Morphinan alkaloids in Papaver bracteatum: Biosynthesis and fate

The known metabolic pathway for hydrophenanthrene alkaloids in Papaver somniferum has been examined for occurrence in P. bracteatum, a species reported to contain thebaine but no codeine or morphine. 1,2-Dehydro-reticulinium-[3-¹⁴C] chloride and (±)-reticuline-[3-¹⁴C] were fed to P. bracteatum plants and both were incorporated, the former into reticuline and thebaine and the latter into thebaine, suggesting that thebaine biosynthesis is the same in the two species. Studies of the natural abundance of morphinan alkaloids in P. bracteatum and the results from feeding codeinone-[16-³H] and codeine-[16-³H] indicate that this species can reduce codeinone to codeine but can not perform either of the demethylations to produce codeinone or morphine. Fed thebaine-[16-³H] was substantially metabolized but not by pathways that involved demethylations to either oripavine or northebaine.     

Papaver bracteatum,potential commercial source of codeine

Papaver bracteatum, native to Iran and southern Russia, has been grown successfully in many countries. Research in the northwest United States has confirmed the potential for its commercial production as a source of the alkaloid thebaine. Potential for the chemical conversion of thebaine into codeine, one of man’s most widely used alkaloidal medicinal agents, is reviewed. Economic and social advantages of growing this species over opium poppy (Papaver somniferum) are discussed. The value of the seed oil for cooking and industrial use is considered.     

A rapid quantitative method for the determination of thebaine in Papaver bracteatum

A rapid method enabling a quantitative analysis of thebaine in capsules and latex of Papaver bracteatum has been devised, based on a TLC technique. This method was compared to the commonly used GLC procedure, and highly significant correlation coefficient (r = 0.90) and linear regression were found between the two methods. Values for concentrations to the nearest ±0.25% of the standard spots can be reached by this simple and rapid thebaine determination.     

Bound forms of alkaloids in Papaver somniferum and P. Bracteatum

The polysaccharide fraction of the pericarp and seed of Papaver somniferum were shown to contain bound forms of morphine which were derived from radioactive morphine fed to living plants. Bound forms of codeine, thebaine and some unidentified alkaloid-like compounds were also detected in the pericarp and bound thebaine occurred in the pericarp of Papaver bracteatum. The complexity and molecular weight of the bound alkaloids seemed to increase during ripening, and it is suggested that these substances represent transitional forms in the metabolism and transiocation of morphine from latex to seed.     

Cytochrome P450 3A Enzymes Catalyze the O6-Demethylation of Thebaine,a Key Step in Endogenous Mammalian Morphine Biosynthesis

Morphine, first characterized in opium from the poppy Papaver somniferum, is one of the strongest known analgesics. Endogenous morphine has been identified in several mammalian cells and tissues. The synthetic pathway of morphine in the opium poppy has been elucidated. The presence of common intermediates in plants and mammals suggests that biosynthesis occurs through similar pathways (beginning with the amino acid l-tyrosine), and the pathway has been completely delineated in plants. Some of the enzymes in the mammalian pathway have been identified and characterized. Two of the latter steps in the morphine biosynthesis pathway are demethylation of thebaine at the O³- and the O⁶-positions, the latter of which has been difficult to demonstrate. The plant enzymes responsible for both the O³-demethylation and the O⁶-demethylation are members of the Fe^II/α-ketoglutarate-dependent dioxygenase family. Previous studies showed that human cytochrome P450 (P450) 2D6 can catalyze thebaine O³-demethylation. We report that demethylation of thebaine at the O⁶-position is selectively catalyzed by human P450s 3A4 and 3A5, with the latter being more efficient, and rat P450 3A2. Our results do not support O⁶-demethylation of thebaine by an Fe^II/α-ketoglutarate-dependent dioxygenase. In rat brain microsomes, O⁶-demethylation was inhibited by ketoconazole, but not sulfaphenazole, suggesting that P450 3A enzymes are responsible for this activity in the brain. An alternate pathway to morphine, oripavine O⁶-demethylation, was not detected. The major enzymatic steps in mammalian morphine synthesis have now been identified.     

The alkaloidal constituents of Papaver bracteatum arya II

Seven alkaloids were isolated from Papaver bracteatum Arya II, six of which: thebaine, 14β-hydroxycodeine, codeine, neopine, alpinigenine and protopine, have been previously found to be present in other types of this species. It is the first report of the isolation of O-methylflavinantine from P. bracteatum.     

Biotransformation of (RS)-reticuline and morphinan alkaloids by cell cultures of Papaver somniferum

(RS)-Reticuline was stereospecifically converted to (—)-(S)-scoulerine and (—)-(S)-cheilanthifoline by cell cultures of Papaver somniferum and (—)-(R)-reticuline was recovered as an optical pure compound by racemic resolution. (—)-Codeinone was converted in high yield to (—)-codeine in both cell culture and enzyme preparation, but the other morphinans, thebaine, codeine and morphine, were not metabolized.     

Gene actions for yield and its attributes and their implications in the inheritance pattern over three generations in opium poppy (<Emphasis Type="Italic">Papaver somniferum</Emphasis> L.)

The gene actions for yield and its attributes and their inheritance pattern based on five parameter model have been explored in four single crosses (NBIHT-5 × NBIHT-6, NBIHT-5 × NBMHT-1, NBMHT-1 × NBIHT-6 and NBMHT-2 × NBMHT-1) obtained using thebaine rich pure lines of opium poppy (Papaver somniferum L.) for three consecutive generations. All the traits showed nonallelic mode of interaction, however, dominance effect (h) was more pronounced for all the traits except thebaine and papaverine. The dominance × dominance (l) effects were predominant over additive × additive (i) for all traits in all the four crosses except for papaverine. The seed and opium yield, and its contributing traits inherited quantitatively. The fixable gene effects (d) and (i) were lower in magnitude than nonfixable (h) and (l) gene effects. The estimates of heterosis were also higher in comparison to the respective parents which suggested preponderance of dominance gene action for controlling most of the traits. The phenotypic coefficient of variation was marginally higher than those of genotypic coefficient of variation for all the traits. The traits thebaine, narcotine, morphine and opium yield had high heritability coupled with high genetic advance. The leaf number, branches per plant and stem diameter showed positive correlation with opium and seed yields. The selection of plants having large number of leaves, branches and capsules with bigger size would be advantageous to enhance the yield potential.     

罂粟体内蒂巴因变化规律及水氮耦合对蒂巴因的影响

该文采用HPLC法,分析测定一年生罂粟植株体开花后不同生育期根、茎、叶、果壳中的蒂巴因含量,研究了罂粟体内蒂巴因的变化规律和水氮耦合对蒂巴因的影响。结果表明:一年生罂粟植株体的蒂巴因含量的变化范围在果壳中为1.81%～4.54%,成熟期达到最高;叶片中为0.30%～0.68%,膨大后期最高,采收期最低;根中为0.03%～0.28%,膨大前期最高,采收期最低;茎秆中为0.23%～0.60%,呈递减趋势,采收期最低,茎上、中、下部的蒂巴因含量的变化范围分别为0.42%～0.97%、0.15%～0.60%、0.13%～0.37%。滴灌量和施氮量对一年生罂粟果壳中蒂巴因含量的影响差异显著。罂粟壳质量最佳的水氮偶合条件为I_(130)N_(14),即滴灌量为130 m~3·667 m~(-2),施氮量为14 kg·667 m~(-2)时,蒂巴因含量达最高。     

Radioimmunoassay determination of six opium alkaloids and its application to plant screening

Radioimmunoassay procedures were developed for the independent and specific determination of sub-nmole quantities of (S)- and (R)-reticuline, salutaridine, thebaine, codeine and morphine. Assay parameters for all six poppy alkaloids are given and the synthesis of haptens and tracers in the Ci/mmol range is described. These assays were used to screen herbarium material of 100 Papaver species and to analyse P. somniferum plant populations for alkaloid breeding purposes. The time course of alkaloid appearance during the germination of poppy seeds was also studied.     

N-Demethylation of N-methyl alkaloids with ferrocene

Under Polonovski-type conditions, ferrocene has been found to be a convenient and efficient catalyst for the N-demethylation of a number of N-methyl alkaloids such as opiates and tropanes. By judicious choice of solvent, good yields have been obtained for dextromethorphan, codeine methyl ether, and thebaine. The current methodology is also successful for the N-demethylation of morphine, oripavine, and tropane alkaloids, producing the corresponding N-nor compounds in reasonable yields. Key pharmaceutical intermediates such oxycodone and oxymorphone are also readily N-demethylated using this approach.     

Neodihydrothebaine and bractazonine,two dibenz[d,f]azonine alkaloids of Papaver bracteatum

Two new dibenz[d,f]azonine alkaloids, neodihydrothebaine and bractazonine were isolated from Papaver bracteatum. Their possible biosynthesis from thebaine is discussed. The structures of both new alkaloids are proven by synthesis. An isomeric dibenz[d,f]azonine compound was also prepared.     

Morphine Biosynthesis in Opium Poppy Involves Two Cell Types: Sieve Elements and Laticifers

Immunofluorescence labeling and shotgun proteomics were used to establish the cell type–specific localization of morphine biosynthesis in opium poppy (Papaver somniferum). Polyclonal antibodies for each of six enzymes involved in converting (R)-reticuline to morphine detected corresponding antigens in sieve elements of the phloem, as described previously for all upstream enzymes transforming (S)-norcoclaurine to (S)-reticuline. Validated shotgun proteomics performed on whole-stem and latex total protein extracts generated 2031 and 830 distinct protein families, respectively. Proteins corresponding to nine morphine biosynthetic enzymes were represented in the whole stem, whereas only four of the final five pathway enzymes were detected in the latex. Salutaridine synthase was detected in the whole stem, but not in the latex subproteome. The final three enzymes converting thebaine to morphine were among the most abundant active latex proteins despite a limited occurrence in laticifers suggested by immunofluorescence labeling. Multiple charge isoforms of two key O-demethylases in the latex were revealed by two-dimensional immunoblot analysis. Salutaridine biosynthesis appears to occur only in sieve elements, whereas conversion of thebaine to morphine is predominant in adjacent laticifers, which contain morphine-rich latex. Complementary use of immunofluorescence labeling and shotgun proteomics has substantially resolved the cellular localization of morphine biosynthesis in opium poppy.     

Autonomous cellular differentiation of homoeotic bithorax mutants of Drosophila melanogaster

Various mixtures of imaginal disc cells from wild-type and from homoeotic bithorax mutants have been studied in an in vivo Drosophila cell culture system. These mutants effect specific types of segmental transformations, e.g., bithorax-3 (bx³) transforms the anterior region of the metathorax (MT) into a region resembling the anterior mesothorax (MS), while postbithorax (pbx) transforms the posterior MT into a posterior MS-like region. In cell mixtures, wild-type haltere-disc cells segregate from wild-type wing-disc cells. On the other hand, bx³ and pbx haltere-disc cells integrate with wild-type cells derived from anterior and posterior regions, respectively, of wing discs. The behavior of these and other tested mutants of the bithorax series indicates in all cases studied that (1) the effects of the mutants are cell-autonomous, and (2) cellular affinities are determined by the genetic constitution rather than the segmental origin of the cells.     

Protoplasts of Cosmarium as a Potential Protein Source

Cosmarium turpinii, a fast-growing desmid alga, transforms into protoplasts in 4 h when incubated in a mineral medium + 0.4 M mannitol + 0.5% Cellulysin.     

Measurement of some Benzylisoquinoline Alkaloids in Different Organs of Persian Poppy during Ontogenetical Stages

Papaver bracteatum, a perennial species, has been known as a rich source of thebaine and a potential alternative to Papaver somniferum for the production of codeine and some semisynthetic antagonist drugs. In this study, ion mobility spectrum (IMS) of the root, leaf, bottom part of stem, upper part of stem, capsule wall, petal, and capsule content during developmental stages of P. bracteatum including annual rosette, perennial rosette, bud initiation, pendulous bud, preflowering, and lancing were investigated. The IMS revealed thebaine, papaverine, and noscapine as the major components of the extracted alkaloids. Based on the results of the study it appears that, at least in part, there is a competition among the biosynthesis pathways of papaverine, noscapine, and morphinan alkaloids from a common source . Root and capsule wall were the most potent organs for extraction of thebaine, while lancing stage was the best developmental stage for thebaine exploitation. However, it seems that total biomass of root and capsule wall plays a key role in the final selection of favorite organ. Although papaverine and noscapine in the stem at preflowering stage had the most quantity, significant amounts were found in the capsule wall. In general, total alkaloid content of leaf was lower than the other plant parts.     

Use of Genome Engineering to Create Patient Specific MLL Translocations in Primary Human Hematopoietic Stem and Progenitor Cells

One of the challenging questions in cancer biology is how a normal cell transforms into a cancer cell. There is strong evidence that specific chromosomal translocations are a key element in this transformation process. Our studies focus on understanding the developmental mechanism by which a normal stem or progenitor cell transforms into leukemia. Here we used engineered nucleases to induce simultaneous specific double strand breaks in the MLL gene and two different known translocation partners (AF4 and AF9), which resulted in specific chromosomal translocations in K562 cells as well as primary hematopoietic stem and progenitor cells (HSPCs). The initiation of a specific MLL translocation in a small number of HSPCs likely mimics the leukemia-initiating event that occurs in patients. In our studies, the creation of specific MLL translocations in CD34+ cells was not sufficient to transform cells in vitro. Rather, a variety of fates was observed for translocation positive cells including cell loss over time, a transient proliferative advantage followed by loss of the clone, or a persistent proliferative advantage. These studies highlight the application of genome engineering tools in primary human HSPCs to induce and prospectively study the consequences of initiating translocation events in leukemia pathogenesis.