Category:Team The Microbial Produced Beverages

Table 2 shows that PilA specifically hydrolyzes GTP

Figure 3 shows a reduction in nitroreductase activity in mutant phenotypes linked to alterations in nsfB

Table 2 shows an enzyme assay used in order to demonstrate Glutamate-cysteine ligase formation from GshF

Fig. 2 shows maleamate hydrolysis activity

Fig. 2A: Frog oocytes injected with human ZIP4 mRNA showed significant zinc ion uptake activity compared to a negative control.

Figure 3 shows that the mutant phenotype was unable to hydrolyze phosphate off phosphatidylinositol 4,5-bisphosphate

Figure 3 shows an enzyme assay of 3′-amino-3′-dATP pyrophosphohydrolase activity by pur7

Figure 3 shows a mutation in which no sulfolipid production was detected.

Figure 3 shows an enzyme assay for the GTPase activity of FtsZ

Fig. 6: E. coli transformed with GGTBP show gamma-glutamyltransferase activity using many different amino acids acceptors.

Fig. 10: the four ODC mutants show significantly reduced enzyme activity compared to the wild type ODC.

Fig. 5: pH-rate profile for synthesis of PDC shows hydrolase activity of LigI.

Table 1: enzyme assay shows L-rhamnose activity

Fig. 4: The expression of motility genes fliA, flhC and flhD genes are reduced in rpoN mutants compared to wild type E. coli.

Figure 4A shows the transformation frequency was greater in the rpoS+ strain than in the rpoS- strain at similar optimal culture densities.

Figure 3D. Results indicate EF-Tu was degraded faster in the hslO deletion strain than in wild-type cells. Hsp33 protects EF-Tu against protein

degradation by acting as a chaperone.