Category:Team ttKtt

Figure 3 depicts the optimum temperature and pH for endochitinase activity.

Table 2 depicts kinetic parameters of both the wild-type and mutant M. fervidus GraP-DHs.

Figure 3 shows the inhibition of both the alternative and classical pathways of complement activation through the inhibition of complement-mediated hemolysis of rabbit erthrocytes.

Figure 5 demonstrates the activity of Zn(II) and Co(II) trzN with selected s-triazines as substrates.

Figure 4 shows the effect of metal addition on ametryn hydrolysis activity of native TrzN purified from recombinant cells grown on 500M zinc and metal-depleted TrzN.

Table 2 depicts the HmADH12 gene followed Michaelis–Menten kinetics with the acetaldehyde substrate and NADP+ and NADPH cofactors in the reductive reaction. The enzyme was positively co-operative with ethanol as a substrate in the oxidative reaction.

Figure 3 demonstrates the ability for the mutant to grow on media with minimal or saturated B12.

Figure 6 shows that PduQ regenerates NAD+ for the PduP reaction in purified Pdu MCPs by demonstrating the concentration of propionyl-CoA in comparison with a mutant phenotype.

Figure 3 demonstrates the rgtA activity through its ability to be a galA donor and viewing the total lipid extracts from strains with the enzyme vs. strains without the enzyme

Figure 5 depicts the ability of the ABC transporter, peptide-binding protein to reduce U(VI) in T. scotoductus SA-01. The reduction levels in the mutants with the protein was plotted against the reduction levels in the protein-free controls.

Figure 3 depicts oxygen-limited fermentation tests using the xylA mutants. Ethanol production was only present in the second- and third- round mutants, and xylose consumption was increased in these strains.

Table 2 depicts the wild-type xylose isomerase gene from Piromyces sp. and the first-, second-, and third-round mutants expressed in S. cerevisiae. In vitro xylose isomerase activity was measured and reported.

Figure 3 demonstrates the inhibitory activities on MurA and then determines the residual activity.

Figure 5 demonstrates the inhibitory actions of sulfhydryl group dependent activity on the mutant phenotype.