Cell Wall Layer Induced in Xylem Fibers of Flax Upon Gravistimulation Is Similar to Constitutively Formed Cell Walls of Bast Fibers

In the fibers of many plant species after the formation of secondary cell walls, cellulose-enriched cell wall layers (often named G-layers or tertiary cell walls) are deposited which are important in many physiological situations. Flax (Linum usitatissimum L.) phloem fibers constitutively develop tertiary cell walls during normal plant growth. During the gravitropic response after plant inclination, the deposition of a cellulose-enriched cell wall layer is induced in xylem fibers on one side of the stem, providing a system similar to that of tension wood in angiosperm trees. Atomic force microscopy (AFM), immunochemistry, and transcriptomic analyses demonstrated that the G-layer induced in flax xylem fibers was similar to the constitutively formed tertiary cell wall of bast (phloem) fibers but different from the secondary cell wall. The tertiary cell walls, independent of tissue of origin and inducibility, were twice as stiff as the secondary cell walls. In the gravitropic response, the tertiary cell wall deposition rate in xylem was higher than that of the secondary cell wall. Rhamnogalacturonan I (RG-I) with galactan side chains was a prominent component in cellulose-rich layers of both phloem and xylem flax fibers. Transcriptomic events underlying G-layer deposition in phloem and xylem fibers had much in common. At the induction of tertiary cell wall deposition, several genes for rhamnosyltransferases of the GT106 family were activated in xylem samples. The same genes were expressed in the isolated phloem fibers depositing the tertiary cell wall. The comparison of transcriptomes in fibers with both inducible and constitutive tertiary cell wall deposition and xylem tissues that formed the secondary cell walls is an effective system that revealed important molecular players involved in the formation of cellulose-enriched cell walls.

Threshold for ion movements in wood cell walls below fiber saturation observed by X-ray fluorescence microscopy (XFM)

Diffusion of chemicals and ions through the wood cell wall plays an important role in wood damage mechanisms. In the present work, free diffusion of ions through wood secondary walls and middle lamellae has been investigated as a function of moisture content (MC) and anatomical direction. Various ions (K, Cl, Zn, Cu) were injected into selected regions of 2 μm thick wood sections with a microinjector and then the ion distribution was mapped by means of X-ray fluorescence microscopy with submicron spatial resolution. The MC of the wood was controlled in situ by means of climatic chamber with controlled relative humidity (RH). For all ions investigated, there was a threshold RH below which the concentration profiles did not change. The threshold RH depended upon ionic species, cell wall layer, and wood anatomical orientation. Above the threshold RH, differences in mobility among ions were observed and the mobility depended upon anatomical direction and cell wall layer. These observations support a recently proposed percolation model of electrical conduction in wood. The results contribute to understanding the mechanisms of fungal decay and fastener corrosion that occur below the fiber saturation point.

Zeitliche Einordnung der G-Schicht-Auflagerung in den Prozess der Zellwandbildung bei Zugholzfasern in Zitterpappeln | On the chronology of g-layer formation during cell wall differentiation in tension wood fibres of poplars

The tension wood of some deciduous trees is characterised by fibres that form an additional cell wall layer, the so-called «gelatinous layer» (g-layer). The chronology of g-layer formation in the process of cell wall differentiation and lignification was investigated using two-year old poplars (Populus tremula L.). For this purpose the pinning-method was applied. The results show that the g-layer formation probably takes place at an early stage of secondary wall formation.

MICROFIBRIL ANGLE OF THE S1 CELL WALL LAYER OF NORWAY SPRUCE COMPRESSION WOOD TRACHEIDS

The ultrastructural organization of the outer layer of the secondary wall (i.e. S1 layer) of Norway spruce (Picea abies (L.) Karst.) compression wood tracheids was investigated with emphasis on the microfibril angle. Light microscopy was used to study the orientation of soft rot cavities (viz. microfibril angle) in compression wood tracheids from macerated soft rot degraded wood blocks. In addition, surface and fracture characteristics of compression wood tracheids selected from a thermomechanical pulp were investigated using scanning electron microscopy (SEM). Results showed that the orientation of soft rot cavities varied little between tracheids and the angles were also consistent along the length of individual tracheids. The average S1 microfibril angle in two selected annual rings was 90.0° ± 2.7° and 88.9° ± 2.4° respectively. SEM observations of the compression wood tracheids from the pulp showed distinct fractures between S1 and S2 or within S1 and these fractures were oriented perpendicular to the tracheid axis. It was concluded that the microfibril angle of the S1 layer of compression wood tracheids is higher and less variable than normal wood tracheids. This is considered an adaptation for restraining the compressive forces that act on leaning conifer stems or branches.

Conidial Hydrophobins of Aspergillus fumigatus

ABSTRACT The surface of Aspergillus fumigatus conidia, the first structure recognized by the host immune system, is covered by rodlets. We report that this outer cell wall layer contains two hydrophobins, RodAp and RodBp, which are found as highly insoluble complexes. The RODA gene was previously characterized, and ΔrodA conidia do not display a rodlet layer (N. Thau, M. Monod, B. Crestani, C. Rolland, G. Tronchin, J. P. Latgé, and S. Paris, Infect. Immun. 62:4380-4388, 1994). The RODB gene was cloned and disrupted. RodBp was highly homologous to RodAp and different from DewAp of A. nidulans. ΔrodB conidia had a rodlet layer similar to that of the wild-type conidia. Therefore, unlike RodAp, RodBp is not required for rodlet formation. The surface of ΔrodA conidia is granular; in contrast, an amorphous layer is present at the surface of the conidia of the ΔrodA ΔrodB double mutant. These data show that RodBp plays a role in the structure of the conidial cell wall. Moreover, rodletless mutants are more sensitive to killing by alveolar macrophages, suggesting that RodAp or the rodlet structure is involved in the resistance to host cells.

THE STRUCTURAL ORGANISATION OF THE S1 CELL WALL LAYER OF NORWAY SPRUCE TRACHEIDS

The purpose of the present study was to investigate the ultrastructure of the outer layer of the secondary cell wall (S1) of Norway spruce (Picea abies (L.) Karst.) tracheids with emphasis on microfibril orientation. Several methods were used to obtain complementary results. Macerated tracheids and wood blocks were exposed to degradation by soft rot fungi, different chemicals and mechanical forces. Observations were made using scanning and transmission electron microscopy and light microscopy. It was concluded that the S1 layer is rather homogeneous with respect to microfibril orientation. The major part of the S1 is composed of microfibrils oriented approximately perpendicular to the tracheid axis. Evidence for a crossed fibrillar structure with microfibrils in alternate S- and Z-helices was not obtained. The transition of microfibril orientation from the S1 to the S2 layer appeared abrupt. The transitional/intermediate lamella, where a gradual change in microfibril orientation occurs, should be considered to belong to the outer part of S2.