Answer:
The correct answer is -transfer fixed carbon dioxide to cells in which the Calvin cycle occurs
Explanation:
In C4 plants the light reaction and Calvin cycle occurs in two different cell that are mesophyll cell and bundle sheath cells. First, the CO₂ is fixed into 4- carbon oxaloacetate by an enzyme PEP carboxylase.
Then this oxaloacetate is converted into a simpler form called malate. Malate molecule then enters into bundle sheet cell and there it releases one molecule of CO₂. This CO₂ enters the Calvin cycle which results in the sugar formation with the help of enzyme rubisco.
Therefore by releasing of CO₂ molecule by malate in bundle sheet cells, it transfer fixed carbon for the Calvin cycle to occur.
Answer:
<h3>Offspring receive chromosomes from their parents, each chromosome contains alleles, each allele contains genes which determine the appearance of an organism</h3>
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edlyn moreno
SBP is a serious complication in patients with cirrhosis with high mortality rates (20–40%).
Patients at risk of developing SBP can be categorized in three groups firstly patients with active variceal bleeding patients with ascitic fluid protein <10 g/dl secondly those with a prior episode of SBP.
The most common bacteria causing SBP are gram-negative Escherichia coli and Klebsiella pneumoniae and gram-positive Streptococcus pneumoniae usually only a single organism is involved. Spontaneous bacterial peritonitis (SBP), an infection of ascitic fluid without a definitive intra-abdominal source that can be surgically treated is a common complication in patients with cirrhosis and ascites. Spontaneous bacterial peritonitis (SBP),is treated with a 10 to 14 day course of antibiotics .
To learn more about Spontaneous bacterial peritonitis (SBP) , here
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Answer:
no 1 ok
Explanation:
because it controls the raye pf breathing so
Answer:
A few obstacles would make it tough to accomplish this objective. In the first place, the polypeptide backbone is characteristically polar. Hardly any proteins would be dissolvable in a non-polar hydrocarbon. Moreover, to keep up the dissolvability of this protein, most of its amino acids would need to contain hydrophobic or non-polar R groups.
Then again, its charged or polar R groups would need to connect with one another or be covered in the core of the protein away from the hydrocarbon solvent. This would put noteworthy requirements on both the idea of the R groups and the structure of the protein that could take part in substrate recognition or catalysis. By and large, this is certainly not a reasonable objective.
