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. 2018 May 4;9:829. doi: 10.3389/fmicb.2018.00829

Table 3.

In vitro antagonistic activities of the three BCA candidates against Lasiodiplodia theobromae.

Activities BCA1 BCA2 BCA3
Production of diffusible metabolites using the cup plate technique (diameter of zone of inhibition measured in mm) 67.97 ± 0.91 a 53.82 ± 0.93 b 0.00 ± 0.00 c
Production of diffusible metabolites using the dialysis membrane technique from the fish meal extract agar platesa + +
Production of chitinase using the dialysis membrane technique from the colloidal chitin agar platesa + +
Production of volatile compoundsa +
Production of hydrogen cyanideb
Production of siderophoresb +
Chitinase from colloidal chitin (U ml−1)c 5.56 ± 0.17 a 0.00 ± 0.00 b 7.75 ± 0.22 c
Chitinase from L. theobromae cell wall (U ml−1)c 3.73 ± 0.14 a 0.00 ± 0.00 b 5.60 ± 0.21 c
ß-1,3-glucanase from laminarin (U ml−1)d 3.57 ± 0.16 a 0.00 ± 0.00 b 5.54 ± 0.18 c
ß-1,3-glucanase from L. theobromae cell wall (U ml−1)d 2.79 ± 0.20 a 0.00 ± 0.00 b 3.76 ± 0.21 c
a

+, fungicidal effect; −, no fungicidal effect.

b

+, produced; −, not produced.

c

A unit of chitinase was expressed as the amount of the enzyme that released 1 μmol of N-acetyl-D-glucosamine mg−1 protein h−1.

d

A unit of ß-1,3-glucanase was expressed as the amount of the enzyme that released 1 μmol of glucose mg−1 protein h−1.

Values are means of three replicates ± SE. Values with the same letter within a row are not significantly (P > 0.05) different according to Duncan's multiple range test.

BCA1, isolate #12; Streptomyces samsunensis UAE1; BCA2, isolate #29; S. cavourensis UAE1; BCA3, isolate #44; Micromonospora tulbaghiae UAE1.