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The categories of translation, replication, nucleotide transport, posttranslational modification and cell wall processes are overrepresented in our gene set compared to both total and normalised gene distribution in the COG database.
An examination of the distribution of these ancestral pseudogenes by functional group shows that CDS belonging to one specific group, "cell wall and cell wall processes", are significantly overrepresented (35%, compared with ~22% for all CDS in M. marinum M and M. ulcerans Agy99).
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A variety of other proteins from multiple functional families including intermediary metabolism and respiration, lipid metabolism, and cell wall processes were also identified.
More specifically, defining the role of specific cellulose syntheses in so far as their specificity for either primary or secondary cell wall processes is relevant to understanding elongation.
However, much of our data using Li 1 in a DP5690 genetic background suggested that molecular events involved in cellulose deposition and secondary cell wall synthesis were not affected to the degree that primary cell wall processes were.
In addition to transcripts negatively affecting cell proliferation, a large number of genes related to cell wall modifying processes are upregulated in adaxial petals.
Cell-wall remodeling processes are tightly regulated to warrant bacterial survival and in some cases are directly linked to antibiotic resistance.
Interestingly, numerous transcripts associated with cell wall related processes were repressed, e.g., pectinesterase (DMP400009250), polygalactouranase (DMP400023907), glycine rich cell wall protein (DMP400050455), chitin binding lectin (DMP400055565) and β-1-3 glucan synthase (DMP400049943).
Three configurations, including the conventional extractive distillation (CED), extractive distillation under reduced pressure (EDRP) and extractive dividing-wall column (EDWC) processes are investigated in order to obtain the optimal separation configurations.
These results support that cell wall morphogenetic processes were affected by myosin II deficiency.
After 11 h of phosphite treatment a much more pronounced effect on several cell wall modification processes was observed.
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