The rapid and long-lasting growth of grasses following small falls of rain on stony downs in the arid interior of Australia

Abstract Stony downs consist of grassy areas that alternate with areas that have a substantial stone cover. The stone-covered areas are impermeable, and most rain falling on them runs off, substantially increasing the effective rainfall in adjacent grassy areas. As a result, 20–25 mm of rain on stony downs wetted the soil around the grass to a depth of 140–170 mm and allowed sustained grass response. This is much less than the 35–40 mm of rain required for the same response on red clay or grey clay plains. Grasses respond very rapidly after rain. Some have green shoots the day after rain, and all have responded by the second day. Ephemerals dry off in 4–6 weeks, but most tussock grasses still have some green foliage 8–10 weeks after rain. Deeper rooted tussock grasses remain green for so long because most of the moisture that reaches deeper roots after rain remains there. Most moisture loss is through the soil surface and is recognizable as a drying front that descends through the soil profile. Soil above the drying front is nearly air dry (<5% moisture) while soil below the front has substantial moisture (14–16%). By about a month after rain in summer, the drying front is at a depth of about 80–120 mm. This is near the tips of the roots of ephemeral grasses and the ephemerals then dry off rapidly. Only the tips of the leaves of deep rooted grasses like Mitchell grass (Astrebla spp.) dry off. Their leaves continue to remain mostly green during most of the second month after rain and they do not dry off completely until the third month when the drying front reaches the bottom of the main root system.     

Comparative shotgun proteomic analysis of Clostridium acetobutylicum from butanol fermentation using glucose and xylose

Background

Cytokinin is a plant hormone that plays a crucial role in several processes of plant growth and development. In recent years, major breakthroughs have been achieved in the elucidation of the metabolism, the signal perception and transduction, as well as the biological functions of cytokinin. An important activity of cytokinin is the involvement in chloroplast development and function. Although this biological function has already been known for 50 years, the exact mechanisms remain elusive.

Results

To elucidate the effects of altered endogenous cytokinin content on the structure and function of the chloroplasts, chloroplast subfractions (stroma and thylakoids) from transgenic Pssu-ipt and 35S:CKX1 tobacco (Nicotiana tabacum) plants with, respectively, elevated and reduced endogenous cytokinin content were analysed using two different 2-DE approaches. Firstly, thykaloids were analysed by blue-native polyacrylamide gel electrophoresis followed by SDS-PAGE (BN/SDS-PAGE). Image analysis of the gel spot pattern thus obtained from thylakoids showed no substantial differences between wild-type and transgenic tobacco plants. Secondly, a quantitative DIGE analysis of CHAPS soluble proteins derived from chloroplast subfractions indicated significant gel spot abundance differences in the stroma fraction. Upon identification by MALDI-TOF/TOF mass spectrometry, these proteins could be assigned to the Calvin-Benson cycle and photoprotective mechanisms.

Conclusion

Taken together, presented proteomic data reveal that the constitutively altered cytokinin status of transgenic plants does not result in any qualitative changes in either stroma proteins or protein complexes of thylakoid membranes of fully developed chloroplasts, while few but significant quantitative differences are observed in stroma proteins.