Dimension control in Micrococcus flavus

1972 ◽  
Vol 18 (11) ◽  
pp. 1721-1725 ◽  
Author(s):  
R. J. L. Paulton
Keyword(s):  
Growth Rate ◽  
Cell Separation ◽  
Generation Time ◽  
Gram Positive Bacteria ◽  
Septum Formation ◽  
Division Site ◽  
Dimension Control ◽  
Cell Age ◽  
Cell Dimensions ◽  
Constant Cell

The effect of nutrition on growth rate, cell size, and cell arrangement in Micrococcus flavus is described in relation to earlier studies of other bacteria. Progressive improvements in nutrition reduced the generation time from 15 to 1.7 h (at 25 °C), but septum formation occurred at about the same cell age in all growth cycles. In Gram-negative bacteria, the division site is also formed at a constant cell age, just before cell separation so that cells occur singly. In M. flavus, however, the time between septum formation and the related cell separation exceeded one generation time so that cells were either in pairs or tetrads. This arrangement of cells in groups is more typical of Gram-positive bacteria. The change in cell dimensions from hemispheres to spheres was also found to occur in M. flavus at a constant cell age, just before septum formation. With reference to three taxonomically unrelated bacteria, the arrangement of cells in groups is shown to result from the interrelation between growth rate and the timing of septum formation within the cell cycle.

Dimension control in bacteria

1974 ◽  
Vol 20 (2) ◽  
pp. 231-236 ◽  
Author(s):  
Edward G. Sedgwick ◽  
Richard J. L. Paulton
Keyword(s):  
Growth Rate ◽  
Bacillus Subtilis ◽  
Cell Size ◽  
Growth Rates ◽  
Individual Cell ◽  
Cell Number ◽  
Cell Arrangement ◽  
Dimension Control ◽  
Constant Cell ◽  
The Individual

The effect of nutrition on the relation between growth rate and cell arrangement, cell size, and macro-molecular composition in Bacillus subtilis is described in comparison to earlier observations with other bacteria. Improvements in nutrition resulted in faster growth rates but, although the mass and size of the replicating unit (i.e. cell number/chain) also increased, there was no change in the mass or size of the individual cell. This constant cell size and variable cell arrangement in B. subtilis is in contrast to other bacteria and requires new proposals for the control of cell size and arrangement in different bacteria.

scholarly journals The Consequences of Budding versus Binary Fission on Adaptation and Aging in Primitive Multicellularity

Genes ◽  
2021 ◽  
Vol 12 (5) ◽  
pp. 661
Author(s):  
Hanna Isaksson ◽  
Peter L. Conlin ◽  
Ben Kerr ◽  
William C. Ratcliff ◽  
Eric Libby
Keyword(s):  
Cell Cycle ◽  
Growth Rate ◽  
Cellular Senescence ◽  
Carrying Capacity ◽  
The Other ◽  
Binary Fission ◽  
Fundamental Aspect ◽  
Accumulated Damage ◽  
Cell Age ◽  
Multicellular Organisms

Early multicellular organisms must gain adaptations to outcompete their unicellular ancestors, as well as other multicellular lineages. The tempo and mode of multicellular adaptation is influenced by many factors including the traits of individual cells. We consider how a fundamental aspect of cells, whether they reproduce via binary fission or budding, can affect the rate of adaptation in primitive multicellularity. We use mathematical models to study the spread of beneficial, growth rate mutations in unicellular populations and populations of multicellular filaments reproducing via binary fission or budding. Comparing populations once they reach carrying capacity, we find that the spread of mutations in multicellular budding populations is qualitatively distinct from the other populations and in general slower. Since budding and binary fission distribute age-accumulated damage differently, we consider the effects of cellular senescence. When growth rate decreases with cell age, we find that beneficial mutations can spread significantly faster in a multicellular budding population than its corresponding unicellular population or a population reproducing via binary fission. Our results demonstrate that basic aspects of the cell cycle can give rise to different rates of adaptation in multicellular organisms.

scholarly journals Roles of the novel coiled-coil protein Rng10 in septum formation during fission yeast cytokinesis

2016 ◽  
Vol 27 (16) ◽  
pp. 2528-2541 ◽  
Author(s):  
Yajun Liu ◽  
I-Ju Lee ◽  
Mingzhai Sun ◽  
Casey A. Lower ◽  
Kurt W. Runge ◽  
...  
Keyword(s):  
Fission Yeast ◽  
Rho Gtpases ◽  
Cellular Localization ◽  
Affinity Purification ◽  
Coiled Coil ◽  
The Novel ◽  
Septum Formation ◽  
Division Site ◽  
And Function

Rho GAPs are important regulators of Rho GTPases, which are involved in various steps of cytokinesis and other processes. However, regulation of Rho-GAP cellular localization and function is not fully understood. Here we report the characterization of a novel coiled-coil protein Rng10 and its relationship with the Rho-GAP Rga7 in fission yeast. Both rng10Δ and rga7Δ result in defective septum and cell lysis during cytokinesis. Rng10 and Rga7 colocalize on the plasma membrane at the cell tips during interphase and at the division site during cell division. Rng10 physically interacts with Rga7 in affinity purification and coimmunoprecipitation. Of interest, Rga7 localization is nearly abolished without Rng10. Moreover, Rng10 and Rga7 work together to regulate the accumulation and dynamics of glucan synthases for successful septum formation in cytokinesis. Our results show that cellular localization and function of the Rho-GAP Rga7 are regulated by a novel protein, Rng10, during cytokinesis in fission yeast.

Cibacron blue 3G-A inhibits cell separation of gram-positive bacteria

1991 ◽  
Vol 155 (2) ◽  
pp. 199-201 ◽  
Author(s):  
Motoyuki Sugai ◽  
Tomoko Akiyama ◽  
Hitoshi Komatsuzawa ◽  
Yoichiro Miyake ◽  
Hidekazu Suginaka
Keyword(s):  
Cell Separation ◽  
Gram Positive ◽  
Cibacron Blue ◽  
Gram Positive Bacteria

Validation and Analysis of Modeled Predictions of Growth of Bacillus cereus Spores in Boiled Rice

2000 ◽  
Vol 63 (2) ◽  
pp. 268-272 ◽  
Author(s):  
DANA M. McELROY ◽  
LEE-ANN JAYKUS ◽  
PEGGY M. FOEGEDING
Keyword(s):  
Growth Rate ◽  
Bacillus Cereus ◽  
Exponential Growth ◽  
Generation Time ◽  
Time Lag ◽  
Lag Phase ◽  
Exponential Growth Rate ◽  
Phase Duration ◽  
Margin Of Safety ◽  
Fail Safe

The growth of psychrotrophic Bacillus cereus 404 from spores in boiled rice was examined experimentally at 15, 20, and 30°C. Using the Gompertz function, observed growth was modeled, and these kinetic values were compared with kinetic values for the growth of mesophilic vegetative cells as predicted by the U.S. Department of Agriculture's Pathogen Modeling Program, version 5.1. An analysis of variance indicated no statistically significant difference between observed and predicted values. A graphical comparison of kinetic values demonstrated that modeled predictions were “fail safe” for generation time and exponential growth rate at all temperatures. The model also was fail safe for lag-phase duration at 20 and 30°C but not at l5°C. Bias factors of 0.55, 0.82, and 1.82 for generation time, lag-phase duration, and exponential growth rate, respectively, indicated that the model generally was fail safe and hence provided a margin of safety in its growth predictions. Accuracy factors of 1.82, 1.60, and 1.82 for generation time, lag-phase duration, and exponential growth rate, respectively, quantitatively demonstrated the degree of difference between predicted and observed values. Although the Pathogen Modeling Program produced reasonably accurate predictions of the growth of psychrotrophic B. cereus from spores in boiled rice, the margin of safety provided by the model may be more conservative than desired for some applications. It is recommended that if microbial growth modeling is to be applied to any food safety or processing situation, it is best to validate the model before use. Once experimental data are gathered, graphical and quantitative methods of analysis can be useful tools for evaluating specific trends in model prediction and identifying important deviations between predicted and observed data.

Regulation of the start of DNA replication in Schizosaccharomyces pombe

1999 ◽  
Vol 112 (6) ◽  
pp. 939-946 ◽  
Author(s):  
C.R. Carlson ◽  
B. Grallert ◽  
T. Stokke ◽  
E. Boye
Keyword(s):  
Cell Cycle ◽  
Flow Cytometry ◽  
Growth Rate ◽  
Schizosaccharomyces Pombe ◽  
Growth Rates ◽  
Cell Separation ◽  
Cell Mass ◽  
Nitrogen Sources ◽  
S Phase ◽  
G1 Phase

Cells of Schizosaccharomyces pombe were grown in minimal medium with different nitrogen sources under steady-state conditions, with doubling times ranging from 2.5 to 14 hours. Flow cytometry and fluorescence microscopy confirmed earlier findings that at rapid growth rates, the G1 phase was short and cell separation occurred at the end of S phase. For some nitrogen sources, the growth rate was greatly decreased, the G1 phase occupied 30–50% of the cell cycle, and cell separation occurred in early G1. In contrast, other nitrogen sources supported low growth rates without any significant increase in G1 duration. The method described allows manipulation of the length of G1 and the relative cell cycle position of S phase in wild-type cells. Cell mass was measured by flow cytometry as scattered light and as protein-associated fluorescence. The extensions of G1 were not related to cell mass at entry into S phase. Our data do not support the hypothesis that the cells must reach a certain fixed, critical mass before entry into S. We suggest that cell mass at the G1/S transition point is variable and determined by a set of molecular parameters. In the present experiments, these parameters were influenced by the different nitrogen sources in a way that was independent of the actual growth rate.

scholarly journals The Tol-Pal system is required for peptidoglycan-cleaving enzymes to complete bacterial cell division

2020 ◽  
Vol 117 (12) ◽  
pp. 6777-6783 ◽  
Author(s):  
Anastasiya A. Yakhnina ◽  
Thomas G. Bernhardt
Keyword(s):  
Cell Separation ◽  
Glycosyl Hydrolase ◽  
Gram Negative Bacteria ◽  
Bacterial Cell Division ◽  
General Role ◽  
E Coli ◽  
Division Site ◽  
Genetic Suppressors ◽  
Bacteria Inactivation ◽  
Mutant Cells

Tol-Pal is a multiprotein system present in the envelope of Gram-negative bacteria. Inactivation of this widely conserved machinery compromises the outer membrane (OM) layer of these organisms, resulting in hypersensitivity to many antibiotics. Mutants in thetol-pallocus fail to complete division and form cell chains. This phenotype along with the localization of Tol-Pal components to the cytokinetic ring inEscherichia colihas led to the proposal that the primary function of the system is to promote OM constriction during division. Accordingly, a poorly constricted OM is believed to link the cell chains formed upon Tol-Pal inactivation. However, we show here that cell chains ofE. coli tol-palmutants are connected by an incompletely processed peptidoglycan (PG) layer. Genetic suppressors of this defect were isolated and found to overproduce OM lipoproteins capable of cleaving the glycan strands of PG. Among the factors promoting cell separation in mutant cells was a protein of previously unknown function (YddW), which we have identified as a divisome-localized glycosyl hydrolase that cleaves peptide-free PG glycans. Overall, our results indicate that the cell chaining defect of Tol-Pal mutants cannot simply be interpreted as a defect in OM constriction. Rather, the complex also appears to be required for the activity of several OM-localized enzymes with cell wall remodeling activity. Thus, the Tol-Pal system may play a more general role in coordinating OM invagination with PG remodeling at the division site than previously appreciated.

scholarly journals Scw1p Antagonizes the Septation Initiation Network To Regulate Septum Formation and Cell Separation in the Fission Yeast Schizosaccharomyces pombe

2003 ◽  
Vol 2 (3) ◽  
pp. 510-520 ◽  
Author(s):  
Quan-Wen Jin ◽  
Dannel McCollum
Keyword(s):  
Schizosaccharomyces Pombe ◽  
Fission Yeast ◽  
Cell Separation ◽  
Deletion Mutant ◽  
Temperature Sensitive ◽  
Growth Defects ◽  
Septum Formation ◽  
Primary Septum ◽  
Septation Initiation Network ◽  
Ring Constriction

ABSTRACT Cytokinesis in the fission yeast Schizosaccharomyces pombe is regulated by a signaling pathway termed the septation initiation network (SIN). The SIN is essential for initiation of actomyosin ring constriction and septum formation. In a screen to search for mutations that can rescue the sid2-250 SIN mutant, we obtained scw1-18. Both the scw1-18 mutant and the scw1 deletion mutant (scw1Δ mutant), have defects in cell separation. Both the scw1-18 and scw1Δ mutations rescue the growth defects of not just the sid2-250 mutant but also the other temperature-sensitive SIN mutants. Other cytokinesis mutants, such as those defective for actomyosin ring formation, are not rescued by scw1Δ. scw1Δ does not seem to rescue the SIN by restoring SIN signaling defects. However, scw1Δ may function downstream of the SIN to promote septum formation, since scw1Δ can rescue the septum formation defects of the cps1-191β-1,3-glucan synthase mutant, which is required for synthesis of the primary septum.

scholarly journals Lipid droplets maintain lipid homeostasis during anaphase for efficient cell separation in budding yeast

2016 ◽  
Vol 27 (15) ◽  
pp. 2368-2380 ◽  
Author(s):  
Po-Lin Yang ◽  
Tzu-Han Hsu ◽  
Chao-Wen Wang ◽  
Rey-Huei Chen
Keyword(s):  
Cell Separation ◽  
Neutral Lipids ◽  
Budding Yeast ◽  
Acid Synthesis ◽  
Mitotic Exit ◽  
Lipid Homeostasis ◽  
Physiological Conditions ◽  
Division Site ◽  
Quadruple Mutant ◽  
Membrane Bound

The neutral lipids steryl ester and triacylglycerol (TAG) are stored in the membrane-bound organelle lipid droplet (LD) in essentially all eukaryotic cells. It is unclear what physiological conditions require the mobilization or storage of these lipids. Here, we study the budding yeast mutant are1Δ are2Δ dga1Δ lro1Δ, which cannot synthesize the neutral lipids and therefore lacks LDs. This quadruple mutant is delayed at cell separation upon release from mitotic arrest. The cells have abnormal septa, unstable septin assembly during cytokinesis, and prolonged exocytosis at the division site at the end of cytokinesis. Lipidomic analysis shows a marked increase of diacylglycerol (DAG) and phosphatidic acid, the precursors for TAG, in the mutant during mitotic exit. The cytokinesis and separation defects are rescued by adding phospholipid precursors or inhibiting fatty acid synthesis, which both reduce DAG levels. Our results suggest that converting excess lipids to neutral lipids for storage during mitotic exit is important for proper execution of cytokinesis and efficient cell separation.

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