Answer:
A differential medium
Explanation:
Bacteria require nutrients for growth, and in order to culture (grow) them and study their characteristics, different types of media are used.
A selective media is used to grow a particular group of organism while suppressing another. So a selective media usually has an inhibitory agent, which will inhibit the growth of the undesired group. An antibiotic can be added to a medium to make it selective.
A general purpose medium as the name implies can be used to grow any group of bacteria. It has no inhibitory agent and indicator that differentiates between organisms. An example of general purpose media is nutrient agar
.
A non-synthetic media is made from natural ingredients.
A differential media differentiates between groups of organisms. Example of differential media is MacConkey agar and Mannitol Salt agar. On MacConkey agar, lactose fermenting bacteria turn pink while non-lactose fermenting bacteria are colorless.
On Mannitol Salt agar, mannitol fermenting bacteria turn yellow while non-mannitol fermenting bacteria are colorless. Mannitol Salt agar is also a selective medium. It has a high salt concentration which inhibits certain organisms.
Because these non native species can cause competition for the same food source as the native species thus making it harder for the native species to survive. Also the non native species could see the native species as food causing them to die out. As well as introducing new diseases that these native species don’t know how to defend themselves from
<span>Some mutations don't have any noticeable effect on the phenotype of an organism. This can happen in many situations: perhaps the mutation occurs in a stretch of DNA with no function, or perhaps the mutation occurs in a protein-coding region, but ends up not affecting the amino acid sequence of the protein.</span>
Answer:
Molecular genetic approaches to the study of plant metabolism can be traced back to the isolation of the first cDNA encoding a plant enzyme (Bedbrook et al., 1980), the use of the Agrobacterium Ti plasmid to introduce foreign DNA into plant cells (Hernalsteens et al., 1980) and the establishment of routine plant transformation systems (Bevan, 1984; Horsch et al., 1985). It became possible to express foreign genes in plants and potentially to overexpress plant genes using cDNAs linked to strong promoters, with the aim of modifying metabolism. However, the discovery of the antisense phenomenon of plant gene silencing (van der Krol et al., 1988; Smith et al., 1988), and subsequently co‐suppression (Napoli et al., 1990; van der Krol et al., 1990), provided the most powerful and widely‐used methods for investigating the roles of specific enzymes in metabolism and plant growth. The antisense or co‐supression of gene expression, collectively known as post‐transcriptional gene silencing (PTGS), has been particularly versatile and powerful in studies of plant metabolism. With such molecular tools in place, plant metabolism became accessible to investigation and manipulation through genetic modification and dramatic progress was made in subsequent years (Stitt and Sonnewald, 1995; Herbers and Sonnewald, 1996), particularly in studies of solanaceous species (Frommer and Sonnewald, 1995).
Plates collide causing rock to push upward together
