Actin patch assembly proteins Las17p and Sla1p restrict cell wall growth to daughter cells and interact withcis-Golgi protein Kre6p

Yeast ◽  
2002 ◽  
Vol 19 (13) ◽  
pp. 1097-1112 ◽  
Author(s):  
Huijuan Li ◽  
Nicolas Pagé ◽  
Howard Bussey
Keyword(s):  
Cell Wall ◽  
Cell Wall Growth ◽  
Daughter Cells ◽  
Wall Growth ◽  
Golgi Protein ◽  
Actin Patch ◽  
Assembly Proteins

CELL WALL REPLICATION: I. CELL WALL GROWTH OF BACILLUS CEREUS AND BACILLUS MEGATERIUM

1964 ◽  
Vol 10 (1) ◽  
pp. 43-48 ◽  
Author(s):  
K. L. Chung ◽  
R. Z. Hawirko ◽  
P. K. Isaac
Keyword(s):  
Cell Wall ◽  
Bacillus Cereus ◽  
Bacillus Megaterium ◽  
Central Area ◽  
Cell Length ◽  
Cell Wall Growth ◽  
Daughter Cells ◽  
Wall Growth

Cell wall replication of Bacillus cereus and Bacillus megaterium was studied by differential labelling with fluorescent and non-fluorescent antibody.Growth of new cell wall in B. cereus was initiated near the poles. In the old wall, additional new wall segments gradually developed to form an alternating pattern of new and old wall segments. Further growth elongated the new wall and pushed the old segments apart. Separation of daughter cells appeared to involve splitting of the transverse septa laid down at or near the old wall segments.Growth of new cell wall of B. megaterium was initiated either at one of the poles or at the central area of the cell. Multiple segments of new and old wall appeared along the cell length. Further elongation was followed by formation of transverse septa and separation of daughter cells incorporating either old or new wall segments.Our evidence clearly shows that growth and elongation of the two bacilli do not occur by diffuse intercalation of new cell wall into the old.

scholarly journals Probing bacterial cell wall growth by tracing wall-anchored protein complexes

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Yi-Jen Sun ◽  
Fan Bai ◽  
An-Chi Luo ◽  
Xiang-Yu Zhuang ◽  
Tsai-Shun Lin ◽  
...  
Keyword(s):  
Cell Wall ◽  
Cell Shape ◽  
Bernoulli Shift ◽  
Protein Complexes ◽  
Axial Direction ◽  
Cell Wall Growth ◽  
Flagellar Motors ◽  
Shift Map ◽  
Dynamic Assembly ◽  
Wall Growth

AbstractThe dynamic assembly of the cell wall is key to the maintenance of cell shape during bacterial growth. Here, we present a method for the analysis of Escherichia coli cell wall growth at high spatial and temporal resolution, which is achieved by tracing the movement of fluorescently labeled cell wall-anchored flagellar motors. Using this method, we clearly identify the active and inert zones of cell wall growth during bacterial elongation. Within the active zone, the insertion of newly synthesized peptidoglycan occurs homogeneously in the axial direction without twisting of the cell body. Based on the measured parameters, we formulate a Bernoulli shift map model to predict the partitioning of cell wall-anchored proteins following cell division.

Localisation of the Schizosaccharomyces pombe rho1p GTPase and its involvement in the organisation of the actin cytoskeleton

1997 ◽  
Vol 110 (20) ◽  
pp. 2547-2555 ◽  
Author(s):  
M. Arellano ◽  
A. Duran ◽  
P. Perez
Keyword(s):  
Cell Wall ◽  
Actin Cytoskeleton ◽  
Schizosaccharomyces Pombe ◽  
Antifungal Drugs ◽  
Dominant Negative ◽  
Cortical Actin ◽  
Glucan Synthase ◽  
Cell Wall Growth ◽  
Wall Growth ◽  
Mutant Cells

The Schizosaccharomyces pombe rho1p GTPase directly activates the (1–3) beta-D-glucan synthase and participates in the regulation of cell wall growth and morphogenesis in this fission yeast. Indirect immunofluorescence experiments using rho1p tagged with hemagglutinin have revealed that rho1p was located at the growing tips during interphase and at the septum prior to cytokinesis, localising to the same areas as actin patches. In S. pombe cdc10-129 mutant cells, arrested in G1, HA-rho1p accumulates at one tip whereas in cdc25-22 mutants, arrested in G2, HA-rho1p accumulates at both tips. In tea1-1 and tea2-1 cdc11-119 mutant cells, HA-rho1p is localised to the new growing tips. Overexpression of different rho1 mutant alleles caused different effects on cortical actin patch distribution, (1–3) beta-D-glucan synthase activation, and sensitivity to cell wall specific antifungal drugs. These results indicate that multiple cellular components are activated by rho1p. Overexpression of the dominant negative rho1T20N allele was lethal as was the rho1+ deletion. Moreover, when rho1+ expression was repressed in actively growing S. pombe, cells died in about 10 to 12 hours. Under these conditions, normal cell morphology was maintained but the level of (1–3) beta-D-glucan synthase activity decreased and the actin patches disappeared. Most cells lysed after cytokinesis during the process of separation, and lysis was not prevented by an osmotic stabiliser. We conclude that rho1p localisation is restricted to growth areas and regulated during the cell cycle and that rho1p is involved in cell wall growth and actin cytoskeleton organisation in S. pombe.

scholarly journals A geometrical model of Chara rhizoid growth

2014 ◽  
Vol 60 (1-2) ◽  
pp. 87-92
Author(s):  
Bogdan Ogrodnik
Keyword(s):  
Cell Wall ◽  
Growth Velocity ◽  
Geometrical Model ◽  
Cell Wall Growth ◽  
Chara Rhizoid ◽  
Wall Growth ◽  
Constant Deformation

The applicability of the Kirchoff-Love Hypothesis to the growth of the <i>Chara</i> rhizoid, approached as the constant deformation of the shell, was investigated. It is shown that the observed distribution of cell wall growth velocity may be, under certain assumptions, the result of the changing curvature of the growing surface.

scholarly journals The Mode of Cell Wall Growth in Selected Archaea Is Similar to the General Mode of Cell Wall Growth in Bacteria as Revealed by Fluorescent Dye Analysis

2010 ◽  
Vol 77 (5) ◽  
pp. 1556-1562 ◽  
Author(s):  
Reinhard Wirth ◽  
Annett Bellack ◽  
Markus Bertl ◽  
Yvonne Bilek ◽  
Thomas Heimerl ◽  
...  
Keyword(s):  
Cell Wall ◽  
Fluorescent Dyes ◽  
Pyrococcus Furiosus ◽  
Wall Material ◽  
Cell Wall Material ◽  
Cell Wall Growth ◽  
Archaeal Species ◽  
Dye Analysis ◽  
Wall Growth ◽  
Methanopyrus Kandleri

ABSTRACTThe surfaces of 8 bacterial and 23 archaeal species, including many hyperthermophilicArchaea, could be stained using succinimidyl esters of fluorescent dyes. This allowed us for the first time to analyze the mode of cell wall growth inArchaeaby subculturing stained cells. The data obtained show that incorporation of new cell wall material inArchaeafollows the pattern observed forBacteria: in the coccoid speciesPyrococcus furiosusincorporation was in the region of septum formation while for the rod-shaped speciesMethanopyrus kandleriandMethanothermus sociabilis, a diffuse incorporation of cell wall material over the cell length was observed. Cell surface appendages like fimbriae/pili, fibers, or flagella were detectable by fluorescence staining only in a very few cases although their presence was proven by electron microscopy. Our data in addition prove that Alexa Fluor dyes can be used forin situanalyses at temperatures up to 100°C.

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