Electron-microscopic studies were carried out on S and R variants of Brucella suis 1330 and the production of L forms induced with the use of penicillin. No variations were established in the ultrastructure of the initial forms. However, essential differences were observed in the ultrastructure between the latter and the L-transformed Brucellae as well as changes that differentiated the ultrastructure of L forms obtained from S variants from that of L forms obtained from R variants. In both cases the L-transformed Brucella organisms have suffered substantial changes in their electron-microscopic structure. There was no cell wall, the cytoplasm was profoundly altered - chiefly the ribosomal apparatus, which, from a polyribosomal complex located peripherally in the cell, adjacent to the cytoplasmic membrane in the initial forms, has disintegrated into ribosomal units parts of which have often penetrated deeply in the nucleotide mass. Individual ribosomes remained connected with each other through DNA filaments, but there were equally cases in which links of such types were not present. The structure of the cytoplasmic membrane invariably showed three layers. The L forms obtained from R variants occasionally showed the presence of microtubules similar to those established with other microorganisms. Such structures were missing in the L forms obtained from S variants.
Download full-text PDF |
Source |
---|
Plant Biol (Stuttg)
January 2025
Department of Chemical Ecology, Bielefeld University, Bielefeld, Germany.
Plant individuals within a species can differ markedly in their leaf chemical composition, forming so-called chemotypes. Little is known about whether such differences impact the microbial communities associated with leaves and how different environmental conditions may shape these relationships. We used Tanacetum vulgare as a model plant to study the impacts of maternal effects, leaf terpenoid chemotype, and the environment on the leaf bacterial community by growing plant clones in the field and a greenhouse.
View Article and Find Full Text PDFNeural Regen Res
January 2025
Genome Dynamics and Function, Centro de Biología Molecular Severo Ochoa, CSIC-UAM, Madrid, Spain.
GEMIN5 is a predominantly cytoplasmic multifunctional protein, known to be involved in recognizing snRNAs through its WD40 repeats domain placed at the N-terminus. A dimerization domain in the middle region acts as a hub for protein-protein interaction, while a non-canonical RNA-binding site is placed towards the C-terminus. The singular organization of structural domains present in GEMIN5 enables this protein to perform multiple functions through its ability to interact with distinct partners, both RNAs and proteins.
View Article and Find Full Text PDFHGG Adv
January 2025
Insitro, South San Francisco, CA, USA.
Genome-wide association studies (GWAS) are often performed on ratios composed of a numerator trait divided by a denominator trait. Examples include body mass index (BMI) and the waist-to-hip ratio, among many others. Explicitly or implicitly, the goal of forming the ratio is typically to adjust for an association between the numerator and denominator.
View Article and Find Full Text PDFTrends Biotechnol
January 2025
College of Biological Sciences, China Agricultural University, Beijing 100193, China. Electronic address:
Engineering nitrogen fixation in cereals could reduce usage of chemical nitrogen fertilizers. Here, a nitrogenase biosynthesis pathway comprising 13 genes (nifB nifH nifD nifK nifE nifN nifX hesA nifV nifS nifU groES groEL) was introduced into rice by transforming multigene vectors and subsequently by sexual crossing between transgenic rice plants. Genome sequencing analysis revealed that 13 nif genes in F hybrid rice lines L12-13 and L8-17 were inserted at two loci on rice chromosome 1.
View Article and Find Full Text PDFAnn Endocrinol (Paris)
January 2025
Univ. Lille, Inserm, CHU Lille, U1286 - Infinite, F-59045 Lille Cedex, Department of Biochemistry and Molecular Biology, Lille University Hospital, Lille, France. Electronic address:
Around 10% of cases of primary hyperparathyroidism are thought to be genetic in origin, some of which are part of a syndromic form such as multiple endocrine neoplasia types 1, 2A or 4 or hyperparathyroidism-jaw tumor syndrome, while the remainder are cases of isolated familial primary hyperparathyroidism. Recognition of these genetic forms is important to ensure appropriate management according to the gene and type of variant involved, but screening for a genetic cause is not justified in all patients presenting primary hyperparathyroidism. The indications for genetic analysis have made it possible to propose a decision tree that takes into account whether the presentation is familial or sporadic, syndromic or isolated, patient age, and histopathological type of parathyroid lesion.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!