Selection is the genetic factor that determines the primary sources of active ingredients, in particular cultivated plants and biotechnologies.
In the biotechnology field, selection is applied to isolate those cells which, when transferred to an in vivo culture, serve to improve biotechnological productivity in terms of production of active but also bio-transformative ingredients.
Selection can be considered as the most exploited genetic element in the pharmacognostic field, to improve the quality of drugs; it is an endogenous factor, but which is independent of what is the "operation of" man, which fundamentally also belongs to the "hybridization, and to a lesser extent polyploidy.
Some examples of genetic factors used by biotechnologies, intended as resources of active principles or bio-transformative elements, are selection and induced gene mutation; these are two biotechnological elements that are reflected, for example, in the production of an active ingredient of particular interest such as penicillin. We could also speak of hormonal molecules such as insulin, in this case of human derivation.How, however, to obtain these types of complex products, from organisms cultivated in vitro (organisms in general, not only plant cells, but also fungi and bacteria)? To determine the importance of genetic factors in biotechnologies, we can consider that these, as a source of active principles, use not only plant cells but also bacteria and cells of eukaryotic organisms.
Biotechnologies are nature transported to the laboratory, and represent the ability of man to manipulate this nature at will, as he did with GMOs (Genetically Modified Organisms). A genetically modified organism is an organism that does not belong to nature, but rather to biotechnology.
The use of bacteria and microorganisms to obtain active ingredients represents a particularly useful biotechnological strategy to obtain them with a greater yield and in the shortest possible time (active ingredients that in nature belong to that organism, as in the case of a mold which is part of the type Penicillium for penicillin, or active principles that in nature do not belong to that microorganism, but which become so in the biotechnological field because a gene sequence is inserted in its DNA that codes for the production of the enzymes involved in the biogenesis of that active ingredient).
If a gene sequence linked to the production of a certain active ingredient is identified, that fragment of DNA can be taken and inserted, for example, into a bacterium, which has an ontogenetic cycle enormously faster than that of a eukaryotic organism. A bacterial culture, in fact, reaches its peak of growth within 6/8 hours; this means that in that time the organisms present inside the culture medium have consumed most of the nutritional elements and consolidated their biological cycle. , undergoing various cell divisions, thanks to a much faster metabolism than that of a plant cell (which reaches the stationary phase after several days, sometimes even 20/30 days).
Productivity, therefore, in terms of quality and quantity, is extremely favored by a microbial culture. The transition from theory to practice lies in the ability or inability of the operator to identify, or not, particular genomic sequences, and then transfer them to bacteria or other microorganisms. The problem, in particular, lies in the difficulty of encoding the genetic code of a plant source and transfer it to an organism with a much faster ontogenetic cycle. However, although this is characterized as the main or most important goal of certain biotech industries in the pharmaceutical sector, many companies have developed into "deepening and improving crops in vitro of bacteria, fungi or plant cells, in order to obtain the maximum productivity by exploiting genetic factors, first of all the selection. If a strain of Penicillium is cultivated in vitro with the aim of optimizing the production of penicillin, for example , the individuals who produce the most will be selected.
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