Evidence for microbial polysaccharide preparations containing polyester substituents

CPMAS 13C-n.m.r. spectroscopy was employed to characterize the composition and solid phase morphology of gellan, welan, rhamsan and NW11. Spectra indicated that commercial preparations of these polysaccharides, which share a similar molecular backbone, contain a non-carbohydrate component exhibiting four inequivalent carbon atoms. Isolation of this component, followed by 13C-n.m.r. in CHCl3 and MS analysis, revealed its structure to be poly(beta-hydroxybutyrate). Evidence is presented which suggests that this polyester may be a covalent adduct to the above polysaccharides, although this cannot be unambiguously determined at this time. Further experimentation is in progress.     

Plant allocation to defensive compounds: interactions between elevated CO2 and nitrogen in transgenic cotton plants

Plant allocation to defensive compounds in response to growthin elevated atmospheric CO₂ in combination with two levels ofnitrogen was examined. The aim was to discover if allocationpatterns of transgenic plants containing genes for defensivechemicals which had not evolved in the species would respondas predicted by the Carbon Nutrient Balance (CNB) hypothesis.Cotton plants (Gossypium hirsutum L.) were sown inside 12 environmentalchambers. Six of them were maintained at an elevated CO₂ levelof 900 µmol mol^-1 and the other six at the current levelof     

Genome size evolution of the extant lycophytes and ferns

Ferns and lycophytes have remarkably large genomes. However, little is known about how their genome size evolved in fern lineages. To explore the origins and evolution of chromosome numbers and genome size in ferns, we used flow cytometry to measure the genomes of 240 species (255 samples) of extant ferns and lycophytes comprising 27 families and 72 genera, of which 228 species (242 samples) represent new reports. We analyzed correlations among genome size, spore size, chromosomal features, phylogeny, and habitat type preference within a phylogenetic framework. We also applied ANOVA and multinomial logistic regression analysis to preference of habitat type and genome size. Using the phylogeny, we conducted ancestral character reconstruction for habitat types and tested whether genome size changes simultaneously with shifts in habitat preference. We found that 2C values had weak phylogenetic signal, whereas the base number of chromosomes (x) had a strong phylogenetic signal. Furthermore, our analyses revealed a positive correlation between genome size and chromosome traits, indicating that the base number of chromosomes (x), chromosome size, and polyploidization may be primary contributors to genome expansion in ferns and lycophytes. Genome sizes in different habitat types varied significantly and were significantly correlated with habitat types; specifically, multinomial logistic regression indicated that species with larger 2C values were more likely to be epiphytes. Terrestrial habitat is inferred to be ancestral for both extant ferns and lycophytes, whereas transitions to other habitat types occurred as the major clades emerged. Shifts in habitat types appear be followed by periods of genomic stability. Based on these results, we inferred that habitat type changes and multiple whole-genome duplications have contributed to the formation of large genomes of ferns and their allies during their evolutionary history.     

2-Hydroxy-7-methoxycadalene. The precursor of lacinilene C 7-methyl ether in Gossypium

Two sesquiterpenoid naphthols, 2,7-dihydroxycadalene and 2-hydroxy-7-methoxycadalene, have been isolated from green and field-dried cotton bracts. These naphthols rapidly autoxidize on silica gel to lacinilene C and lacinilene C 7-methyl ether, respectively. The latter compound has been implicated as a causative of byssinosis. Lacinilene C and its methyl ether derivative isolated from field-dried cotton leaves and bracts were optically active, indicating that the lacinilenes are produced enzymatically from the naphthols. Therefore, bioassays for byssinotic activity using racemic synthetic lacinilene C 7-methyl ether, rather than the naturally occurring optically active compound, must be scrutinized carefully.     

Sesquiterpenoid aldehyde quinones and derivatives in pigment glands of Gossypium

The resistance of Gossypium species to insects is enhanced by compounds in their lysigenous pigment glands. In cultivated cottons, glands in achlorophyllous plant parts contained predominately the terpenoid aldehyde gossypol in G. hirsutum, and gossypol and its methyl and dimethyl ethers in G. barbadense. Glands in young green tissues, however, contained hemigossypolone as the predominant terpenoid aldehyde in G. hirsutum, and a new quinone, hemigossypolone-7-methyl ether, in G. barbadense. As glands aged in green tissues, the sesquiterpenoid quinones were replaced by several C₂₅-terpenoids formed by the Diels-Alder reaction of the quinones with myrcene or trans-β-ocimene. Two C₂₅-terpenoids isolated from G. barbadense, but not G. hirsutum, were the methyl ethers of heliocides H₁ and H₄ and were designated heliocides B₁ and B₄, respectively. A dark red pigment, gossyrubilone, from glands of young leaves of both species is the isopentylimine of hemigossypolone. Similar red imines, formed from sesquiterpenoid quinones and amino acids, resembled the red coloration of the envelope cells surrounding the gland sac. The terpenoid quinones of Gossypium had physical characteristics different from quinones in Bombax which apparently were incorrectly identified as being the same. A survey of the terpenoid quinones and their heliocide derivates in wild Gossypium species and related genera in the Gossypieae showed considerable diversity which may be used for establishing biochemical and phylogenetic relationships.