Malate synthase from Gossypium hirsutum

Malate synthase was purified 2000-fold from cotyledons of dark-germinated cotton, Gossypium hirsutum. The purified enzyme had a pH optimum of 8.2, and an absolute requirement for a divalent cation. Only glyoxylate and acetyl-CoA served as condensation partners. Results obtained with functional-group directed inhibitors suggest the presence of lysine, tyrosine and histidine residues in the active site. Temperature optimum was 40°, and energy of activation was 3.3 kcal/mol. The MW of cotton malate synthase, determined by rate-zonal density gradient sedimentation, was 750 000. Initial-rate studies indicated Michaelis-Menten kinetics. Inhibition by substrate analogs, plus substrate-interaction kinetics gave results consistent with a sequential bireactant mechanism.     

Antimicrobial terpenoids of Gossypium: 6-methoxygossypol and 6,6′-dimethoxygossypol

The triterpenoid aldehydes, gossypol (1), 6-methoxygossypol (2) and 6,6′-dimethoxygossypol (3); and the sesquiterpenoid aldehydes, hemigossypol (4) and methoxyhemigossypol (5), were isolated from 1-week-old roots of Gossypium hirsutum and G. barbadense and identified. This is the first report of 2 and 3 in nature and of 4 and 5 from healthy roots. Compounds 2 and 3 also constituted 30% of the total terpenoid aldehydes in the seeds of 1 cultivar of G. barbadense, but occurred only in trace quantities in those of G. hirsutum. Spectral data (UV, IR, NMR, MS) and proof of structure for 2 and 3 are presented.     

The induction of normal and teratoid viviparae by a juvenile hormone and kinoprene in two species of aphids

ABSTRACT. Topical application of a juvenile hormone (JH1) and the JH mimic, kinoprene, to short-day, ovipara-producers of Megoura viciae usually leads to the production of oviparous/viviparous intermediate forms in the progeny sequence, in place of the expected sexual females (oviparae). The ovaries of these abnormal forms may contain embryos rather than the haploid yolky eggs of oviparae; 'mixed' ovaries containing both haploid eggs and embryos are also observed. The intermediates range in form from winged (alate) to wingless (apterous). The fully alate individuals usually contain only parthenogenetic ovaries but differ from the naturally occurring alate viviparae in that they are invariably infertile, have fewer antennal sense organs and often bear pheromone releasing glands on the metathoracic tibiae. The hormonally induced production of normal viviparae is difficult in this species but has been achieved by rearing short-day aphids on kinoprene-treated bean plants.
In Aphis fabae similar oviparous/viviparous teratomorphs have been reported and, in addition, single JH1 treatments were shown to induce normal viviparae at the end of the progeny sequence. Multiple applications, beginning prenatally and continuing through the postnatal development of the gynopara (winged ovipara-producer), showed that the numbers of viviparae born were related to the earliness of the treatment and to the dosage. The results are compared with the effect of a switch in photoperiod and discussed in relation to the endocrine control of aphid polymorphism.     

Melatonin in the seasonal response of the aphid Acyrthosiphon pisum

Aphids display life cycles largely determined by the photoperiod.During the warm long-day seasons.most aphid species reproduce by viviparous parthenogenesis.The shortening of the photoperiod in autumn induces a switch to sexual reproduction.Males and sexual females mate to produce overwintering resistant eggs.In addition to this full life cycle(holocycle),there are anholocyelic lineages that do not respond to changes in photoperiod and reproduce continuously by parthenogenesis.The molecular or hormonal events that trigger the scasonal response(i.c,induction of the sexual phenotypes)are still unknown.Although circadian synthesis of melatonin is known to play a key role in vertebrate photoperiodism,the involvement of the circadian clock and/or of the hor-mone melatonin in insect seasonal responses is not so well established.Here we show that melatonin levels in the aphid Acyrthosiphon pisum are significantly higher in holocyclice aphids reared under short days than under long days,while no differences were found between anholoeyelic aphids under the same conditions.We also found that melatonin is localized in the aphid suboesophageal ganglion(SOG)and in the thoracic ganglionic mass(TGM).In analogy to vertcbrates,insect-type arylalkxylamine N-acetyltransferases(i-AANATs)are thought to play a key role in melatonin synthesis.We measured the expression of four I-AANAT genes identified in A.pisum and localized two of them in situ in the insect central nervous systems(CNS).Levels of expression of these genes were compatible with the quantities of melatonin observed.Moreover,like melatonin,expression of these genes was found in the SOG and the TGM.     

Bio-catalyzed coloration of cellulose fibers

Cotton fabrics were dyed with dyes generated in situ by laccase-catalyzed oxidative coupling of the colorless 2,5-diaminobenzenesulfonic acid (2,5-DABSA) and 1-hydroxyphenol (catechol). The enzymatic oxidation of the dye intermediates led to cross-coupling reaction products when the reaction was conducted with an excess of catechol. At least fourfold excess of catechol was necessary to achieve satisfactory dye fixation on cotton. Formation of the same colored product using either an equimolar ratio of the reagents or tenfold excess of catechol was observed. Most probably, homo-molecular reactions predominate over the cross-coupling at equimolar ratio of the precursors, while with an excess of catechol, the cross-coupling occurs in higher yield. The reaction was followed using UV-Vis spectroscopy, HPLC, FTIR and MALDI-TOF MS. A reaction pathway for laccase-induced cross-coupling of catechol and 2,5-DABSA yielding a major colored product was proposed.     

Polyphenols des feuilles de cotonniers et influence sur leur composition d'un choc hydrique ou nutritionnel

A range of phenolic compounds were found in leaves of three cotton species. Water and nutrient stress (sulfur deficiency) both caused a significant decrease in phenolic content. Possible interpretations of the observed phenomena are given.     

An account of the alienicolous morphs of the aphid Patchiella reaumuri (Kaltenbach, 1843) (Homoptera: Aphidoidea)

The alienicolae of Patchiella reaumuri (Kaltenbach), which is heteroecious between Tilia x vulgaris Hayne and roots of Arum species, are here described from material reared on Arum maculatum L. and A. italicum Mill. in 1977. The sexupara morph is also described for the first time from specimens obtained in the same culture. Key couplets are offered whereby this morph can be separated from sexuparae of other British Pemphiginae.     

Additions to the British aphid fauna (Homoptera: Aphidoidea)

Twenty-five species and two subpecies of aphids are listed and dicussed as additions to the Brutish fauna since publication of "Additions and amendment to the Cheack List British aphids" subspecies is described as new to sicence.     

Identification of chalcone synthase genes and their expression patterns reveal pollen abortion in cotton

Chalcone synthase (CHS) is a key enzyme and producing flavonoid derivatives as well play a vital roles in sustaining plant growth and development. However, the systematic and comprehensive analysis of CHS genes in island cotton (G. barbadense) has not been reported yet especially response to cytoplasmic male sterility (CMS). To fill this knowledge gap, a genome-wide investigation of CHS genes were studied in island cotton. A total of 20 GbCHS genes were identified and grouped into five GbCHSs. The gene structure analysis revealed that most of GbCHS genes consisted of two exons and one intron, and 20 motifs were identified. Twenty five pairs duplicated events (12 GbCHS genes) were identified including 23 segmental duplication pairs and two tandem duplication events, representing that GbCHS gene family amplification mainly owned to segmental duplication events and evolving slowly. Gene expression analysis exhibited that the GbCHS family genes presented a diversity expression patterns in various organs of cotton. Coupled with functional predictions and gene expression, the abnormal expression of GbCHS06, 10, 16 and 19 might be associated with pollen abortion of CMS line in island cotton. Conclusively, GbCHS genes exhibited diversity and conservation in many aspects, which will help to better understand functional studies and a reference for CHS research in island cotton and other plants.     

Expansion of MIR482/2118 by a class‐II transposable element in cotton

Some plant microRNA (miRNA) families contain multiple members generating identical or highly similar mature miRNA variants. Mechanisms underlying the expansion of miRNA families remain elusive, although tandem and/or segmental duplications have been proposed. In this study of two tetraploid cottons, Gossypium hirsutum and Gossypium barbadense, and their extant diploid progenitors, Gossypium arboreum and Gossypium raimondii, we investigated the gain and loss of members of the miR482/2118 superfamily, which modulates the expression of nucleotide‐binding site leucine‐rich repeat (NBS‐LRR) disease resistance genes. We found significant expansion of MIR482/2118d in G. barbadense, G. hirsutum and G. raimondii, but not in G. arboreum. Several newly expanded MIR482/2118d loci have mutated to produce different miR482/2118 variants with altered target‐gene specificity. Based on detailed analysis of sequences flanking these MIR482/2118 loci, we found that this expansion of MIR482/2118d and its derivatives resulted from an initial capture of an MIR482/2118d by a class‐II DNA transposable element (TE) in G. raimondii prior to the tetraploidization event, followed by transposition to new genomic locations in G. barbadense, G. hirsutum and G. raimondii. The ‘GosTE’ involved in the capture and proliferation of MIR482/2118d and its derivatives belongs to the PIF/Harbinger superfamily, generating a 3‐bp target site duplication upon insertion at new locations. All orthologous MIR482/2118 loci in the two diploids were retained in the two tetraploids, but mutation(s) in miR482/2118 were observed across all four species as well as in different cultivars of both G. barbadense and G. hirsutum, suggesting a dynamic co‐evolution of miR482/2118 and its NBS‐LRR targets. Our results provide fresh insights into the mechanisms contributing to MIRNA proliferation and enrich our knowledge on TEs.