Table 2 Antimicrobial compounds produced by the selected dark septate endophytic (DSE) fungal isolates APDS 3.2, TBMDS 2.4b, and TMDS 3.2
No | Name of the compound | Molecular formula | Origin compound | Compound content (%) | Ref | ||
|---|---|---|---|---|---|---|---|
APDS 3.2 | TBMDS 2.4b | TMDS 3.2 | |||||
1 | Acetic acid butyl methyl-phosphinoylmethyl ester | C8H17O3P | Ester | 30.76 | 25.06 | 29.14 | Siddiquee (2014) |
2 | Dimethyl sulfoxide | C2H6OS | Organosulfur compounds | 11.38 | – | 10.06 | Sanmartín-Suárez et al. (2011) |
3 | Benzenemethanol, 3,5-dimethyl- | C9H12O | Alcohol | 5.13 | – | – | Ma et al. (2012) |
4 | 1,5,6,7-Tetramethylbicyclo |3.2.0| hepta-2,6-diene | C11H16 | Alcohol | 1.40 | – | 1.37 | Wang et al. (2018) |
5 | Ethanone, 1-(4-methyl-1H-imidazol-2-yl)- | C6H8N2O | Azol | 3.55 | 2.87 | 3.30 | Akter et al. (2018) |
6 | Ethanimidic acid, 2-cyclohexylidene-N-phenyl-methyl ester | C15H19NO | Carboxylic acid | 1.57 | – | 1.39 | Saladino et al. (2011) |
7 | Boric Acid | H3BO3 | DMSO | 1.16 | 1.16 | – | Rolshausen & Gubler (2005) |
8 | Triethylsilanol | C6H16OSi | Organic silanol | – | 1.30 | – | Yun-mi et al. (2006) |
9 | l-Norvaline | C5H11NO2 | Amino acids | – | 1.04 | 1.30 | Samardzic and Rodgers (2019) |
10 | Palmitic acid | C16H32O2 | Carboxylic acid | – | 1.94 | – | Liu et al. (2008) |
11 | 11-Octadecenoic acid | C18H34O2 | methyl ester | – | 2.35 | – | Reis et al. (2019) |
12 | i-Propyl 9-octadecenoate | C21H40O2 | Propyl Ester | – | 1.74 | – | Reis et al. (2019) |
13 | Tricosane | C23H48 | Alkane | – | 2.32 | – | Tao et al. (2018) |
14 | i-Propyl 11,12-methylene octadecenoate | C22H42O2 | Ester | – | 2.22 | – | Tang et al. (2016) |
15 | 2-Carene | C10H16 | Monoterpene hydrocarbon | – | – | 7.55 | Teixeira et al. (2013) |