lithium-chloride and indoleacetic-acid

lithium-chloride has been researched along with indoleacetic-acid* in 3 studies

Other Studies

3 other study(ies) available for lithium-chloride and indoleacetic-acid

ArticleYear
Alteration of growth and gravitropic response of maize roots by lithium.
    Gravitational and space biology bulletin : publication of the American Society for Gravitational and Space Biology, 2005, Volume: 18, Issue:2

    Topics: Cytoplasm; Gravitropism; Indoleacetic Acids; Lithium; Lithium Chloride; Phosphorylation; Plant Growth Regulators; Plant Proteins; Plant Root Cap; Second Messenger Systems; Zea mays

2005
Differential accumulation of transcripts for ACC synthase and ACC oxidase homologs in etiolated mung bean hypocotyls in response to various stimuli.
    Molecules and cells, 1998, Jun-30, Volume: 8, Issue:3

    Ethylene can be produced by a variety of developmental and environmental factors such as ripening, the plant hormone auxin, and mechanical wounding via a biosynthetic pathway including AdoMet synthase, ACC synthase, and ACC oxidase steps. ACC synthase and ACC oxidase are known to be encoded by multigene families, and are believed to be differentially expressed in response to various stimuli. In mung bean, ACC synthase is encoded by 7 genes, ACS1, ACS2 ACS3, ACS4, ACS5, ACS6, and ACS7, and ACC oxidase by 2 genes, ACO1 and ACO2. In this study, was have investigated differential accumulation of transcripts for ACC synthase and ACC oxidase homologs in etiolated mung bean hypocotyls under various conditions by the semiquantitative RT-PCR method. Primers which can specifically bind and amplify each cDNAs of ACS1, ACS2, ACS3, ACS4, ACS5, ACS6, ACS7, and ACO1, and ACO2 were designed and used to monitor the responses to various stimuli. Transcripts of ACO1 and ACO2 were accumulated constitutively in the hypocotyl segments even without andy treatment. After cold treatment on intact plant, transcripts of ACS5, ACS6, and ACS7 were accumulated in the hypocotyl segments. We also found the excision of hypocotyl segments and incubation in a buffer solution, a typical way of chemical treatments to hypocotyl segments, lowered the level of ACO2 transcripts with little change of the level of ACO1 transcripts. In response to incubation with IAA (0.1 mM) of excised hypocotyl segments, transcripts of ACS1, ACS6, and ACS7 were accumulated and the level of ACO2 transcripts was increased. Transcripts of ACS1, ACS2, ACS3, ACS5, ACS6 and ACS7 were induced by incubation with OGA (50 micrograms/ml), while the transcripts of ACS4 were accumulated and the level of ACO2 transcripts was increased by incubation with 1 mM LiCl. Our results strongly suggest that all seven ACC synthase genes and two ACC oxidase genes must be active and each gene is differentially regulated by a different subset of the inducing factors.

    Topics: Adjuvants, Immunologic; Amino Acid Oxidoreductases; Cold Temperature; DNA Primers; Enzyme Induction; Fabaceae; Gene Expression Regulation, Developmental; Gene Expression Regulation, Enzymologic; Gene Expression Regulation, Plant; Hypocotyl; Indoleacetic Acids; Lithium Chloride; Lyases; Multigene Family; Oligosaccharides; Pectins; Plant Growth Regulators; Plants, Medicinal; Polymerase Chain Reaction; RNA, Plant; Sensitivity and Specificity; Sequence Homology, Amino Acid; Stimulation, Chemical; Transcription, Genetic; Transcriptional Activation; Tromethamine

1998
Anaerobiosis and plant growth hormones induce two genes encoding 1-aminocyclopropane-1-carboxylate synthase in rice (Oryza sativa L.).
    Molecular biology of the cell, 1993, Volume: 4, Issue:4

    The plant hormone ethylene is believed to be responsible for the ability of rice to grow in the deepwater regions of Southeast Asia. Ethylene production is induced by hypoxia, which is caused by flooding, because of enhanced activity of 1-aminocyclopropane-1-carboxylic acid (ACC) synthase, the key enzyme in the ethylene biosynthetic pathway. We have cloned three divergent members, (OS-ACS1, OS-ACS2, and OS-ACS3), of a multigene family encoding ACC synthase in rice. OS-ACS1 resides on chromosome 3 and OS-ACS3 on chromosome 5 in the rice genome. The OS-ACS1 and OS-ACS3 genes are induced by anaerobiosis and indoleacetic acid (IAA) + benzyladenine (BA) + LiCl treatment. The anaerobic induction is differential and tissue specific; OS-ACS1 is induced in the shoots, whereas OS-ACS3 is induced in the roots. These inductions are insensitive to protein synthesis inhibitors, suggesting that they are primary responses to the inducers. All three genes are actually induced when protein synthesis is inhibited, indicating that they may be under negative control or that their mRNAs are unstable. The OS-ACS1 gene was structurally characterized, and the function of its encoded protein (M(r) = 53 112 Da, pI 8.2) was confirmed by expression experiments in Escherichia coli. The protein contains all eleven invariant amino acid residues that are conserved between aminotransferases and ACC synthases cloned from various dicotyledonous plants. The amino acid sequence shares significant identity to other ACC synthases (69-34%) and is more similar to sequences in other plant species (69% with the tomato LE-ACS3) than to other rice ACC synthases (50-44%). The data suggest that the extraordinary degree of divergence among ACC synthase isoenzymes within each species arose early in plant evolution and before the divergence of monocotyledonous and dicotyledonous plants.

    Topics: Adenine; Amino Acid Sequence; Anaerobiosis; Base Sequence; Benzyl Compounds; Chlorides; Cycloheximide; Gene Expression Regulation; Genomic Library; Indoleacetic Acids; Kinetin; Lithium; Lithium Chloride; Lyases; Molecular Sequence Data; Multigene Family; Nucleic Acid Hybridization; Oryza; Plant Growth Regulators; Polymerase Chain Reaction; Purines; Transcription, Genetic

1993