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The activity of ASNase II was assayed using the Nessler method [20].
MnP activity was assayed using the method described by Paszczyński et al. (1988).
SOD activity was assayed using the xanthine xanthine oxidase and nitroblue tetrazolium (NBT) system.
Hydrogen peroxide (H2O2) content was assayed using the method by Moloi and van der Westhuizen (2006).
LiP activity was assayed using the method described by Tien and Kirk (1988).
The activity of the entrapped enzyme was assayed using the Sigma lipase activity method.
Cytochrome c oxidase (CcO) was assayed using the kit for bacteria (Genmed Scientifics Inc., Wilmington, DE, USA).
Tissue protein was assayed using the Bio-Rad kit (Bio-Rad Laboratories, HerCAles, Cagaingain using the manufacturer's protocols.
The plate was assayed using the FP assay above.
The stability of the members of the actinome was assayed using the algorithm PESTfind [36], [37].
Protein concentration was assayed using the Bio-Rad DC kit (Bio-Rad, Hercules, CA).
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