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. 2022 Jul 18;11(14):1872. doi: 10.3390/plants11141872

Table 2.

Extracellular hydrolytic enzymes produced by the tested Actinomycetes isolates.

Enzyme Substrates Staining Diameter of Hydrolysis Area (mm)
AC1
Streptomyces sp.
RS3
S. atratus
OL2
A. humicola
Chitinase Chitin azure (1%) Congo red (0.03%) 23.0 ± 2.3 b 0.0 ± 0.0 c 31.5 ± 1.7 a
Chitin crab shells (1%) Congo red (0.03%) 0.0 ± 0.0 0.0 ± 0.0 0.0 ± 0.0
Amylase Soluble starch (1%) Lugol solution (a) 37.5 ± 2.9 a 42.0 ± 1.2 a 28.0 ± 3.5 b
Glucanase Lichenan (0.2%) Congo red (0.03%) 22.0 ± 2.3 b 0.0 ± 0.0 c 36.0 ± 1.2 a
Pectinase Pectin (0.5%) CTAB (b) (2%) 14.0 ± 1.2 a 10.5 ± 1.7 a 0.0 ± 0.00 b
Protease Skim milk (1%) - 14.5 ± 2.9 b 12.5 ± 2.9 b 21.5 ± 1.7 a
Polygalacturanase Polygalacturonic acid (1%) Ruthenium red (0.1%) 0.0 ± 0.0 0.0 ± 0.0 0.0 ± 0.0

(a) Lugol solution was prepared as follows: 0.35 g iodide + 0.66 g potassium iodide KI in 100 mL dis. H2O; (b) CTAB: hexadecyltrimethylammonium bromide; values followed by different letters in each row for each tested enzyme were significantly different according to Tukey’s B multiple comparison test post hoc test at p < 0.05.