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Physiology and Molecular Biology of Stress ... - KHAM PHA MOI

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Metabolic Engineering for <strong>Stress</strong> Tolerance<br />

269<br />

3.1.9. Protein Kinase<br />

There is a rapid increase in cytoplasmic Ca 2+ levels in plant cells under various abiotic<br />

stress stimuli. Then, Ca 2+ -dependent protein kinases (CPDK) bring about phosphorylation/<br />

dephosphorylation <strong>of</strong> various proteins, which ultimately mediate Ca 2+ influx<br />

signals (S<strong>and</strong>ers et. al., 1999). Rice plants engineered with altered levels <strong>of</strong> cold- <strong>and</strong><br />

salt-inducible CDPK gene (OsCDPK7) showed high levels <strong>of</strong> salt <strong>and</strong> drought tolerance<br />

on rice plants (Saijo et. al., 2000).<br />

3.1.10. Dehydrins<br />

Plants also synthesize osmoprotectant proteins termed as dehydrins under drought<br />

<strong>and</strong> salinity stress. Overexpression <strong>of</strong> dehydrin HVA1 gene from barley (Xu et. al., 1996)<br />

<strong>and</strong> wheat (Cheng et. al., 2001, 2002) in transgenic rice resulted in resistance towards<br />

salt <strong>and</strong> water deficit stress.<br />

3.2. Other <strong>Stress</strong>es<br />

3.2.1. Anoxia/Hypoxia<br />

Both limited supply <strong>of</strong> water or excessive flooding could cause oxygen deficiency in the<br />

roots. This deficiency triggers ethylene synthesis in the aerial parts <strong>of</strong> the plant <strong>and</strong><br />

produces symptoms, such as chlorosis, senescence <strong>and</strong> ultimately death <strong>of</strong> plants.<br />

Certain plants however, are adapted to low oxygen by maintaining adequate supplies <strong>of</strong><br />

energy <strong>and</strong> sugar to avoid self-poisoning <strong>and</strong> cytoplasmic acidosis (Stearns <strong>and</strong> Glick,<br />

2003).<br />

In general, plants produce ATP <strong>and</strong> NAD by means <strong>of</strong> glycolysis <strong>and</strong> fermentation<br />

rather than using Krebs cycle under oxygen limited conditions. A set <strong>of</strong> enzymes,<br />

such as alcohol dehyrogenase (ADH) <strong>and</strong> pyruvate decarboxylase (PDC) required for<br />

ethanolic <strong>and</strong> lactic acid fermentation is produced due to this anerobic switch (Andrews<br />

et al., 1994). Genes encoding ADH <strong>and</strong> PDC have been cloned <strong>and</strong> described (Bucher<br />

<strong>and</strong> Kuhlemeier, 1993; Umeda <strong>and</strong> Uchimiya, 1994; Hossain et. al., 1996, Quimio et. al.,<br />

2000).<br />

Transgenic tobacco plants overexpressing a bacterial pyruvate decarboxylase<br />

gene showed 20-fold higher pyruvate decarboxylase activity in comparison to the<br />

wild-type (Bucher et. al., 1994, Bucher et. al., 1995, Tadege <strong>and</strong> Kuhlemeier, 1997, Tedege<br />

et. al., 1998). Arabidopsis genes encoding alcohol dehydrogenase, pyruvate decarboxylase<br />

<strong>and</strong> lactate dehydrogenase <strong>and</strong> alanine amino transferase were cloned <strong>and</strong><br />

expressed in Arabidopsis plants (Dennis et. al., 2000). Transgenic cotton plants<br />

overexpressing cotton alcohol dehydrogenase gene displayed 10-30 fold increase in<br />

alcohol dehydrogenase activity <strong>and</strong> ethanol fermentation, whereas the cotton plants

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