Aerosol survival of Serratia marcescens as a function of oxygen concentration, relative humidity, and time

1974 ◽  
Vol 20 (11) ◽  
pp. 1529-1534 ◽  
Author(s):  
C. S. Cox ◽  
S. J. Gagen ◽  
Jean Baxter
Keyword(s):  
Cell Wall ◽  
Cell Division ◽  
Relative Humidity ◽  
Serratia Marcescens ◽  
Oxygen Concentration ◽  
Freeze Drying ◽  
Cytoplasmic Membrane ◽  
Cell Wall Synthesis ◽  
Freeze Dried ◽  
Kinetics Of

Previously the kinetics of loss of viability of freeze-dried Serratia marcescens 8UK were determined by Cox and Heckly as a function of oxygen concentration and time. Results are presented here when dehydration is brought about by aerosolization into atmospheres of low relative humidity (RH) rather than by freeze-drying. As for freeze-dried S. marcescens, oxygen was toxic and viable decay followed the same kinetics with respect to oxygen concentration and time. The influence of RH upon viable decay (which was not studied in the previous report) was that above 65% RH oxygen was not toxic but was progressively more toxic as the humidity was further reduced. Kinetic analyses of the results indicate that the site for the toxic action of oxygen lies in the interspace between the cytoplasmic membrane and the cell wall. Such a finding is consistent with other data which suggest that cell division and (or) cell wall synthesis in bacteria are inhibited by oxygen.

scholarly journals Treadmilling by FtsZ filaments drives peptidoglycan synthesis and bacterial cell division

2016 ◽  
Author(s):  
Alexandre W. Bisson Filho ◽  
Yen-Pang Hsu ◽  
Georgia R. Squyres ◽  
Erkin Kuru ◽  
Fabai Wu ◽  
...  
Keyword(s):  
Cell Wall ◽  
Cell Division ◽  
Division Ring ◽  
Bacterial Cell ◽  
Cytoplasmic Membrane ◽  
Bacterial Cell Division ◽  
Cell Wall Synthesis ◽  
Division Plane ◽  
Peptidoglycan Synthesis

AbstractHow bacteria produce a septum to divide in two is not well understood. This process is mediated by periplasmic cell-wall producing enzymes that are positioned by filaments of the cytoplasmic membrane-associated actin FtsA and the tubulin FtsZ (FtsAZ). To understand how these components act in concert to divide cells, we visualized their movements relative to the dynamics of cell wall synthesis during cytokinesis. We find that the division septum is built at discrete sites that move around the division plane. Furthermore, FtsAZ filaments treadmill in circumferential paths around the division ring, pulling along the associated cell-wall-synthesizing enzymes. We show that the rate of FtsZ treadmilling controls both the rate of cell wall synthesis and cell division. The coupling of both the position and activity of the cell wall synthases to FtsAZ treadmilling guides the progressive insertion of new cell wall, synthesizing increasingly small concentric rings to divide the cell.One-sentence summaryBacterial cytokinesis is controlled by circumferential treadmilling of FtsAZ filaments that drives the insertion of new cell wall.

ABNORMAL GROWTH INDUCED BY PENICILLIN IN A STRAIN OF ALCALIGENES FECALIS

1958 ◽  
Vol 4 (2) ◽  
pp. 165-177 ◽  
Author(s):  
K. G. Lark
Keyword(s):  
Cell Wall ◽  
Cell Division ◽  
Exponential Growth ◽  
Division Rate ◽  
Abnormal Growth ◽  
Globular Form ◽  
Kinetics Of

The effect of penicillin on strain LB of Alcaligenes fccalis has been studied. In tryptone, 50 units/ml. of penicillin transforms the bacillary form of this organism into a protoplast-like structure (globular form) which is capable of exponential growth and division. The division rate of this globular form is about one-half that of the bacillary form. Removal of penicillin results in the reversion of the globular to the bacillary form. Multiplication of the globular form has been found to depend on the presence of some principle present in tryptone not required for bacillary growth in the absence of penicillin. The kinetics of the transformation and reversion process have been studied, leading to the hypothesis that penicillin affects some component: within the cell, this component being concerned with cell division and the elaboration of the cell wall.

scholarly journals Morphology and Release Kinetics of Protein-Loaded Porous Poly(L-Lactic Acid) Spheres Prepared by Freeze-Drying Technique

2011 ◽  
Vol 2011 ◽  
pp. 1-8 ◽  
Author(s):  
Takashi Sasaki ◽  
Kazuki Tanaka ◽  
Daisuke Morino ◽  
Kensuke Sakurai
Keyword(s):  
Lactic Acid ◽  
Freeze Drying ◽  
Release Kinetics ◽  
Particle Surface ◽  
Spherical Particles ◽  
Freeze Dried ◽  
Model Drug ◽  
Drug Compound ◽  
Kinetics Of ◽  
Step Mechanism

Freeze-drying a biodegradable polymer, poly(L-lactic acid) (PLLA), from 1,4-dioxane solutions provided very porous spherical particles of ca. 3 mm in radius with specific surface area of 8–13 m2 g−1. The surface of the particle was found to be less porous compared with its interior. To apply the freeze-dried PLLA (FDPLLA) to drug delivery system, its morphology and drug releasing kinetics were investigated, bovine serum albumin (BSA) being used as a model drug compound. Immersion of FDPLLA into a BSA aqueous solution gave BSA-loaded FDPLLA, where mass fraction of the adsorbed BSA reached up to 79%. Time-dependent release profile of BSA in water suggested a two-step mechanism: (1) very rapid release of BSA deposited on and near the particle surface, which results in an initial burst, and (2) leaching of BSA from the interior of the particle by the diffusion process. It was suggested that the latter process is largely governed by the surface porosity. The porosity of both the interior and surface was found to decrease remarkably as the concentration of the original PLLA/1,4-dioxane solution increases, C0. Thus, C0 is a key parameter that controls the loading and releasing of BSA.

scholarly journals Bacteriophage SP01 Gene Product 56 Inhibits Bacillus subtilis Cell Division by Interacting with FtsL and Disrupting Pbp2B and FtsW Recruitment

2020 ◽  
Vol 203 (2) ◽  
pp. e00463-20
Author(s):  
Amit Bhambhani ◽  
Isabella Iadicicco ◽  
Jules Lee ◽  
Syed Ahmed ◽  
Max Belfatto ◽  
...  
Keyword(s):  
Cell Wall ◽  
Bacillus Subtilis ◽  
Cell Division ◽  
Gene Product ◽  
Fluorescent Protein ◽  
Lytic Bacteriophage ◽  
Cell Wall Synthesis ◽  
Content Type ◽  
Ftsz Ring ◽  
Green Fluorescent

ABSTRACTPrevious work identified gene product 56 (gp56), encoded by the lytic bacteriophage SP01, as being responsible for inhibition of Bacillus subtilis cell division during its infection. Assembly of the essential tubulin-like protein FtsZ into a ring-shaped structure at the nascent site of cytokinesis determines the timing and position of division in most bacteria. This FtsZ ring serves as a scaffold for recruitment of other proteins into a mature division-competent structure permitting membrane constriction and septal cell wall synthesis. Here, we show that expression of the predicted 9.3-kDa gp56 of SP01 inhibits later stages of B. subtilis cell division without altering FtsZ ring assembly. Green fluorescent protein-tagged gp56 localizes to the membrane at the site of division. While its localization does not interfere with recruitment of early division proteins, gp56 interferes with the recruitment of late division proteins, including Pbp2b and FtsW. Imaging of cells with specific division components deleted or depleted and two-hybrid analyses suggest that gp56 localization and activity depend on its interaction with FtsL. Together, these data support a model in which gp56 interacts with a central part of the division machinery to disrupt late recruitment of the division proteins involved in septal cell wall synthesis.IMPORTANCE Studies over the past decades have identified bacteriophage-encoded factors that interfere with host cell shape or cytokinesis during viral infection. The phage factors causing cell filamentation that have been investigated to date all act by targeting FtsZ, the conserved prokaryotic tubulin homolog that composes the cytokinetic ring in most bacteria and some groups of archaea. However, the mechanisms of several phage factors that inhibit cytokinesis, including gp56 of bacteriophage SP01 of Bacillus subtilis, remain unexplored. Here, we show that, unlike other published examples of phage inhibition of cytokinesis, gp56 blocks B. subtilis cell division without targeting FtsZ. Rather, it utilizes the assembled FtsZ cytokinetic ring to localize to the division machinery and to block recruitment of proteins needed for septal cell wall synthesis.

scholarly journals The Antituberculosis Drug Ethambutol Selectively Blocks Apical Growth in CMN Group Bacteria

mBio ◽  
2017 ◽  
Vol 8 (1) ◽  
Author(s):  
Karin Schubert ◽  
Boris Sieger ◽  
Fabian Meyer ◽  
Giacomo Giacomelli ◽  
Kati Böhm ◽  
...  
Keyword(s):  
Cell Wall ◽  
Cell Division ◽  
Cell Growth ◽  
Antibiotic Treatment ◽  
Bacterial Infections ◽  
Apical Cell ◽  
Combined Treatment ◽  
Mycolic Acid ◽  
Cell Wall Synthesis ◽  
Beta Lactam

ABSTRACT Members of the genus Mycobacterium are the most prevalent cause of infectious diseases. Mycobacteria have a complex cell envelope containing a peptidoglycan layer and an additional arabinogalactan polymer to which a mycolic acid bilayer is linked; this complex, multilayered cell wall composition (mAGP) is conserved among all CMN group bacteria. The arabinogalactan and mycolic acid synthesis pathways constitute effective drug targets for tuberculosis treatment. Ethambutol (EMB), a classical antituberculosis drug, inhibits the synthesis of the arabinose polymer. Although EMB acts bacteriostatically, its underlying molecular mechanism remains unclear. Here, we used Corynebacterium glutamicum and Mycobacterium phlei as model organisms to study the effects of EMB at the single-cell level. Our results demonstrate that EMB specifically blocks apical cell wall synthesis, but not cell division, explaining the bacteriostatic effect of EMB. Furthermore, the data suggest that members of the family Corynebacterineae have two dedicated machineries for cell elongation (elongasome) and cytokinesis (divisome). IMPORTANCE Antibiotic treatment of bacterial pathogens has contributed enormously to the increase in human health. Despite the apparent importance of antibiotic treatment of bacterial infections, surprisingly little is known about the molecular functions of antibiotic actions in the bacterial cell. Here, we analyzed the molecular effects of ethambutol, a first-line antibiotic against infections caused by members of the genus Mycobacterium. We find that this drug selectively blocks apical cell growth but still allows for effective cytokinesis. As a consequence, cells survive ethambutol treatment and adopt a pneumococcal cell growth mode with cell wall synthesis only at the site of cell division. However, combined treatment of ethambutol and beta-lactam antibiotics acts synergistically and effectively stops cell proliferation. IMPORTANCE Antibiotic treatment of bacterial pathogens has contributed enormously to the increase in human health. Despite the apparent importance of antibiotic treatment of bacterial infections, surprisingly little is known about the molecular functions of antibiotic actions in the bacterial cell. Here, we analyzed the molecular effects of ethambutol, a first-line antibiotic against infections caused by members of the genus Mycobacterium. We find that this drug selectively blocks apical cell growth but still allows for effective cytokinesis. As a consequence, cells survive ethambutol treatment and adopt a pneumococcal cell growth mode with cell wall synthesis only at the site of cell division. However, combined treatment of ethambutol and beta-lactam antibiotics acts synergistically and effectively stops cell proliferation.

Bactericidal action of peptide antibiotic AS-48 against Escherichia coli K-12

1989 ◽  
Vol 35 (2) ◽  
pp. 318-321 ◽  
Author(s):  
A. Gálvez ◽  
E. Valdivia ◽  
M. Martínez ◽  
M. Maqueda
Keyword(s):  
Escherichia Coli ◽  
Cell Wall ◽  
Cell Growth ◽  
Mode Of Action ◽  
Cytoplasmic Membrane ◽  
Peptide Antibiotic ◽  
Biosynthetic Pathways ◽  
Bactericidal Action ◽  
Cell Wall Synthesis ◽  
K 12

Peptide antibiotic AS-48 exerts a bactericidal mode of action on exponential cultures of Escherichia coli K-12 through a multi-hit kinetics interaction. AS-48 causes a parallel and gradual cessation of all biosynthetic pathways monitored (protein, RNA, DNA, and cell wall synthesis), the rate of incorporation of labeled precursors, the rate of O2 consumption, and cell growth. These effects have been attributed to alterations of cytoplasmic membrane functions.Key words: Escherichia coli, peptide antibiotic, bactericide.

Analysis of Freeze-Drying and Rehydration of Açai (Euterpe oleracea Martius)

2015 ◽  
Vol 365 ◽  
pp. 11-16
Author(s):  
R.J. Brandão ◽  
M.M. Prado ◽  
L.G. Marques
Keyword(s):  
Mass Transfer ◽  
Energy Demand ◽  
Freeze Drying ◽  
Moisture Diffusion ◽  
Euterpe Oleracea ◽  
Power Ultrasound ◽  
Ultrasound Waves ◽  
Freeze Dried ◽  
Peleg’S Equation ◽  
Kinetics Of

The freeze-drying rate is essentially low, since it is controlled by internal moisture diffusion. In addition, the application of vacuum and low temperature during the process presents a higher energy demand. Therefore, the search for new strategies to improve water mobility during freeze-drying constitutes a topic of relevant research. The aim of this work was to evaluate the use of power ultrasound to improve freeze-drying characteristics of açai, quantifying the influence of the applied power on both the drying and rehydration kinetics of the material. Açai (Euterpe oleracea Martius) samples were sonicated with two different frequency levels, 20 kHz and 40 kHz, and two sonication times, 3 min and 10 min. Page’s equation considering internal and external resistances to mass transfer provided a good fit of freeze-drying kinetics, while the Peleg’s equation was found to be suitable for describing the rehydration kinetics of freeze-dried açai. Pretreatment of açai with ultrasound waves was not effective. Ultrasound-induced structural disruption in the açai skin hindered the mass transfer during both freeze-drying and rehydration processes.

scholarly journals The heat-shock response of Listeria monocytogenes comprises genes involved in heat shock, cell division, cell wall synthesis, and the SOS response

Microbiology ◽  
2007 ◽  
Vol 153 (10) ◽  
pp. 3593-3607 ◽  
Author(s):  
Stijn van der Veen ◽  
Torsten Hain ◽  
Jeroen A. Wouters ◽  
Hamid Hossain ◽  
Willem M. de Vos ◽  
...  
Keyword(s):  
Cell Wall ◽  
Cell Division ◽  
Listeria Monocytogenes ◽  
Heat Shock ◽  
Heat Shock Response ◽  
Sos Response ◽  
Cell Wall Synthesis ◽  
Shock Cell ◽  
Shock Response ◽  
Division Cell

scholarly journals DivIVA Is Required for Polar Growth in the MreB-Lacking Rod-Shaped Actinomycete Corynebacterium glutamicum

2008 ◽  
Vol 190 (9) ◽  
pp. 3283-3292 ◽  
Author(s):  
Michal Letek ◽  
Efrén Ordóñez ◽  
José Vaquera ◽  
William Margolin ◽  
Klas Flärdh ◽  
...  
Keyword(s):  
Cell Wall ◽  
Bacillus Subtilis ◽  
Cell Division ◽  
Streptococcus Pneumoniae ◽  
Corynebacterium Glutamicum ◽  
Chromosome Segregation ◽  
Polar Growth ◽  
Cell Wall Synthesis ◽  
Peptidoglycan Synthesis ◽  
Polarized Cell Growth

ABSTRACT The actinomycete Corynebacterium glutamicum grows as rod-shaped cells by zonal peptidoglycan synthesis at the cell poles. In this bacterium, experimental depletion of the polar DivIVA protein (DivIVACg) resulted in the inhibition of polar growth; consequently, these cells exhibited a coccoid morphology. This result demonstrated that DivIVA is required for cell elongation and the acquisition of a rod shape. DivIVA from Streptomyces or Mycobacterium localized to the cell poles of DivIVACg-depleted C. glutamicum and restored polar peptidoglycan synthesis, in contrast to DivIVA proteins from Bacillus subtilis or Streptococcus pneumoniae, which localized at the septum of C. glutamicum. This confirmed that DivIVAs from actinomycetes are involved in polarized cell growth. DivIVACg localized at the septum after cell wall synthesis had started and the nucleoids had already segregated, suggesting that in C. glutamicum DivIVA is not involved in cell division or chromosome segregation.

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