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At 37°C, the protein bands of wild type and mutant were of equal width (Fig. 7b, lanes 1, 2) whereas the mutant was higher than wild type 42°C (Fig. 7b, lanes 3, 4).
Considering the proximity of Asn155 to the essential heme iron ligand of HCCS (His154), the heme-binding properties of this mutant were of particular interest.
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The mutant is of potential interest for industrial applications.
As shown in Figure 7H and 7I, contraction of the basal complex in this mutant was of lower efficiency.
The mutants of spl, ems1 are of L er background as described [ 22, 32], while the ams mutant is of Columbia background.
With respect to structure-based predictions the results with the R70Q IRAK-M mutant are of major importance.
Minute mutants were of the genotypes y[1] w; P[w[+mC]=lacW]RpS13 /CyO and P[lacW]RpL36 G0471 w 67c23/FM7a.
Such mutants are of great interest in overcoming the increasing danger of antibiotic resistance.
Another repeat-associated change in phage 812-derived mutants is of the copy number of tandem repeats in the variable right terminus as a characteristic feature of Kayvirus genomes, which probably plays a significant role in replication and packaging35.
In addition, bloodstream forms of the mutant were capable of differentiating to the procyclic form without a detectable growth phenotype.
The enhanced activities from those treated GCase mutant were ≥35% of the WT level.
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