The codons that encodes amino acid serine are as follows:
- TCT,
- TCC,
- TCA,
- TCG,
- AGT,
- AGC
1. 186.6 g (C)
2. 24
3. Synthesis
4. Endothermic
5. Rate
6. Accelerate
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Answer: Many pathogenic fungi are parasitic in humans and are known to cause diseases of humans and other animals. In humans, parasitic fungi most commonly enter the body through a wound in the epidermis (skin). Such wounds may be insect punctures or accidentally inflicted scratches, cuts, or bruises. One example of a fungus that causes disease in humans is Claviceps purpurea, the cause of ergotism (also known as St. Anthony’s fire), a disease that was prevalent in northern Europe in the Middle Ages, particularly in regions of high rye-bread consumption. The wind carries the fungal spores of ergot to the flowers of the rye, where the spores germinate, infect and destroy the ovaries of the plant, and replace them with masses of microscopic threads cemented together into a hard fungal structure shaped like a rye kernel but considerably larger and darker. This structure, called an ergot, contains a number of poisonous organic compounds called alkaloids. A mature head of rye may carry several ergots in addition to noninfected kernels. When the grain is harvested, much of the ergot falls to the ground, but some remains on the plants and is mixed with the grain. Although modern grain-cleaning and milling methods have practically eliminated the disease, the contaminated flour may end up in bread and other food products if the ergot is not removed before milling. In addition, the ergot that falls to the ground may be consumed by cattle turned out to graze in rye fields after harvest. Cattle that consume enough ergot may suffer abortion of fetuses or death. In the spring, when the rye is in bloom, the ergot remaining on the ground produces tiny, black, mushroom-shaped bodies that expel large numbers of spores, thus starting a new series of infections.
The oxygen atoms i believe is the answer
The right answer is A) Trisomy
Aberrant karyotypes containing an abnormal number of chromosomes are known in the human species. The best-known (and most common) chromosomal abnormality is trisomy 21, which is responsible for Down syndrome (mongolism). There are others such as Turner syndrome (woman with a single X chromosome) or Klinefelter syndrome (man XXY).
These abnormalities originate from the non-disjunction of the chromosomes of a pair of homologues during metaphase I of meiosis. At the end of division I, a daughter cell contains the two chromosomes of the pair considered and the other cell does not contain a chromosome of this pair. A similar result can be obtained during a bad distribution of chromatids during anaphase II.
After fertilization from a gamete of this type, a trisomy or a monosomy is obtained.