Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Richard J. Robins is active.

Publication


Featured researches published by Richard J. Robins.


Plant Cell Reports | 1986

Secondary product formation by cultures of Beta vulgaris and Nicotiana rustica transformed with Agrobacterium rhizogenes.

John D. Hamill; Adrian J. Parr; Richard J. Robins; Michael J. C. Rhodes

Abstract‘Hairy root’ cultures of Beta vulgaris and Nicotiana rustica were established after roots were induced on plants following infection with Agrobacterium rhizogenes. The transformed cultures of B. vulgaris and N. rustica synthesised their characteristic secondary products, the betalain pigments and nicotine alkaloids respectively, at levels comparable with those of in vivo roots from the same variety. Betalains were entirely retained inside the root tissue. In contrast, a proportion of the nicotine alkaloids was secreted into the medium. The potential of this type of ‘in vitro’ plant tissue culture for the production of valuable plant secondary products is identified and confirmed.


Plant Molecular Biology | 1990

Over-expressing a yeast ornithine decarboxylase gene in transgenic roots of Nicotiana rustica can lead to enhanced nicotine accumulation.

John D. Hamill; Richard J. Robins; Adrian J. Parr; David M. Evans; Judith M. Furze; Michael J. C. Rhodes

Transformed root cultures of Nicotiana rustica have been generated in which the gene from the yeast Saccharomyces cerevisiae coding for ornithine decarboxylase has been integrated. The gene, driven by the powerful CaMV35S promoter with an upstream duplicated enhancer sequence, shows constitutive expression throughout the growth cycle of some lines, as demonstrated by the analysis of mRNA and enzyme activity. The presence of the yeast gene and enhanced ornithine decarboxylase activity is associated with an enhanced capacity of cultures to accumulate both putrescine and the putrescine-derived alkaloid, nicotine. Even, however, with the very powerful promoter used in this work the magnitude of the changes seen is typically only in the order of 2-fold, suggesting that regulatory factors exist which limit the potential increase in metabolic flux caused by these manipulations. Nevertheless, it is demonstrated that flux through a pathway to a plant secondary product can be elevated by means of genetic manipulation.


Planta | 1991

Studies on the biosynthesis of tropane alkaloids in Datura stramonium L. transformed root cultures : 1. The kinetics of alkaloid production and the influence of feeding intermediate metabolites.

Richard J. Robins; Adrian J. Parr; Elizabeth G. Bent; Michael J. C. Rhodes

The factors by which the endogenous regulation of tropane-alkaloid biosynthesis may be effected have been examined in a transformed root culture of Datura stramonium. Pools of intermediates showed a subculture-related maximal accumulation, as did the enzyme activities by which they are synthesised and/or metabolised. The end-products, principally hyoscyamine and apohyoscyamine, in contrast, accumulated steadily in growing cultures. Feeding putrescine, agmatine or tropine did not enhance alkaloid accumulation, but rather may even have resulted in a lowering of hyoscyamine levels. Similarly, feeding precursors for the tropate moiety of hyoscyamine either had no influence or had a detrimental effect on hyoscyamine accumulation. Under some feeding conditions, intermediates in the pathway from N-methylputrescine up to and including tropine accumulated up to 40-fold. Little effect on early intermediates was found, however, when tropinone or tropine were fed. The expression of the enzyme arginine decarboxylase (EC 4.1.1.19) was particularly sensitive to feed-back repression, both by its product agmatine and by more distant pathway intermediates, notably putrescine and tropine. Some diminution of the levels of putrescine N-methyltransferase (EC 2.1.1.53) and N-methylputrescine oxidase, the first committed enzymes of alkaloid biosynthesis, was also seen with tropine, although only at rather high levels. It is concluded that the pathway is not regulated in a simple manner and that (i) the early enzymes of the pathway are at near rate-limiting levels, (ii) there is a major limitation to flux at the level of the esterification of tropine, and (iii) the level of free tropine may be important in determining the flux into and through the tropane pathway.


Plant Cell Reports | 1988

Alkaloid production by transformed root cultures of Catharanthus roseus

Adrian J. Parr; Abigael C. J. Peerless; John D. Hamill; N. J. Walton; Richard J. Robins; M.J.C. Rhodes

Transformed roots of Catharanthus roseus were obtained following infection of detached leaves with Agrobacterium rhizogenes. Roots would not grow in full strength Gamborgs B5 medium but would grow satisfactorily if the medium was diluted to one half strength. Little alkaloid appeared in the growth medium but root tissue contained a high level and wide variety of alkaloids. Ajmalicine, serpentine, vindolinine and catharanthine were prominent components. Vinblastine could also be detected by a combination of HPLC and radioimmunoassay, though at a level of only 0.05μg/g dry weight.


Phytochemistry | 1990

Variation in tropane alkaloid accumulation within the solanaceae and strategies for its exploitation

Adrian J. Parr; J. Payne; John Eagles; Bridget T. Chapman; Richard J. Robins; Michael J. C. Rhodes

Key Word Index-Datum spp.; Hyoscyamus spp.; Scopolia spp.; Solanaceae; identification; accumulation; trans- formed roots; tropane alkaloids; scopolamine; hyoscyamine. - Abstract-Petioles from over 1000 individual plants of the genera Datura, Scopolia and Hyoscyamus were analysed to establish the variation in the levels and patterns of tropane alkaloids which occur between plants. Transformed root cultures were initiated from plants of which analyses suggested extremely high or low alkaloid biosynthetic capacities, or favourable alkaloid patterns. These root cultures were then studied in detail by HPLC, GC and GC-MS. Root cultures showed substantial differences in alkaloid patterns between different species, but the quantitative differences in tropoyl esters of cc-tropine (hyoscyamine plus scopolamine) observed between different lines were less than those seen between plants. This difference is interpreted as to some extent reflecting the influence of transport and storage effects, as well as biosynthetic capacity, in determining alkaloid levels in plant petioles. In addition, there is some indication that the full biosynthetic capacity may not always be expressed in culture. Despite these limitations, the identification of plants showing favourable characteristics still, however, proved a useful first step in the development of scientifically and potentially biotechnologically interesting root cultures.


Biotechnology Letters | 1986

Nicotine production by “hairy root” cultures of Nicotiana rustica: Fermentation and product recovery

Michael J. C. Rhodes; Martin G. Hilton; Adrian J. Parr; John D. Hamill; Richard J. Robins

The production of nicotine by cultures ofNicotiana rustica transformed withAgrobacterium rhizogenes has been examined in a packed bed fermenter as a two-stage batch/continuous-flow system. A substantial proportion of the nicotine synthesised in the batch phase may be subsequently harvested from the medium. The possibility of improving product recovery using macroreticular adsorbents is considered.


Applied Microbiology and Biotechnology | 1986

The stimulation of anthraquinone production by Cinchona ledgeriana cultures with polymeric adsorbents

Richard J. Robins; Michael J. C. Rhodes

SummaryAnthraquinones produced by suspension cultures of Cinchona ledgeriana are released into the medium, which becomes saturated with products late in the growth cycle. When a high affinity polymeric adsorbent, such as the macro-reticular Amberlite XAD-7, is added to the culture the concentration of anthraquinone in the medium is maintained at a low level and production may be stimulated 15-fold, yielding up to 20 mg/1/day. More than 90% of the product is released from the cells. For maximal yields it is shown that both the amount of adsorbent used and the time after sub-culture at which it is added to the system are critical. The value of such a method for product recovery from immobilised cells is discussed.


Planta | 1990

Factors regulating tropane-alkaloid production in a transformed root culture of a Datura candida × D. aurea hybrid.

Richard J. Robins; Adrian J. Parr; J. Payne; Nicholas J. Walton; Michael J. C. Rhodes

Using in combination an analysis of (i) the levels of enzyme activities present, (ii) the pool sizes of metabolic intermediates and end products and (iii) the effects of feeding metabolic intermediates, the limitations ℴ flux into tropane alkaloids in a Datura root culture have been examined. This culture, produced by transforming a Datura candida × D. aurea hybrid with Agrobacterium rhizogenes, is found to be highly competent in the biosynthesis of both hyoscyamine and scopolamine as well as a wide range of other hygrine-derived alkaloids. It has been found that, of six enzymes which are involved in this pathway, the two initial activities, ornithine decarboxylase (EC 4.1.1.17) and arginine decarboxylase (EC 4.1.1.19), are present at potentially flux-limiting levels, in contrast to those other enzymes assayed which act further down the pathway. An additional limitation to flux, involving the supply of activated acids for condensation with tropine to form the identified tropoyl and tigloyl derivatives, is also indicated from the observed effect of feeding free acids. The relative contribution to flux limitation caused by these two interacting phenomena is inferred from an analysis of the changing relative levels of metabolic intermediates and end products as cultures mature.


Plant Cell Reports | 1991

Abiotic factors elicit sesquiterpenoid phytoalexin production but not alkaloid production in transformed root cultures of Datura stramonium

Judith M. Furze; Michael J. C. Rhodes; Adrian J. Parr; Richard J. Robins; Ian M. Withehead; David R. Threlfall

The treatment of root cultures of Datura stramonium with copper and cadmium salts at external concentrations of approximately 1mM has been found to induce the rapid accumulation of high levels of sesquiterpenoid defensive compounds, notably lubimin and 3-hydroxylubimin. These compounds were undetectable in unelicited cultures. No net change was seen in the alkaloid content of the system following treatment with Cu2+ or Cd2+, the tropane alkaloid titre apparently being insensitive to elicitation. However, a considerable rapid and, in some instances, reversible release of alkaloid was observed. This resulted in the appearance of up to 50–75% of the total alkaloid in the medium after 40–60 h. Subsequently, in cultures treated with Cu2+ ions, though not in cultures treated with Cd2+ ions, this alkaloid was re-absorbed. These observations show how, in a single system, different groups of secondary products can show distinct differences in their responses to potential elicitors.


Plant Cell Reports | 1984

Intracellular distribution of phosphate in cultured Humulus lupulus cells growing at elevated exogenous phosphate concentrations

Richard J. Robins; R. G. Ratcliffe

The distribution of inorganic phosphate (Pi) between the cytoplasm and the vacuole of Humulus lupulus L. cells grown in suspension culture at different exogenous Pi levels was examined by 31-P nuclear magnetic resonance. In growing cells excess Pi accumulated in the vacuoles and the inhibitory effect of high exogenous Pi was not associated with a change in the cytoplasmic Pi level or with a change in the cytoplasmic pH.

Collaboration


Dive into the Richard J. Robins's collaboration.

Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar

David M. Evans

University of East Anglia

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Researchain Logo
Decentralizing Knowledge