Fungi of the genus Fusarium are economically significant pathogens in most wheat-growing regions worldwide. The biocontrol agents Bacillus velezensis BZR 336 g and BZR 517 were tested for growth inhibition of F. graminearum BZR 4. The results demonstrated that the strains are capable of deforming and destroying hyphae. The modified bioautography technique showed that the strains produce iturin A and surfactin, which probably explains the mechanism of pathogen inhibition. Furthermore, lipopeptides were detected and identified in two samples by the HPLC-HRMS. Compounds such as surfactin and their isomers and homologues were found in both samples. An experiment on an artificial infectious background in a climatic chamber established that the biological effectiveness of strains is close to that of chemical and biological references. Cultivation of plants with B. velezensis showed that the strains are likely to reduce the stress load. An efficacy of up to 45.0% was determined for bioagents BZR 336 g and BZR 517 in field trials, while the yield was up to 7.9 t/ha. The use of B. velezensis BZR 336 g and BZR 517 as biocontrol agents provides an environmentally friendly approach to the control of Fusarium rots on wheat, reduction of the pesticide load, and hence quality harvest.

Mono- and polysaccharides are an essential part of every biological system. Identifying underivatized carbohydrates using mass spectrometry is still a challenge because carbohydrates have a low capacity for ionization. Normally, the intensities of protonated carbohydrates are relatively low, and in order to increase the corresponding peak height, researchers add Na⁺, K⁺, or NH₄⁺to the solution. However, the fragmentation spectra of the corresponding ions are very poor. Based on this, reliably identifying carbohydrates in complex natural and biological objects can benefit frommeasuring additional molecular descriptors, especially those directly connected to the molecular structure. Previously, we reported that the application of the isotope exchange approach (H/D and ¹⁶O/¹⁸O) to high-resolution mass spectrometry can increase the reliability of identifying drug-like compounds. Carbohydrates possess many –OH and –COOH groups, making it reasonable to expect that the isotope exchange approach would have considerable potential for detecting carbohydrates. Here, we used a collection of standard carbohydrates to investigate the isotope exchange reaction (H/D and ¹⁶O/¹⁸O) in carbohydrates and estimate its analytical applications.