Category:Team Proteocritics

Fig. 3: It was found that DhlA is highly expressed in strains lacking dehalogenase activity and strains with impaired dicholoethane utilization abilities.

Fig. 3A/3C shows that 4-hydroxylaminobenzoate is converted to PCA in cells with overexpressed PnbB.

Fig. 3A/3B shows that in cells containing overexpressed PnbA, 4NBen is converted to 4-hydroxylaminobenzoate in the presence of NADH.

Fig. 2 indicates that 2-AMS was converted to 2-aminomuconate by AmnC. An absorbance maxima appears at A326 instead of A263 when AmnC is included.

Figure 10: Shows that the recombinant E.coli XL1-Blue strains with vdh gene converted vanillin to vanillic acid.

Figure 4B: Shows that ligV-inactivation mutant (DLV) did not have significant growth on vanillin, yet the wild-type strain SYK-6 did have significant growth on vanillin

Table 1: Shows that culture crude protein extracts demonstrated caffeic acid O-methyltransferase activity.

Figure 2: Shows that when the RsCAS gene was introduced into yeast, cycloartenols were produced

Table 2: Shows that a mutant strain MD186 (affecting the glcK gene) has complete loss of glucose kinase activity

Figure 2: Shows that the inhibition of 2-oxoglutarate-dependent dioxygenases significantly decreases the production of DIMBOA

Figure 4: Shows that the RhAAT1 gene product catalyzed the production of geranyl acetate from gerniol and aceyl-CoA and that this was dependent on the presence of the RhAAT1 gene product (enzyme).

Table 2. Mutants of the purU gene, along with the wild-type strains of E.coli were grown on medium containing various amino acids. Mutants required purine or formate supplementation for growth indicating role of purU in de novo purine nucleotide biosynthesis.

Figure 2B shows that in cells containing both abiQ and antiQ, antiQ RNA is cleaved resulting in multiple bands on agarose gel.