Recent reports suggest that early sensing of soil water stress by plant roots and the concomitant reduction in stomatal conductance may not be mediated by root-sourced abscisic acid (ABA), but that other xylem-borne chemicals may be the primary stress signal(s). To gain more insight into the role of root-sourced ABA, the timing and location of the expression of genes for key enzymes involved in ABA biosynthesis in Zea mays roots was measured and a comprehensive analysis of root xylem sap constituents from the early to the later stages of water stress was conducted. Xylem sap and roots were sampled from plants at an early stage of water stress when only a reduction in leaf conductance was measured, as well as at later stages when leaf xylem pressure potential decreased. It was found that the majority of ABA biosynthetic genes examined were only significantly expressed in the elongation region of roots at a later stage of water stress. Apart from ABA, sulphate was the only xylem-borne chemical that consistently showed significantly higher concentrations from the early to the later stages of stress. Moreover, there was an interactive effect of ABA and sulphate in decreasing maize transpiration rate and Vicia faba stomatal aperture, as compared to ABA alone. The expression of a sulphate transporter gene was also analysed and it was found that it had increased in the elongation region of roots from the early to the later stages of water stress. Our results support the suggestion that in the early stage of water stress, increased levels of ABA in xylem sap may not be due to root biosynthesis, ABA glucose ester catabolism or pH-mediated redistribution, but may be due to shoot biosynthesis and translocation to the roots. The analysis of xylem sap mineral content and bioassays indicate that the anti-transpirant effect of the ABA reaching the stomata at the early stages of water stress may be enhanced by the increased concentrations of sulphate in the xylem which is also transported from the roots to the leaves.

The unicellular diazotrophic cyanobacterium Cyanothece sp. ATCC 51142 (Cyanothece 51142) is able to grow aerobically under nitrogen-fixing conditions with alternating light-dark cycles or continuous illumination. This study investigated the effects of carbon and nitrogen sources on Cyanothece 51142 metabolism via 13 C-assisted metabolite analysis and biochemical measurements. Under continuous light (50 mmol photons m "2 s "1 ) and nitrogen-fixing conditions, we found that glycerol addition promoted aerobic biomass growth (by twofold) and nitrogenasedependent hydrogen production [up to 25 mmol H 2 (mg chlorophyll) "1 h "1 ], but strongly reduced phototrophic CO 2 utilization. Under nitrogen-sufficient conditions, Cyanothece 51142 was able to metabolize glycerol photoheterotrophically, and the activity of light-dependent reactions (e.g. oxygen evolution) was not significantly reduced. In contrast, Synechocystis sp. PCC 6803 showed apparent mixotrophic metabolism under similar growth conditions. Isotopomer analysis also detected that Cyanothece 51142 was able to fix CO 2 via anaplerotic pathways, and to take up glucose and pyruvate for mixotrophic biomass synthesis. INTRODUCTIONRising concerns about global warming due to the greenhouse effect have renewed research focused on the biological capture of CO 2 . Cyanobacteria have versatile metabolic capabilities, which allow them to grow under autotrophic, heterotrophic and mixotrophic conditions (Bottomley & Van Baalen, 1978;Eiler, 2006;Yang et al., 2002). More importantly, some cyanobacteria can capture solar energy to fix nitrogen and generate H 2 , thereby serving as a source of biofertilizer and biofuel, while simultaneously consuming atmospheric CO 2 (Bernat et al., 2009;Dutta et al., 2005;Fay, 1992;Madamwar et al., 2000;Tamagnini et al., 2007;Tuli et al., 1996). Cyanothece sp. ATCC 51142 (Cyanothece 51142), a unicellular diazotrophic cyanobacterium, is able to grow aerobically under nitrogen-fixing conditions and has been recognized as contributing to the marine nitrogen cycle. The recent sequencing of the Cyanothece 51142 genome and its transcriptional analysis have uncovered the diurnally oscillatory metabolism of the bacterium in alternating light-dark cycles (photosynthesis during the day and nitrogen fixation at night) (Stöckel et al., 2008;Toepel et al., 2008;Welsh et al., 2008). In general, cyanobacteria use spatial or temporal separation of oxygen-sensitive nitrogen fixation and oxygen-evolving photosynthesis as a strategy for diazotrophic growth (Benemann & Weare, 1974;Fay, 1992). Interestingly, Cyanothece 51142 demonstrates simultaneous N 2 fixation and O 2 evolution under continuous-light conditions, though it appears to be unicellular (Colon-Lopez et al., 1997;Huang & Chow, 1986). For example, a recent study of the transcriptional and translational regulation of continuously illuminated Cyanothece has revealed a strong synthesis capability for nitrogenase and circadian expression of 10 % of its genes (Toepel et al., 2008). Furthermore, Cyanothece str...

The central carbon metabolism of cyanobacteria is under debate. For over 50 years, the lack of α-ketoglutarate dehydrogenase has led to the belief that cyanobacteria have an incomplete TCA cycle. Recent in vitro enzymatic experiments suggest that this cycle may in fact be closed. The current study employed (13) C isotopomers to delineate pathways in the cyanobacterium Synechocystis sp. PCC 6803. By tracing the incorporation of supplemented glutamate into the downstream metabolites in the TCA cycle, we observed a direct in vivo transformation of α-ketoglutarate to succinate. Additionally, isotopic tracing of glyoxylate did not show a functional glyoxylate shunt and glyoxylate was used for glycine synthesis. The photomixotrophic carbon metabolism was then profiled with (13) C-MFA under light and carbon-sufficient conditions. We observed that: (i) the in vivo flux through the TCA cycle reactions (α-ketoglutarate → succinate) was minimal (<2%); (ii) the flux ratio of CO2 fixation was six times higher than that of glucose utilization; (iii) the relative flux through the oxidative pentose phosphate pathway was low (<2%); (iv) high flux through malic enzyme served as a main route for pyruvate synthesis. Our results improve the understanding of the versatile metabolism in cyanobacteria and shed light on their application for photo-biorefineries.

Microbes have complex metabolic pathways that can be investigated using biochemistry and functional genomics methods. One important technique to examine cell central metabolism and discover new enzymes is (13)C-assisted metabolism analysis 1. This technique is based on isotopic labeling, whereby microbes are fed with a (13)C labeled substrates. By tracing the atom transition paths between metabolites in the biochemical network, we can determine functional pathways and discover new enzymes. As a complementary method to transcriptomics and proteomics, approaches for isotopomer-assisted analysis of metabolic pathways contain three major steps (2). First, we grow cells with (13)C labeled substrates. In this step, the composition of the medium and the selection of labeled substrates are two key factors. To avoid measurement noises from non-labeled carbon in nutrient supplements, a minimal medium with a sole carbon source is required. Further, the choice of a labeled substrate is based on how effectively it will elucidate the pathway being analyzed. Because novel enzymes often involve different reaction stereochemistry or intermediate products, in general, singly labeled carbon substrates are more informative for detection of novel pathways than uniformly labeled ones for detection of novel pathways(3, 4). Second, we analyze amino acid labeling patterns using GC-MS. Amino acids are abundant in protein and thus can be obtained from biomass hydrolysis. Amino acids can be derivatized by N-(tert-butyldimethylsilyl)-N-methyltrifluoroacetamide (TBDMS) before GC separation. TBDMS derivatized amino acids can be fragmented by MS and result in different arrays of fragments. Based on the mass to charge (m/z) ratio of fragmented and unfragmented amino acids, we can deduce the possible labeled patterns of the central metabolites that are precursors of the amino acids. Third, we trace 13C carbon transitions in the proposed pathways and, based on the isotopomer data, confirm whether these pathways are active (2). Measurement of amino acids provides isotopic labeling information about eight crucial precursor metabolites in the central metabolism. These metabolic key nodes can reflect the functions of associated central pathways. (13)C-assisted metabolism analysis via proteinogenic amino acids can be widely used for functional characterization of poorly-characterized microbial metabolism(1). In this protocol, we will use Cyanothece 51142 as the model strain to demonstrate the use of labeled carbon substrates for discovering new enzymatic functions.

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