A Common Genetic Determinant of Xanthine Dehydrogenase and Nitrate Reductase in Nicotiana tabacum

1976 ◽  
Vol 170 (6) ◽  
pp. 538-541 ◽  
Author(s):  
Ralf-R. Mendel ◽  
Andreas J. Müller
1982 ◽  
Vol 105 (3) ◽  
pp. 219-227 ◽  
Author(s):  
D. Pental ◽  
S. Cooper-Bland ◽  
K. Harding ◽  
E.C. Cocking ◽  
A.J. Müller

1970 ◽  
Vol 16 (2) ◽  
pp. 151-163 ◽  
Author(s):  
C. M. Lewis ◽  
J. R. S. Fincham

SUMMARYMutants ofUstilago maydishave been isolated both, deficient and derepressed for nitrate reduction. Those deficient in enzyme fall into six groups, one of which is the structural gene. Enzyme which has proved to be more labile than that of wild-type has been isolated from a temperature-sensitive mutant at this locus. All the mutants in the structural gene have xanthine dehydrogenase activity and the situation closely parallels that ofAspergillus nidulans.The derepressed mutants fall into four complementation groups and all are partially derepressed in that they are further inducible by nitrate. Full derepression can be conferred by induction of a second mutation. In one analysed case the second reinforcing mutation proved to be pheno-typically similar to the first one when separated from it.


1991 ◽  
Vol 278 (2) ◽  
pp. 393-397 ◽  
Author(s):  
H N Truong ◽  
C Meyer ◽  
F Daniel-Vedele

Tobacco nitrate reductase (NR) produced in yeast retains cytochrome c reductase activity, but not NR activity. Biochemical data suggest that the haem and FAD domains are functional, and that the molybdenum cofactor (MoCo) domain is inactive owing to the absence of MoCo in yeast. The native form of the produced NR is dimeric. Thus MoCo is not involved in NR dimerization in higher plants, contrary to current assumptions.


Genetics ◽  
1980 ◽  
Vol 95 (3) ◽  
pp. 649-660
Author(s):  
A Brian Tomsett ◽  
Reginald H Garrett

ABSTRACT The isolation and characterization of mutants altered for nitrate assimilation in Neurospora crassa is described, The mutants isolated can be subdivided into five classes on the basis of growth tests that correspond to the growth patterns of existing mutants at six distinct loci. Mutants with growth characteristics like those of nit-2, nit-3 and nit-6 are assigned to those loci on the basis of noncomplementation and lack of recombination. Mutants that, from their growth patterns, appear to lack the molybdenum-containing cofactor for both nitrate reductase and xanthine dehydrogenase subdivide into three loci (nit-7, nit4 and nit-9), all of which are genetically distinct from nit-1. nit-9 is a complex locus consisting of three complementation groups and thus appears similar to the cnxABC locus of Asperillus nidulans. Extensive complementational and recombinational analyses reveal that nit-4 and nit-5 are alleles of the same locus, and two new alleles of that locus have been isolated. The results indicate that, as in A. nidulans, nitrate assimilation in N. crassa requires at least four loci (nit-1,7,8 and 9) to produce the molybdenum co-factor for nitrate reductase (and xanthine dehydrogenase), one locus (nit-3) to code for the nitrate reductase apoprotein, one locus (nit-6) to code for the nitrite reductase approtein and only one locus (nit-4/5) for the regulation of induction of the pathway by nitrate and nitrite.


1978 ◽  
Vol 44 (3) ◽  
pp. 273-277 ◽  
Author(s):  
KRISTINA GLIMELIUS ◽  
TAGE ERIKSSON ◽  
REINHARD GRAFE ◽  
ANDREAS J. MULLER

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