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Climate changes are affecting the plant production, including sugar beet growing especially in the southern and central parts of the Europe. Modifying the sowing and harvesting dates are one of the most often used adaptations in sugar beet cultivation. The aim of this study was to assess the interactions between planting date and sugar beet genotypes for different harvest dates with recommendation for duration of vegetation period for specific hybrids in order to achieve the best performance and to evaluate influence of climatic factors on sugar yield. Three-way analysis of variance and AMMI (Additive main effect and multiple interactions) analysis were performed to investigate interaction between main factors. Analysis of variance revealed that genotypes (G), planting date (PD), harvest date (HD) and interaction G × PD significantly affected sugar yield in 2016. In 2017 genotypes, planting date, harvest date and G x PD interaction significantly affected sugar yield on probability level of 1%, while PD × HD interaction had significant effect on probability level of 5%. Results of AMMI analysis enabled discrimination of genotypes with the highest level of stability in certain planting dates. Hybrids with combined yield and sugar content (NZ type) should have the advantage in earlier planting dates compared to of sugar beet hybrids with higher sugar content (Z type). However, in shortened vegetation period Z type hybrids are more stable and with better sugar yield results. Results of our study suggest that delaying the harvest date decreases differences between sugar yields obtained from hybrids sown in different planting dates. Major factors in the study affecting sugar yield were growing degree days, insolation and number of days from planting to harvest.

Microbial surface and secreted proteins (the secretome) contain a large number of proteins that interact with other microbes, host and/or environment. These proteins are exported by the coordinated activities of the protein secretion machinery present in the cell. A group of bacteriophage, called filamentous phage, have the ability to hijack bacterial protein secretion machinery in order to amplify and assemble via a secretion-like process. This ability has been harnessed in the use of filamentous phage of Escherichia coli in biotechnology applications, including screening large libraries of variants for binding to "bait" of interest, from tissues in vivo to pure proteins or even inorganic substrates. In this review we discuss the roles of secretome proteins in pathogenic and non-pathogenic bacteria and corresponding secretion pathways. We describe the basics of phage display technology and its variants applied to discovery of bacterial proteins that are implicated in colonization of host tissues and pathogenesis, as well as vaccine candidates through filamentous phage display library screening. Secretome selection aided by next-generation sequence analysis was successfully applied for selective display of the secretome at a microbial community scale, the latter revealing the richness of secretome functions of interest and surprising versatility in filamentous phage display of secretome proteins from large number of Gram-negative as well as Gram-positive bacteria and archaea.