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J Power

Publications and source records attributed to J Power.

30 records · Page 2Linked to original sources

L-arabinose isomerase formation in a conditional mutant of gene araA of Escherichia coli B-r.

A temperature-sensitive mutant of Escherichia coli in which the synthesis of l-arabinose isomerase is blocked during growth at 42 C was found to possess the following properties. (i) The mutation occurred in the structural gene for the isomerase, gene araA. (ii) During growth at elevated temperatures the mutant accumulates a product which is a precursor to the active enzyme. (iii) The precursor produced at 42 C is slowly converted to active enzyme at 28 C in the absence of protein and ribonucleic acid synthesis. It is concluded that the mutation results in a change in the structure of isomerase which causes formation of active enzyme to be thermolabile at a step beyond the level of translation.

Arabinose

Positive control of enzyme synthesis by gene C in the L-arabinose system.

Englesberg, Ellis (University of Pittsburgh, Pittsburgh, Pa.), Joseph Irr, Joseph Power, and Nancy Lee. Positive control of enzyme synthesis by gene C in the l-arabinose system. J. Bacteriol 90:946-957. 1965.-The l-arabinose gene complex consists of genes D, A, B, and C, linked in that order between the markers thr and leu, and an unlinked gene E. Genes D, A, B, and E are the structural genes for three inducible enzymes and permease, respectively. Gene C, with two mutant alleles, C(-) and C(c), is the regulatory gene exhibiting positive and negative control. C(-) mutants are deficient and C(c) mutants are constitutive for all three enzymes and permease. Complementation analysis, employing sexual merozygotes (A(-)C(+) x A(+)C(-)), with six different C(-) mutants, demonstrates that C(-) is recessive to C(+) (positive control). A total of 61 C(c) mutants, isolated as clones resistant to d-fucose inhibition, are linked to the leu ara region of the chromosome, and the 22 C(c) mutants that were analyzed in detail mapped within the C gene among the C(-) mutant sites. C(c) mutants produce various but coordinate levels of the two enzymes measured, and permease. Complementation analysis (A(-)C(c) x A(+)C(-), A(-)C(c) x A(+)C(+)) shows that C(c) is dominant to C(-) (positive control) and recessive to C(+) (negative control). Deletion mutants that extend into the C gene are l-arabinose permease-negative, thus supporting the positive regulatory role of the C gene. The name "activator gene" is proposed for genes of the C type to accentuate their positive role in gene expression. A working model consistent with these results is presented.

Arabinose

Reappraisal of the genetic map of Chlamydomonas reinhardtii.

In Chlamydomonas reinhardtii, we have found that linkage groups XII and XIII define only a single linkage group and that linkage groups XVI and XVII also define a single linkage group. The interdigitation of the genetic maps of linkage groups XII and XIII and of XVI and XVII is presented. At present, 17 linkage groups that display Mendelian segregation have been identified in C. reinhardtii.

Chlamydomonas