Dry weight loss and changes in chemical composition of pine (Pinus kesiya Royle) needles and teak (Tectona grandis L.) leaves during processing in a freshwater lake

The dry weight loss and chemical changes during the process of decomposition of two types of litters viz.; pine (Pinus kesiya Royle) needles and teak (Tectona grandis L.) leaves have been studied in a small freshwater lake using plastic net (1 mm pore size) bags. The results reveal that type of litter and depth of water were the most important factors regulating the rate of decomposition. The percentage composition of cellulose and hemicellulose showed little variation and only a minor fall was noted in their values towards the end of the study period. The lignin percentage increased steadily at all the stations except the deepest station. The sugar and amino acid concentration dropped appreciably during the initial phase and stabilised during later periods. The general trend of change in nitrogen percentage was initial fall - increase - fall - stabilisation at a near original value. The rate of decomposition was faster when compared with similar studies in Canada and Europe.     

Effect of autopolyploidy on quantity and quality of protein in barley

Summary The range and mean protein content of autotetraploids of high-lysine Notch-2 mutants of barley were consistently higher than the diploids in C₃ and C₄ generations of colchicine treated seeds. Amino acid analysis of whole grain meal of diploid Notch-2 and one strain of its autotetraploid revealed differences in the amino acid composition. The proportion of albumin in the diploid and the autotetraploid Notch-2 was higher by 21% and 45% respectively, in comparison to the parent N.P. 113, whereas the glutelin fraction was significantly higher in the autotetraploid. The autotetraploid, with increased glutelin and decreased prolamin, showed no increase in lysine. It is possible that the recessive high-lysine gene may be lacking dosage effect, resulting in no increase in lysine in the autotetraploid, whereas protein content, a polygenically controlled trait, is enhanced due to genome duplication.     

Mass spectral studies of phytosterolins and a ketone from Trianthema pentandra

Mass spectral data of a phytosterolin and its tetraacetate from Trianthema pentandra show that sitosterol-d(+)-glucoside reported earlier¹ was a mixture of sitosteroI-d(+)-glucoside and stigmasterol-d(+)-glucoside. The structure of a ketone has been suggested as nonacos-1-en-4-one, on the basis of physicochemical data. The positions of the double bond and the carbonyl group have been established by MS and NMR data. This is the first report in plants of a C₂₉ ketone with a terminal double bond and carbonyl group at position 4.     

Stereospecific 2'-amination and 2'-chlorination of adenosine by Actinomadura in the biosynthesis of 2'-amino-2'-deoxyadenosine and 2'-chloro-2'-deoxycoformycin

2'-Amino-2'-deoxyadenosine and 2'-chloro-2'-deoxycoformycin (2'-CldCF) are two nucleoside antibiotics produced by Actinomadura. The biosynthesis of these two nucleoside antibiotics has been studied by the addition of [U-14C]adenosine with or without unlabeled adenine to cultures of Actinomadura. By this experimental approach, it is possible to demonstrate that adenosine is the direct precursor for the biosynthesis of 2'-amino-2'-deoxyadenosine and 2'-CldCF. These conclusions are based on the observation that the percentage distribution of 14C in the aglyconic and pentofuranosyl moieties of 2'-amino-2'-deoxyadenosine and 2'-CldCF were similar to the distribution of 14C in the adenine and ribosyl moieties of the [U-14C]adenosine (i.e., 48:52) added to cultures of Actinomadura. Experimentally, the percentage distribution of 14C in the (i) adenine:2-amino-2-deoxy-beta-D-ribofuranose of 2'-amino-2'-deoxyadenosine is 51:49; (ii) 8-(R)-3,6,7,8-tetrahydroimidazo[4,5-d]-[1,3-diazepin-8-o1]:2 -chloro-2- beta-D-ribofuranose of 2'-CldCF is 45:55; and (iii) adenine:ribose of the adenosine isolated from the RNA of Actinomadura is 42:58. Further proof that adenosine is the direct precursor for the biosynthesis 2'-amino-2'-deoxyadenosine and 2'-CldCF was demonstrated by the addition of 75 mumol of unlabeled adenine together with [U-14C]adenosine to nucleoside-producing cultures of Actinomadura. The percentage distribution of 14C in the aglycon and the sugar moieties of 2'-amino-2'-deoxyadenosine and 2'-CldCF were 46:54 and 47:53, respectively; the percentage distribution of 14C in the adenine and ribose moieties of the adenosine isolated from the RNA of Actinomadura was 51:49. These data show that the hydroxyl on C-2' of the ribosyl moiety of adenosine undergoes a replacement by a 2'-amino or a 2'-chloro group to form 2'-amino-2'-deoxyadenosine or 2'-CldCF with retention of stereconfiguration at C-2'. Finally, Actinomadura can utilize inorganic chloride from the medium as demonstrated by the isolation of [36Cl]2'-CldCF following the addition of [36Cl]chloride to the culture medium. Mechanisms for the regioselective modification of the C-2' hydroxyl group and stereospecific insertion of the amino and chloro groups are discussed.     

An analysis of the role of actin during pollen activation leading to germination in pear (Pyrus communis L.): treatment with cytochalasin D

Summary Major stages of actin organization during activation leading to germination of pear (Pyrus communis L.) pollen were disrupted by treatment with 5 g/ml cytochalasin D (CD), and the effects of the drug were monitored with rhodamine-phalloidin staining. CD induced the formation of granules or short rods in the place of the filamentous arrays that occur in normally developing pollen. Filamentous arrays, however, returned upon removal of CD. Pollen incubated directly in CD showed a gradual disappearance of circular actin profiles and their replacement by either granules or, less frequently, short rods. These granules and rods initially had a random distribution in the cell, but with time in CD they became localized at one of the three germination apertures. Pollen was also allowed to reach three stages of microfilament (MF) organization (initial fibrillar arrays, interapertural MFs, and MFs confined beneath a single aperture) prior to being continously exposed to CD. After CD treatment, germination was blocked and the number of cells containing short rods increased, but movement of actin to a single aperture continued. Finally, when pollen at different stages of MF organization was treated with a CD pulse and then transferred to drug-free medium, germination was delayed regardless of the stage of MF organization at the time of treatment. The results indicate that an uninterrupted progression of actin organization is essential for pollen germination, but that movement of actin in the cell is CD-insensitive.     

Prenatal intestinal histology and histochemistry in the goat

The mucosa of the small and large intestine of goat fetuses exhibited villi which had disappeared after the 32.5-cm curved crown rump (CVR) stage. At places, the stratified epithelial lining persisted among the normal columnar epithelium with goblet cells. The concentration of goblet cells increased with age, while the thickness of the epithelium decreased. The crypts of Lieberkühn were tortuous at the base. Brunner's glands appeared at the 14.2-cm CVR stage. Peyer's patches appeared at the 24.5-cm CVR stage in the ileum. The muscularis mucosae differentiated in the large intestine in group II (16.2- to 24.5-cm CVR length) and progressed caudocranially. The striated border of the intestinal epithelium presented with alkaline phosphatase activity; this border and the goblet cells also stained for mucin. Glycogen was demonstrable in the epithelium with greater concentrations in the duodenum and jejunum in group I (11.5- to 14.6-cm CVR length), and in the ileum and large intestine in group III (30.8- to 39.5-cm CVR length).