Stromule

Abstract: One mechanism to enhance global food stocks radically is to introduce C 4 photosynthesis into C 3 crops from warm climates, notably rice. To accomplish this, an understanding of leaf structure and function is essential. The chlorenchyma structure of rice and related warm-climate C 3 grasses is distinct from that of cool temperate C 3 grasses. In temperate C 3 grasses, vacuoles occupy the majority of the cell, while chloroplasts, peroxisomes and mitochondria are pressed against the cell periphery. In rice, 66% of protoplast volume is occupied by chloroplasts, and chloroplasts/stromules cover >95% of the cell periphery. Mitochondria and peroxisomes occur in the cell interior and are intimately associated with chloroplasts/stromules. We hypothesize that the chlorenchyma architecture of rice enhances diffusive CO 2 conductance and maximizes scavenging of photorespired CO 2 . The extensive chloroplast/stromule sheath forces photorespired CO 2 to exit cells via the stroma, where it can be refixed by Rubisco. Deep cell lobing and small cell size, coupled with chloroplast sheaths, creates high surface area exposure of stroma to intercellular spaces, thereby enhancing mesophyll transfer conductance. In support of this, rice exhibits higher mesophyll transfer conductance, greater stromal CO 2 content, lower CO 2 compensation points at warm temperature and less oxygen sensitivity of photosynthesis than cool temperate grasses. Rice vein length per leaf, mesophyll thickness and intercellular space volume are intermediate between those of most C 3 and C 4 grasses, indicating that the introduction of Kranz anatomy into rice may not require radical changes in leaf anatomy; however, deep lobing of chlorenchyma cells may constrain efforts to engineer C 4 photosynthesis into rice.

Abstract: Green fluorescent stroma filled tubules (stromules) emanating from the plastid surface were observed in transgenic plants containing plastid-localized green fluorescent protein (GFP). These transgenic tobacco plants were further investigated by epifluorescence and confocal laser scanning microscopy (CSLM) to identify developmental and/or cell type specific differences in the abundance and appearance of stromules and of plastids. Stromules are rarely seen on chlorophyll-containing plastids in cell types such as trichomes, guard cells or mesophyll cells of leaves. In contrast, they are abundant in tissues that contain chlorophyll-free plastids, such as petal and root. The morphology of plastids in roots and petals is highly dynamic, and plastids are often elongated and irregular. The shapes, size, and position of plastids vary in particular developmental zones of the root. Furthermore, suspension cells of tobacco exhibit stromules on virtually every plastid with two major forms of appearance. The majority of cells show a novel striking 'octopus- or millipede-like' structure with plastid bodies clustered around the nucleus and with long thin stromules of up to at least 40 (micro)m length stretching into distant areas of the cell. The remaining cells have plastid bodies distributed throughout the cell with short stromules. Photobleaching experiments indicated that GFP can flow through stromules and that the technique can be used to distinguish interconnected plastids from independent plastids.

Abstract: A fundamental mystery of plant cell biology is the occurrence of “stromules,” stroma-filled tubular extensions from plastids (such as chloroplasts) that are universally observed in plants but whose functions are, in effect, completely unknown. One prevalent hypothesis is that stromules exchange signals or metabolites between plastids and other subcellular compartments, and that stromules are induced during stress. Until now, no signaling mechanisms originating within the plastid have been identified that regulate stromule activity, a critical missing link in this hypothesis. Using confocal and superresolution 3D microscopy, we have shown that stromules form in response to light-sensitive redox signals within the chloroplast. Stromule frequency increased during the day or after treatment with chemicals that produce reactive oxygen species specifically in the chloroplast. Silencing expression of the chloroplast NADPH-dependent thioredoxin reductase, a central hub in chloroplast redox signaling pathways, increased chloroplast stromule frequency, whereas silencing expression of nuclear genes related to plastid genome expression and tetrapyrrole biosynthesis had no impact on stromules. Leucoplasts, which are not photosynthetic, also made more stromules in the daytime. Leucoplasts did not respond to the same redox signaling pathway but instead increased stromule formation when exposed to sucrose, a major product of photosynthesis, although sucrose has no impact on chloroplast stromule frequency. Thus, different types of plastids make stromules in response to distinct signals. Finally, isolated chloroplasts could make stromules independently after extraction from the cytoplasm, suggesting that chloroplast-associated factors are sufficient to generate stromules. These discoveries demonstrate that chloroplasts are remarkably autonomous organelles that alter their stromule frequency in reaction to internal signal transduction pathways.