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  • 1
    Publication Date: 2005-01-01
    Print ISSN: 0249-5627
    Electronic ISSN: 1297-9643
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Published by EDP Sciences
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  • 2
    Publication Date: 2002-09-01
    Print ISSN: 0378-1119
    Electronic ISSN: 1879-0038
    Topics: Biology
    Published by Elsevier
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  • 3
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: We are interested in developing a control strategy efficient at the early stages of subterranean development of Orobanche in the inhibition of mannose 6-phosphate reductase (M6PR, EC 1.1.1.224), the key enzyme of mannitol production in the parasite. We examined M6PR gene expression during pre-conditioning, germination, procaulome growth, underground shoot development and emergence of Orobanche ramosa L. attached to tomato roots, the enzyme activity at each of the above stages and the level of stored mannitol in the parasite. A 1120-pb length cDNA isolated by 3′ and 5′RACE was identified as a M6PR sequence by cDNA expression in E. coli and M6PR activity measurement. Only one M6PR gene was detected in O. ramosa following southern blot analysis. M6PR expression, analysed by RT-PCR, was constant from the pre-conditioned seed to the emergence of broomrape, i.e. M6PR expression is constitutive in Orobanche. M6PR activity was also detected in pre-conditioned seeds and attachment to tomato roots resulted in a two-fold increase in enzyme activity during tubercle enlargement and crown root formation. Hexose and mannitol accumulation was strongly enhanced in the attached parasite, with accumulation primarily in the shoot. These results support the prospect of utilizing M6PR inhibitors as early applied herbicides to control this parasite in the early stages of its development.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: In the parasitic plant Striga hermonthica (Del. Benth), asparagine synthesis plays a prominent role in the metabolism of the host-derived nitrogen and in the detoxification process of a steady-state N-excess. Here, we show that asparagine synthetase (EC 6.3.5.4), the primary enzyme involved in asparagine production in plants, is encoded in Striga by a small gene family, with at least two AS genes, including the gene called ShAS related to the small class II Asparagine Synthetase genes. The functionality of ShAS was demonstrated by complementation of an E. coli asn auxotroph mutant and its expression was characterized by semiquantitative RT-PCR. The ShAS expression pattern in plants growing under standard light conditions and in light-grown calli differs from the expression pattern of most plant AS genes since ShAS transcripts accumulated in all the plant organs and this accumulation was not repressed by light. In contrast, ShAS expression was light-induced in mature leaves and in the chlorophyllous calli. The promoter region of ShAS was also sequenced and characterized and displayed various light-responsive, as well as potential sugar-responsive, cis-elements. A correlation between ShAS expression and asparagine synthesis was demonstrated in the illuminated mature leaves by 15N-labelling in vivo experiments. ShAS was also shown to be positively regulated in light-grown calli by C- and N-starvation and was associated with senescence-related protein breakdown. ShAS expression was not repressed by light in haustoria, roots, senescing leaves and inflorescences. These findings show that one or more unknown factors of regulation can override light as the major regulator.
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  • 5
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Heterologous probes representing the entire tobacco chloroplast genome were used to investigate the degree of sequence conservation in the plastid DNA of the totally achlorophyllous plant Lathraea clandestina. Lathraea, a root parasite that grows in the soil, has retained a plastid genome in which the inverted repeat region (IR) is well conserved, with the exception of a short deletion in one of its extremities close to the large single copy region (LSC). Transcription of the 16S rRNA gene located in the IR was demonstrated, suggesting the functionality of the gene expression apparatus. Besides genes for ribosomal proteins (rps7 and rpl20) and for the plastid-encoded subunits of RNA polymerase (rpoA, rpoB, rpoC1 and rpoC2) were amplified by PCR. The single copy regions which contain most of the bioenergetic genes are more divergent than the inverted repeat regions with deleted or strongly altered sequences. This is particularly noticeable in the small one (SSC) which contains, in land plants studied so far, ndh genes for subunits of an NAD(P)H dehydrogenase. Despite some large deletions in the LSC, PCR experiments have shown that some photosynthetis genes, either functional (rbcL) or not (atpB–E) have been maintained. In addition heterologous hybridizations demonstrate that some genes (psaA, psaB, psbC–D) not amplified by PCR have been retained, at least partially. Because the psbA gene, despite having been amplified by PCR, did not map to any location on the Lathraea plastid genome, it is suspected that this sequence has been incorporated in another genome. From these findings we conclude that Lathraea plastid DNA is altered to a lesser extent than in Epifagus, a member of the Orobanchaceae, whilst being very different from Cuscuta reflexa whose plastid DNA (ptDNA) still contains all the photosynthetic genes found in autotrophic angiosperms. The maintenance of an intact rbcL gene might be the reason (or one of the reasons) why Lathraea has retained a plastid genome, even if the function of Rubisco in its amyloplasts remains unclear.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Plant molecular biology 29 (1995), S. 1071-1079 
    ISSN: 1573-5028
    Keywords: atpB gene ; holoparasitic plants ; Lathraea clandestina ; plastid genome ; rbcL gene ; ribulose-1,5-bisphosphate carboxylase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Plastid DNA (ptDNA) regions for the large subunit of ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubiso) (rbcL) and the β-subunit of ATP synthase (atpB) genes of the holoparasite Lathraea clandestina L. were sequenced. These regions were obtained by cloning either a Bam HI endonuclease generated fragment from the Lathraea ptDNA or polymerase chain reaction (PCR) amplified products. The Lathraea ptDNA contains the entire sequence for the rbcL gene which shares 94.5% homology with the Nicotiana tabacum gene, whereas atpB is maintained as a pseudogene. The intergenic region between divergently transcribed rbcL and atpB genes is shorter (758 bp) in L. clandestina plastid genome in comparison with N. tabacum (823 bp), however they have a noticeable similarity, mainly in the rbcL 5′-upstream region. A low level of the rbcL gene transcription was detected whereas no atpB transcripts were found in Lathraea. The plasmid rbcL gene of the hemiparasite Melampyrum pratense and the autotroph Digitalis purpurea both from the Scrophulariaceae were cloned by PCR amplification and then sequenced. The L. clandestina rbcL gene is highly homologous to the M. pratense and D. purpurea genes. The data indicate that the evolution of the plastid atpB-rbcL region was different in parasites from the Scrophulariaceae and Orobanchaceae families.
    Type of Medium: Electronic Resource
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