We need carrier proteins for steroid hormones because they help in the transportation from the cell they were released from to their target cell.
let me know if you have any further questions
:)
Answer:
All options are correct
Explanation:
Fossils are the remains of organisms (animals and plants) preserved in a rock. Scientists (geologists & palaebiologists) have used fossils to study the diversity of organisms in the past. This is based on their preserved morphological features. For example, several species of foraminifera has been identified in the rocks. Among them, some species are present today whereas others have become extinct.
Similarly, fossils are the indicators of past climate (e.g. temperature) as well. This means, if a specific species can survive at a particular temperature, its presence suggest that particular environment. For example, corals survive in tropical waters at specific depth and sunlight. So, if we find corals fossils, the cliamte of that particular age would be roughly the similar.
In the end, fossils can also provide evidence of orogeny (mountain building) process. These are typically plants fossils which cannot move and their remains are preserved in the folding rocks.
Microorganisms can be divided into two groups:
1. Archea
• Archea are prokaryotic unicellular organisms without cell nucleus or other membrane bound-organelles.
• Their membrane is built from ether lipids, which differs them from bacteria’s cell membrane.
•
2. Bacteria
• Bacteria are also unicellular prokaryotic organisms.
• Bacterial cell membranes are made from phosphoglycerides with ester bonds. Bacterial genome is in a form of circular chromosome.
• They reproduce by binary fission or by budding.
Besides, prokaryotes (Archea and Bacteria) a large number of eukaryotes are also microorganisms. Unicellular eukaryotes contain organelles such as the cell nucleus, the Golgi apparatus and mitochondria. Usually, they reproduce asexually by mitosis. An example of eukaryotic microorganism is Protist.
Explanation:
Almost all eukaryotic proteins are subject to post-translational modifications during mitosis and cell cycle, and in particular, reversible phosphorylation being a key event. The recent use of high-throughput experimental analyses has revealed that more than 70% of all eukaryotic proteins are regulated by phosphorylation; however, the mechanism of dephosphorylation, counteracting phosphorylation, is relatively unknown. Recent discoveries have shown that many of the protein phosphatases are involved in the temporal and spatial control of mitotic events, such as mitotic entry, mitotic spindle assembly, chromosome architecture changes and cohesion, and mitotic exit. This implies that certain phosphatases are tightly regulated for timely dephosphorylation of key mitotic phosphoproteins and are essential for the control of various mitotic processes. This review describes the physiological and pathological roles of mitotic phosphatases, as well as the versatile role of various protein phosphatases in several mitotic events.
Eat It because it tastes really really good
