Correlation between protonema morphogenesis and the development of the microtubule system in Funaria spore germination under normal conditions and at high auxin concentrations: an immunofluorescence study

1989 ◽  
Vol 67 (8) ◽  
pp. 2227-2234 ◽  
Author(s):  
N. Ljubešić ◽  
H. Quader ◽  
E. Schnepf
Keyword(s):  
Cell Division ◽  
Spore Germination ◽  
Germ Tube ◽  
Immunofluorescence Study ◽  
Cell Morphogenesis ◽  
Antimicrotubule Agents ◽  
High Concentrations ◽  
High Auxin

Ungerminated spores of Funaria do not contain distinct microtubules but show diffuse antitubulin antibody fluorescence. The microtubules arise when, 24–48 h after sowing, the spores are swollen and the first germ tube begins to protrude. Initially, diffuse fluorescence and microtubules are concentrated around the nucleus. Treatment with auxin at high concentrations (5 × 10−5 – 10−4 M) retards germination and cell division. Like antimicrotubule agents, such as colchicine and chloroisopropyl-N-phenylcarbamate, high auxin concentrations affect the formation of microtubules; either short, irregularly shaped microtubules and fluorescent spots arise, or there is no evidence of microtubules. The auxin effects on growth and microtubules can be reversed in less than 1 day. There is a correlation between the formation of the microtubule system and cell morphogenesis.

Aliphatic acids as spore germination inhibitors of wood-decay fungi in vitro

1985 ◽  
Vol 63 (2) ◽  
pp. 337-339 ◽  
Author(s):  
Elmer L. Schmidt
Keyword(s):  
Spore Germination ◽  
Germ Tube ◽  
White Rot Fungi ◽  
Wood Decay ◽  
White Rot ◽  
Malt Extract ◽  
Decay Fungi ◽  
Aliphatic Acids ◽  
Wood Decay Fungi

Influences of eight saturated aliphatic acids (C5–C10, C12, and C16) on basidiospores of four isolates of wood-decay fungi (Poria tenuis and Trametes hispida, white rot fungi, and two isolates of the brown rot fungus Gloeophyllum trabeum) were observed in vitro. Spore responses after 24 h on malt extract agar containing 10, 102 or 103 ppm of each acid included normal germination, delay of germ tube emergence, vacuolation and degeneration of spore cytoplasm, and prevention of germ tube development without spore destruction. Acids of chain length C5–C10 prevented spore germination and killed spores of all fungi at concentrations of 20–50 ppm in media, whereas other acids tested were less active. Spore germination assay of decay fungi may prove useful as a screening tool to compare potency of wood preservatives.

Factors influencing tartrate uptake by Penicillium charlesii

1968 ◽  
Vol 14 (5) ◽  
pp. 579-585 ◽  
Author(s):  
K. P. Klatt ◽  
J. E. Gander
Keyword(s):  
Spore Germination ◽  
Glucose Concentration ◽  
Factors Influencing ◽  
High Concentrations

The uptake of tartrate by P. charlesii has been studied for cultures that were either aerated by shaking or were kept stationary. Stationary cultures were permeable to tartrate when high concentrations of NH4+ (above 36 mM) and glucose (278 mM) were present. Manganous ion (10−5 M) was required for the uptake of tartrate by stationary cultures containing high concentrations of NH4+. Both stationary and shake cultures were able to remove tartrate from the medium when the glucose concentration was reduced below 278 mM; the process was then no longer dependent upon the presence of Mn2+. The influence of changes in the concentrations of glucose and NH4+ was not related to the biochemical events of spore germination.

scholarly journals CLASP localizes in two discrete patterns on cortical microtubules and is required for cell morphogenesis and cell division in Arabidopsis

2007 ◽  
Vol 120 (24) ◽  
pp. 4416-4425 ◽  
Author(s):  
V. Kirik ◽  
U. Herrmann ◽  
C. Parupalli ◽  
J. C. Sedbrook ◽  
D. W. Ehrhardt ◽  
...  
Keyword(s):  
Cell Division ◽  
Cortical Microtubules ◽  
Cell Morphogenesis

Microtubules and microfilaments in tip growth: evidence that microtubules impose polarity on protonemal growth in Physcomitrella patens

1988 ◽  
Vol 89 (4) ◽  
pp. 533-540 ◽  
Author(s):  
J. H. DOONAN ◽  
D. J. COVE ◽  
C. W. LLOYD
Keyword(s):  
Tip Growth ◽  
Physcomitrella Patens ◽  
Cytochalasin D ◽  
Immunofluorescence Study ◽  
Apical Dome ◽  
High Concentrations ◽  
Cytoskeletal Elements ◽  
Drug Studies ◽  
Tip Cells ◽  
Cytoskeletal Drugs

In this study we compare the contributions of Factin and microtubules to tip growth in filamentous cells of the moss Physcomitrella patens. In tip growth, expansion seems to be restricted to the hemispherical apical dome. Cytoskeletal elements have been suspected, from drug studies, to be involved in this but electron microscopy has generally not confirmed the presence of an apical cytoskeleton. However, in a previous immunofluorescence study we reported that microtubules could be seen to focus upon the apical dome in tip cells of the moss P. patens. In the present investigation F-actin has also been detected at the apices of these cells. Anti-cytoskeletal drugs were therefore used to differentiate between the roles of actin filaments and microtubules in tip growth. At high concentrations (30μM), the herbicide cremart de-polymerized microtubules and caused tip swelling. F-actin was still present under such conditions but its fragmentation by cytochalasin D suppressed this herbicide-induced swelling. On its own, cytochalasin D arrested tip growth without causing swollen tips. At lower concentrations, cremart disorganized microtubules rather than causing their complete depolymerization. Under these conditions, new but swollen growing points were initiated along the filament. The addition of taxol to cremart-treated filaments tended to reduce swelling and to re-polarize outgrowth. With particular combinations of these drugs, multiple lateral out-growths were initiated in the vicinity of the nucleus. It is concluded: (1) that F-actin is present at the tips of Physcomitrella caulonemal apical cells; (2) that unfragmented F-actin is necessary for outgrowth; (3) that even disorganized microtubules permit some degree of outgrowth but that an unperturbed distribution of axial microtubules, focussing upon an apex, is essential in order to impose tubular shape and directionality upon expansion.

scholarly journals Antifungal Efficacy of Plant Oils Containing Thymol and Carvacrol in Controlling Botrytis cinerea, the Causal Agent of Grape (Vitis vinifera) GrayMould

2018 ◽  
Vol 16 (02) ◽  
pp. 15-24
Author(s):  
Zaker M ◽  
Zaker L
Keyword(s):  
Essential Oils ◽  
Botrytis Cinerea ◽  
Spore Germination ◽  
Mycelial Growth ◽  
Germ Tube ◽  
Plant Diseases ◽  
Plant Oils ◽  
Horticultural Products ◽  
Antifungal Efficacy ◽  
Germ Tube Elongation

The efficacy of a large number of plant extracts and essential oils in controlling plant diseases has been proven worldwide. Botrytis cinerea has attacked a wide host range causing severe loss in the field and at storage. In this study the antifungal efficacy of essential oils of three medicinal plants namely wild marjoram (Zataria multifolia), wild savory (perennial) (Satureja mutica) and savory (annual) (Satureja hortensis) possessing these compounds at three concentrations: 50, 100 and 200 ppm were evaluated in controlling the mycelial growth, spore germination and germ tube elongation of B. cinerea. All treatments except savory (annual) essential oil at 50 ppm showed significant differences with the control in inhibiting the mycelial growth as well as spore germination and germ tube elongation of B. cinerea (p=0.01). It was also noted that wild marjoram at 100 ppm and wild savory (perennial) essential oils at 200 ppm could completely (100%) inhibit the growth of the fungus. Essential oils from wild marjoram and wild savory had higher antifungal activity than annual savory. Their suitable formulations could be prepared and used as safe alternatives for controlling moulds of horticultural products during storage. The Agriculturists 2018; 16(2) 15-24

scholarly journals EslB is required for cell wall biosynthesis and modification in Listeria monocytogenes

2020 ◽  
Author(s):  
Jeanine Rismondo ◽  
Lisa M. Schulz ◽  
Maria Yacoub ◽  
Ashima Wadhawan ◽  
Michael Hoppert ◽  
...  
Keyword(s):  
Cell Wall ◽  
Cell Division ◽  
Listeria Monocytogenes ◽  
Abc Transporter ◽  
Cell Lysis ◽  
Growth Conditions ◽  
Cell Wall Integrity ◽  
Growth Defect ◽  
Cell Wall Biosynthesis ◽  
High Concentrations

Lysozyme is an important component of the innate immune system. It functions by hydrolysing the peptidoglycan (PG) layer of bacteria. The human pathogen Listeria monocytogenes is intrinsically lysozyme resistant. The peptidoglycan N-deacetylase PgdA and O-acetyltransferase OatA are two known factors contributing to its lysozyme resistance. Furthermore, it was shown that the absence of components of an ABC transporter, here referred to as EslABC, leads to reduced lysozyme resistance. How its activity is linked to lysozyme resistance is still unknown. To investigate this further, a strain with a deletion in eslB, coding for a membrane component of the ABC transporter, was constructed in L. monocytogenes strain 10403S. The eslB mutant showed a 40-fold reduction in the minimal inhibitory concentration to lysozyme. Analysis of the PG structure revealed that the eslB mutant produced PG with reduced levels of O-acetylation. Using growth and autolysis assays, we show that the absence of EslB manifests in a growth defect in media containing high concentrations of sugars and increased endogenous cell lysis. A thinner PG layer produced by the eslB mutant under these growth conditions might explain these phenotypes. Furthermore, the eslB mutant had a noticeable cell division defect and formed elongated cells. Microscopy analysis revealed that an early cell division protein still localized in the eslB mutant indicating that a downstream process is perturbed. Based on our results, we hypothesize that EslB affects the biosynthesis and modification of the cell wall in L. monocytogenes and is thus important for the maintenance of cell wall integrity. IMPORTANCE The ABC transporter EslABC is associated with the intrinsic lysozyme resistance of Listeria monocytogenes. However, the exact role of the transporter in this process and in the physiology of L. monocytogenes is unknown. Using different assays to characterize an eslB deletion strain, we found that the absence of EslB not only affects lysozyme resistance, but also endogenous cell lysis, cell wall biosynthesis, cell division and the ability of the bacterium to grow in media containing high concentrations of sugars. Our results indicate that EslB is by a yet unknown mechanism an important determinant for cell wall integrity in L. monocytogenes.

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