A procedure has been developed for the purification of 3-dehydroquinase from Escherichia coli. Homogeneous enzyme with specific activity 163 units/mg of protein was obtained in 19% overall yield. The subunit Mr estimated from polyacrylamide-gel electrophoresis in the presence of sodium dodecyl sulphate was 29,000. The native Mr, estimated by gel permeation chromatography on Sephacryl S-200 (superfine) and on TSK G3000SW, was in the range 52,000-58,000, indicating that the enzyme is dimeric. The catalytic properties of the enzyme have been determined and shown to be very similar to those of the biosynthetic 3-dehydroquinase component of the arom multifunctional enzyme of Neurospora crassa.

The limited fossil fuel prompts the prospecting of various unconventional energy sources to take over the traditional fossil fuel energy source. In this respect the use of hydrogen gas is an attractive alternate source. Attributed by its numerous advantages including those of environmentally clean, efficiency and renew ability, hydrogen gas is considered to be one of the most desired alternate. Cyanobacteria are highly promising microorganism for hydrogen production. In comparison to the traditional ways of hydrogen production (chemical, photoelectrical), Cyanobacterial hydrogen production is commercially viable. This review highlights the basic biology of cynobacterial hydrogen production, strains involved, large-scale hydrogen production and its future prospects. While integrating the existing knowledge and technology, much future improvement and progress is to be done before hydrogen is accepted as a commercial primary energy source.

The lysine residues involved in Schiff-base formation at the active sites of both the 3-dehydroquinase component of the pentafunctional arom enzyme of Neurospora crassa and of the monofunctional 3-dehydroquinase of Escherichia coli were labelled by treatment with 3-dehydroquinate in the presence of NaB3H4. Radioactive peptides were isolated by h.p.l.c. following digestion with CNBr (and in one case after further digestion with trypsin). The sequence established for the N. crassa peptide was ALQHGDVVKLVVGAR, and that for the E. coli peptide was QSFDADIPKIA. An amended nucleotide sequence for the E. coli gene (aroD) that encode 3-dehydroquinase is also presented, along with a revised alignment of the deduced amino acid sequences for the biosynthetic enzymes.

Mangroves are climax formation of hydrohalophytes inhabiting estuarine or marine salt marshes in the tropics and subtropics. As a terrestrial plant community inhabiting tidally inundated estuarine or marine sediments, mangroves show considerable adaptation to salinity, water-logging and nutrient stress. Thirty-one species of mangrove and mangrove associates and 23 species of transported flora, belonging to 25 families at four physiographic stages of succession of the mangrove plant community at the terminal part of the Ganges river estuary in India were examined for arbuscular mycorrhizal (AM) root association. Dominant members of the mangrove plant community were all AM, mostly with 'Paris' type structures. Many of the known non-mycotrophic plant families, except the Cyperaceae, also showed AM association, with intracellular hyphae and vesicles as the most discernible endophyte structures. Intensity of AM colonization varied both with the species and situations of their occurrence, being more intense and also more extensive in less saline dry ridge mangroves than in more saline formative and developed swamp mangroves. Introduced exotic trees on the ridges and embankments were infected by AM, but less than the declining mangroves in the same location. Seven species of AM fungi in common with those of the upstream mesophytic plants were isolated from root-free rhizosphere soils of the mangroves, three of which predominated in root association. These species, individually and as mixtures, infected roots of salinity tolerant herbs and trees in both locational silt and upstream alluvial soil with obvious improvements in their biomass yield and phosphorus nutrition. AM infective potential of root-free rhizosphere soils of the dominant members of the mangrove community were negatively related to salinity level of the sediment soil of the successional stages. The evidences of AM association of mangroves and other salt marsh plants obtained here and those reported elsewhere are discussed.

The enzyme 3-dehydroquinase was purified in milligram quantities from an overproducing strain of Escherichia coli. The amino acid sequence was deduced from the nucleotide sequence of the aroD gene and confirmed by determining the amino acid composition of the overproduced enzyme and its N-terminal amino acid sequence. The complete polypeptide chain consists of 240 amino acid residues and has a calculated subunit Mr of 26,377. Transcript mapping revealed that aroD is a typical monocistronic gene.