植物生理与分子生物学学报最新文献

RPR1 (rice probenazole-responsive) is a rice gene, the expression of which is responsive to probenazole (PBZ), a synthetic compound that may act as a plant defense activator. It has been shown that RPR1 gene may be involved in disease resistance responses. In this study, a series of amplified fragments from the rice RPR1 promoter region, including 2,416 bp, 1,574 bp, 819 bp, 568 bp and 208 bp fragments upstream to the ATG translation start site, were prepared and linked to the coding region of beta-glucuronidase (GUS) gene. Analysis of GUS gene transient expression in rice calli demonstrated that the 568 bp fragment was sufficient for probenazole responsiveness. Analysis of GUS gene stable expression in Arabidopsis thaliana indicated that the 2,416 bp and 1,574 bp fragments drove GUS expression only in shoot apical meristem and petiole. Identification of these PBZ-responsive fragments provides a basis on which PBZ-inducible gene regulatory systems can be constructed for experimental analysis of gene expression and for field application.

This review introduces the pressure probe technique that was originally designed to detect the turgor of a giant algal cell, then adapted to measure the turgor and other water-relations parameters of higher plants, and now has developed into a diverse tool on researches of plant physiology and eco-physiology. This technique can be used to measure in situ the permeability of cell membranes to water and solutes at the resolution of single cells, and hence is a useful tool to study function and regulation of water channels (aquaporins) of intact plant cells. The recently developed xylem-pressure probe technique is the only way to directly measure the negative pressure in xylem conduits. In this review we introduce the basic principles and the theoretical backgrounds underlying the pressure probe. Finally some important achievements and applications of the pressure probe in studies of plant water relations are reviewed and discussed.

Using high-yielding hybrid rice 'Liangyoupeijiu' (LYP9) and hybrid rice 'Shanyou 63' (SY63) as the experimental materials and using (14)C radio-autography, the photosynthetic capacities and distribution of photosynthates in flag leaf blades and sheaths of LYP9 were studied. The results showed that net photosynthetic rates (Pn) of the flag leaf blades and sheaths of LYP9 were much higher than those of SY63; the light transmissivity rates (LT) measured at the medium height of the flag leaf sheaths and the penultimate leaf sheaths were also significantly higher than those of SY63. The incipient activities, total activities and activation percentages of Rubisco in the flag leaf blade and sheath of LYP9 were all higher than those of SY63. The photosynthate transport rate in the sheaths of LYP9, and the quantity of photosynthate transported to the spikes and transformed to economic yield of LYP9 were all higher than those of SY63. The photosynthates produced by the sheaths were mainly transported to spike to make a certain contribution (about 15%) to yield.

The effects of exogenous nitric oxide donor sodium nitroprusside (SNP) on substance metabolism of Ginkgo biloba leaves under drought stress were studied. The results showed that 250 micromol/L SNP (Fig.2) treatment under 35% relative soil water content (RSWC) stress (Fig.1) raised remarkably soluble sugar content (Fig.3), proline content (Fig.4), phenylalanine ammonia lyase (PAL) activity (Fig.5), flavonoids (Fig.6) and ginkgolides content (Fig.7) of G. biloba leaves. Hemoglobin, used as NO scavenger, counteracted the effects of SNP in raising the soluble sugar (Fig.3), proline (Fig.4), flavonoid (Fig.6), ginkgolide content (Fig.7) and PAL activities (Fig.5), which indicates that the effects of sodium nitroprusside were through the nitric oxide released from sodium nitroprusside. We propose from these results that the roles of flavonoids and ginkgolides are the same as those of soluble sugars and proline under drought stress. NO may alleviate the damage caused by drought stress through raising soluble sugar, proline, flavonoid and ginkgolide content.

Manganese (Mn) is an essential micronutrient throughout all stages of plant development. Mn plays an important role in many metabolic processes in plants. It is of particular importance to photosynthetic organisms in the chloroplast of which a cluster of Mn atoms at the catalytic centre function in the light-induced water oxidation by photosystem II, and also function as a cofactor for a variety of enzymes, such as Mn-SOD. But excessive Mn is toxic to plants which is one of the most toxic metals in acid soils. The knowledge of Mn(2+) uptake and transport mechanisms, especially the genes responsible for transition metal transport, could facilitate the understanding of both Mn tolerance and toxicity in plants. Recently, several plant genes were identified to encode transporters with Mn(2+) transport activity, such as zinc-regulated transporter/iron-regulated transporter (ZRT/IRT1)-related protein (ZIP) transporters, natural resistance-associated macrophage protein (Nramp) transporters, cation/H(+) antiporters, the cation diffusion facilitator (CDF) transporter family, and P-type ATPase. In addition, excessive Mn frequently induces oxidative stress, then several defense enzymes and antioxidants are stimulated to scavenge the superoxide and hydrogen peroxide formed under stress. Mn-induced oxidative stress and anti-oxidative reaction are very important mechanisms of Mn toxicity and Mn tolerance respectively in plants. This article reviewed the transporters identified as or proposed to be functioning in Mn(2+) transport, Mn toxicity-induced oxidative stress, and the response of antioxidants and antioxidant enzymes in plants to excessive Mn to facilitate further study. Meanwhile, basing on our research results, new problems and views are brought forward.

By observing the photosynthetic responses of leaves to changes in light intensity and CO(2) concentration it was found that among the more than 50 plant species examined 32 species and 25 species showed respectively the V pattern and L pattern of the photosynthetic response to light intensity transition from saturating to limiting one (Figs.1 and 2 and Table 1). The pattern of photosynthetic response to light intensity transition is species-dependent but not leaf developmental stage-dependent (Fig.3). The species-dependence was not related to classification in taxonomy because the photosynthetic response might display the two different patterns (V and L) in plants of the same family, for example, rice and wheat (Gramineae), soybean and peanut (Leguminosae). It seemed to be related to the pathway of photosynthetic carbon assimilation because all of the C(4) plants examined (maize, green bristlegrass and thorny amaranth) displayed the L pattern. It might be related to light environment where the plants originated. The V pattern of photosynthetic response to light intensity transition was often observed in some plants grown in shade habitats, for example, sweet viburnum and Japan fatsia, while the L pattern was frequently observed in those plants grown in sunny habitats, for example, ginkgo and cotton. Furthermore, the ratio of electron transport rate to carboxylation rate in vivo measured at limiting light was far higher in the V pattern plants (mostly higher than 10) than in the L pattern plants (mostly lower than 5), but the ratio measured at saturating light had no significant difference between the two kinds of plants (Table 2). These results can be explained in part by that the V pattern plant species have larger light-harvesting complex (LHCII) and at saturating light the reversible dissociation of some LHCIIs from PSII reaction center complex occurs. The pattern of photosynthetic response to light intensity transition and the ratio of electron transport rate to carboxylation rate in vivo measured at limiting light can probably be used as a criterion to distinguish sun plants from shade plants. In the observation of photosynthetic response to light intensity transition the use of saturating light is very important because using non-saturating light can form an artifact, which leads to incorrect conclusion (Fig.4).

The sources of nitric oxide (NO) production in response to abscisic acid (ABA) and the role of NO in ABA-induced hydrogen peroxide (H(2)O(2)) accumulation and subcellular antioxidant defense in leaves of maize (Zea mays L.) plants were investigated. ABA induced increases in generation of NO and activity of nitric oxide synthase (NOS) in maize leaves. Such increases were blocked by pretreatment with each of the two NOS inhibitors. Pretreatments with a NO scavenger or NR inhibitors inhibited ABA-induced increase in production of NO, but did not affect the ABA-induced increases in activity of NOS, indicating that ABA-induced NO production originated from sources of NOS and NR. ABA- and H(2)O(2)-induced increases in expression of the antioxidant genes superoxide dismutase 4 (SOD4), cytosolic ascorbate peroxidase (cAPX), and glutathione reductase 1 (GR1) and the activities of the chloroplastic and cytosolic antioxidant enzymes were arrested by pretreatments with the NO scavenger, inhibitors of NOS and NR, indicating that NO is involved in the ABA- and H(2)O(2)-induced subcellular antioxidant defense reactions. On the other hand, NO donor sodium nitroprusside (SNP) reduced accumulation of H(2)O(2) induced by ABA, and c-PTIO reversed the effect of SNP in decreasing the accumulation of H(2)O(2). SNP induced increases in activities of subcellular antioxidant enzymes, and the increases were substantially prevented from occurring by the pretreatment with c-PTIO. These results suggest that ABA induces production of H(2)O(2) and NO, which can up-regulate activities of the subcellular antioxidant enzymes, to prevent overproduction of H(2)O(2) in maize plants. There is a negative feedback loop between NO and H(2)O(2) in ABA signal transduction in maize plants.

LTR-retrotransposons are genetic elements having the direct long terminal repeats (LTRs). It can move via an RNA intermediate within genomes and is an important fraction of eukaryote genomes. Low-energy N(+) ion beam promoted the transcription of the copia-retransposons in those wheat (cv. 'Zhoumai 16', which were radiated and allowed to grow for 24 h and 48 h from the planting. Relative expression ratio of the copia-retransposons was elevated in different degrees (with a max 40 fold) in wheat plants treated with different doses of N(+) beam, comparing to that in the controls. The molecule markers of the IRAP and REMAP to the DNA isolated from the 14-d leaves of wheat plants treated with the low-energy N(+) beam showed that the transposition of some copia-retransposons was re-activated. The enhanced transcription of the copia-retransposons in wheat could weaken or enhance the expression of their nearby genes. The transposition of the retrotransposon in genome can change the primary structure of the functional DNA fragments of chromosomes, and it can also be visualized as the appearance of a new phenotype of plants. In the mid 1980s, the biological effects of low-energy ion beam were recognized and demonstrated experimentally. Hence, it suggests that the enhanced transcription and the re-activated transposition of the retrotransposons are partially attributed to the biological effect of low-energy ion beam.

Cassin, the new gene of ribosome-inactivating protein (RIP) isolated from Cassia occidentalis, was inserted into expression vector pBI121 to produce plant expression vector pBI121-cassin (Figs.1, 2). pBI121-cassin was introduced into tobacco cultivar 'K326' by the Agrobacteriurm tumefaciens transformation method and more than 100 independent transformants were obtained. Southern blot hybridization analysis showed that a single gene locus was inserted into the chromosome of the transgenic tobacco lines (Fig.5) and PCR analysis of segregation population of progeny indicated that the inheritance of transgene was dominant in transgenic lines (Fig.4, Table 1). Results of RT-PCR and Northern blot hybridization analysis showed that transgene could be transcribed correctly (Figs.5, 6) . Three self-pollination lines of transgenic T(1) and T(2) were challenged with TMV at different concentration titers by mechanical inoculation. The transgenic lines exhibited different levels of resistance to TMV with the nontransgenic plants. After both titers of TMV concentration were inoculated, transgenic lines were considered as the highly resistant type with a delay of 4-13 d in development of symptoms and 10%-25% of test plants were infected, while nontransgenic control plants were susceptible typical symptoms on the newly emerged leaves (Table 2). One T(2) line, T(2)-8-2-1, was regarded as an immune type because it did not show any symptoms during 70 d and all plants were shown to be virus free by ELISA tests.

Cucumber seedlings were drought-stressed or inoculated with Pseudoperonospora cubensis. After 3 or 6 d the intercellular fluids of treated cucumber leaves were extracted and analyzed. Protein contents increased after pathogen inoculation and a 27-kD protein was found in intercellular fluids (Figs.1, 7). Both 27 kD proteins were purified from the intercellular fluids of cucumber leaves after drought stress or pathogen inoculation by SDS-PAGE and electro-elution protocol respectively (Fig.2, 3). Purified proteins from drought-stressed and P. cubensis infected seedlings were analyzed by MALDI-TOF MS and their peptide mass fingerprinting (PMF) results were obtained (Figs.4, 5). The PMF results were compared with protein database using the software Profound. The results show that the 27 kD proteins from seedlings after drought stress and after P. cubensis infection were the same protein, i.e. an acidic chitinase (Tables 1, 2; Fig.6). The activities of chitinase in the intercellular fluids of cucumber leaves after pathogen inoculation and in those drought stress were also analyzed. Results showed that both treatments induced the increase in chitinase activity (Fig.8), which indicated that chitinase may be involved in the protection of cucumber plant against both pathogen attack and water stress.