Ultrastructure of thick-walled hyphae of Glomus fasciculatum in old roots of white clover (Trifolium repens)

1984 ◽  
Vol 62 (2) ◽  
pp. 262-271 ◽  
Author(s):  
Loon Lui Lim ◽  
A. L. J. Cole ◽  
B. A. Fineran

Transmission electron microscopy reveals many thick-walled intercellular and intracellular arbuscular trunk hyphae in old roots of white clover. Wall thickness varies among hyphae, from those enclosed by only a primary wall to those in which various layers of secondary wall material occur. The total thickness of the wall usually lies between 1 and 2 μm. The secondary wall shows a lamellar organization and occasionally may almost completely obliterate the protoplast. In some walls, closely packed lamellae form dark-staining bands separated by lighter staining bands of wider spaced lamellae. Cytochemical staining indicates that the primary and secondary walls contain polysaccharide material. Several thick-walled hyphae show broken layers in the outermost regions overlying deeper layers of uninterrupted wall. The ruptured wall appears to have been caused by local expansion of the hypha during the phase of extensive secondary wall thickening. It is suggested that the thick-walled hyphae may provide propagative structures on disintegration of the host cortex. Another hypothesis is that these hyphal walls might provide a pathway for apoplastic transport. Solutions contained in mature tissues of the root might move via the walls for utilization by the endophyte in those regions of the root where the growing hyphae are more active metabolically.

2013 ◽  
Vol 35 (5) ◽  
pp. 655-665 ◽  
Author(s):  
Zeng-Guang WANG ◽  
Guo-Hua CHAI ◽  
Zhi-Yao WANG ◽  
Xian-Feng TANG ◽  
Chang-Jiang SUN ◽  
...  

1977 ◽  
Vol 55 (21) ◽  
pp. 2712-2720 ◽  
Author(s):  
K. L. O'Donnell ◽  
J. J. Ellis ◽  
C. W. Hesseltine ◽  
G. R. Hooper

Light microscopic and scanning and transmission electron microscopic observations were obtained on azygosporogenesis in Mucor azygosporus Benjamin. Terminal gametangia are delimited by centripetally growing septa but plasmodesmata maintain cytoplasmic continuity between the azygophores and gametangia. Warts develop as regularly spaced patches of electron-opaque wall material on, and ultimately within, the inner primary wall. The mature complex azygosporangium wall is composed of (1) remnants of the membranous outer primary wall, (2) the ornamented layer of electron-opaque, stellate, confluent warts, and (3) a fibrillar, electron-opaque, tertiary layer. A homogeneous, hyaline azygospore wall (quaternary layer or endospore) with stellate warts is laid down within the azygosporangium. A comparison of the fine structural aspects of zygosporogenesis and azygosporogenesis in the Mucorales is presented.


2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Jin-Seong Cho ◽  
Min-Ha Kim ◽  
Eun-Kyung Bae ◽  
Young-Im Choi ◽  
Hyung-Woo Jeon ◽  
...  

Abstract Background To create an ideotype woody bioenergy crop with desirable growth and biomass properties, we utilized the viral 2A-meidated bicistronic expression strategy to express both PtrMYB3 (MYB46 ortholog of Populus trichocarpa, a master regulator of secondary wall biosynthesis) and PdGA20ox1 (a GA20-oxidase from Pinus densiflora that produces gibberellins) in wood-forming tissue (i.e., developing xylem). Results Transgenic Arabidopsis plants expressing the gene construct DX15::PdGA20ox1-2A-PtrMYB3 showed a significant increase in both stem fresh weight (threefold) and secondary wall thickening (1.27-fold) relative to wild-type (WT) plants. Transgenic poplars harboring the same gene construct grown in a greenhouse for 60 days had a stem fresh weight up to 2.6-fold greater than that of WT plants. In a living modified organism (LMO) field test conducted for 3 months of active growing season, the stem height and diameter growth of the transgenic poplars were 1.7- and 1.6-fold higher than those of WT plants, respectively, with minimal adverse growth defects. Although no significant changes in secondary wall thickening of the stem tissue of the transgenic poplars were observed, cellulose content was increased up to 14.4 wt% compared to WT, resulting in improved saccharification efficiency of the transgenic poplars. Moreover, enhanced woody biomass production by the transgenic poplars was further validated by re-planting in the same LMO field for additional two growing seasons. Conclusions Taken together, these results show considerably enhanced wood formation of our transgenic poplars, with improved wood quality for biofuel production.


1973 ◽  
Vol 51 (5) ◽  
pp. 1071-1073 ◽  
Author(s):  
J. A. Brushaber ◽  
R. H. Haskins

Two structurally distinct types of secondary wall layers are present in older hyphae in addition to the primary wall. A coarsely fibrous outer wall layer often becomes quite massive and frequently fuses with the outer wall layers of adjacent cells in the formation of hyphal strands. The uneven deposition of this outer layer often produces large verrucosities. The inner secondary wall layer is relatively electron transparent and contains a reticulum of electron-dense lines. The interface of the inner secondary wall with the cytoplasm is often very irregular, and sections of the plasma membrane are frequently overlain by wall material. The outer secondary wall of conidia is composed of an electron-dense material different from that of the outer wall of hyphae. Cells in the multicellular conidia tend to be polyhedral in shape with either very thick primary walls or thin primary walls having a thick inner wall deposit.


2007 ◽  
Vol 48 (12) ◽  
pp. 1659-1672 ◽  
Author(s):  
Chanhui Lee ◽  
Ruiqin Zhong ◽  
Elizabeth A. Richardson ◽  
David S. Himmelsbach ◽  
Brooks T. McPhail ◽  
...  

IAWA Journal ◽  
1995 ◽  
Vol 16 (1) ◽  
pp. 61-68 ◽  
Author(s):  
Uwe Schmitt ◽  
Gudrun Weiner ◽  
Walter Liese

The maturation process of stegmata in the rattan palm Calamus axillaris Becc. was investigated by electron microscopy. Near the apical meristem immature stegmata contain a dense cytoplasm and a centrally located nucleus, but no silica-bodies. Their cell walls, as weIl as those of adjacent fibres, show primary wall-like characteristics. At the third and fourth internode, silica-bodies form within a vacuole of the still immature stegmata; the nucleus becomes displaced towards the parenchyma side of a stegma. Between the fifth and tenth internode, the stegma walls thicken, first at the cell corners adjacent to fibres with subsequent extension to the fibre side. This part of a stegma wall becomes extremely thick and finally envelopes nearly half of the now fully developed silica-body. Its parenchyma side, however, remains free from additional wall material. After completion of wall thickening, the cytoplasm of a stegma degenerates.


2018 ◽  
Vol 115 (27) ◽  
pp. E6366-E6374 ◽  
Author(s):  
Yoichiro Watanabe ◽  
Rene Schneider ◽  
Sarah Barkwill ◽  
Eliana Gonzales-Vigil ◽  
Joseph L. Hill ◽  
...  

In plants, plasma membrane-embedded CELLULOSE SYNTHASE (CESA) enzyme complexes deposit cellulose polymers into the developing cell wall. Cellulose synthesis requires two different sets of CESA complexes that are active during cell expansion and secondary cell wall thickening, respectively. Hence, developing xylem cells, which first undergo cell expansion and subsequently deposit thick secondary walls, need to completely reorganize their CESA complexes from primary wall- to secondary wall-specific CESAs. Using live-cell imaging, we analyzed the principles underlying this remodeling. At the onset of secondary wall synthesis, the primary wall CESAs ceased to be delivered to the plasma membrane and were gradually removed from both the plasma membrane and the Golgi. For a brief transition period, both primary wall- and secondary wall-specific CESAs coexisted in banded domains of the plasma membrane where secondary wall synthesis is concentrated. During this transition, primary and secondary wall CESAs displayed discrete dynamic behaviors and sensitivities to the inhibitor isoxaben. As secondary wall-specific CESAs were delivered and inserted into the plasma membrane, the primary wall CESAs became concentrated in prevacuolar compartments and lytic vacuoles. This adjustment in localization between the two CESAs was accompanied by concurrent decreased primary wall CESA and increased secondary wall CESA protein abundance. Our data reveal distinct and dynamic subcellular trafficking patterns that underpin the remodeling of the cellulose biosynthetic machinery, resulting in the removal and degradation of the primary wall CESA complex with concurrent production and recycling of the secondary wall CESAs.


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