivalent mutants have been more difficult to
identify in plants. The bio1 auxotroph of
Arabidopsis thaliana was shown previously to be
defective in the synthesis of the biotin precursor
7,8-diaminopelargonic acid. A second biotin auxotroph of A. thaliana has now been identified. Arrested embryos from this
bio2 mutant are defective in the final step of biotin
synthesis, the conversion of dethiobiotin to biotin. This enzymatic
reaction, catalyzed by the bioB product (biotin synthase) in Escherichia coli, has been studied
extensively in plants and bacteria because it involves the unusual
addition of sulfur to form a thiophene ring. Three lines of evidence
indicate that bio2 is defective in biotin synthase
production: mutant embryos are rescued by biotin but not dethiobiotin,
the mutant allele maps to the same chromosomal location as the cloned
biotin synthase gene, and gel-blot hybridizations and polymerase chain
reaction amplifications revealed that homozygous mutant plants contain a deletion spanning the entire BIO2-coding region. Here
we describe how the isolation and characterization of this null allele
have provided valuable insights into biotin synthesis, auxotrophy, and
gene redundancy in plants.
*
Corresponding author; e-mail
meinke{at}osuunx.ucc.okstate.edu; fax
1-405-744-7074.
Plant Physiol. (1998) 116: 935-946
Copyright Clearance Center: 0032-0889/98/116/0935/12
© 1998 American Society of Plant Physiologists
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