Table 3.

Secondary metabolites biosynthesized by B. halotolerans Cal.l.30 and putatively annotated through UHPLC-HRMS analysis.

Antibiotic Compounds	Molecular Formula	Experimental m/z	RT (min)	Δppm	Adduct	Reference or Source
Mojavensin A	C₅₀H₇₇N₁₃O₁₄	1082.5617	14.66	-1.13	[M–H]-	[49]
Surfactin A C₁₃	C₅₁H₈₉N₇O₁₃	1006.6447	22.699	1.23	[M–H]-	[50]
Surfactin A C₁₅	C₅₃H₉₃N₇O₁₃	1035.683	23.945	0.57	[M–H]-	[51]
Fengycin A C₁₆	C₇₂H₁₁₀N₁₂O₂₀	1461.7893	16.51	1.19	[M–H]-	[52]
Bacillaene A	C₃₄H₄₈N₂O₆	579.3441	16.365	2.13	[M–H]-	[53]
dihydrobacillaene A	C₃₄H₅₀N₂O₆	581.3597	16.24	2.04	[M–H]-	[53]
Bacillaene B	C₄₀H₅₈N₂O₁₁	741.3978	14.357	2.85	[M–H]-	[54]
Bacillaene C	C₄₄H₆₄N₂O₁₄	843.4293	14.984	2.27	[M–H]-	[54]
L-dihydroanticapsin	C₉H₁₅NO₄	200.0923	11.395	2.83	[M–H]-	[55]
Azelaic acid	C₉H₁₆O₄	187.0969	11.022	2.21	[M–H]-	[56]
Bacillibactin	C₃₉H₄₂N₆O₁₈	881.2497	11.88	2.85	[M–H]-	[57]
15-hydroxypentadecanoid acid	C₁₅H₃₀O₃	257.2124	17.953	4.97	[M–H]-	[58]
2-hydroxyphenylacetic acid	C₈H₈O₃	151.0391	9.381	0.86	[M–H]-	[59]