# Microscopes and Bacteria

## Cell Differentiation

As an organism develops, cells differentiate to form different types of cells.

• Most types of animal cell differentiate at an early stage.
• Many types of plant cells retain the ability to differentiate throughout life.
• In mature animals, cell division is mainly restricted to repair and replacement.

As a cell differentiates it acquires different sub-cellular structures to enable it to carry out a__ certain function__. It has become a specialised cell.

## Scale and Size

A scale bar may be used in order to find the magnification of the image:

In order to work out the magnification of the image:

1. Measure the scale bar image in millimeters (the line below 100nm)
2. Convert the number that you have measured into nm (so that you are now working with the same units)
3. Magnification = measured length / the number written (they should both have the same units)

Remember to convert between the different units! You also need to know how to write numbers in the standard form.

E.g. 7000 is written as 7 x 103

``````   0.000007 is written as 7 x 10__-6__
``````

## Microscopes

Changes in microscope technology, including electron microscopy, have enabled us to see cell structures and organelles with more clarity and detail than in the past and increased our understanding of the role of sub-cellular structures. However, it does not allow us to view living cells.

Light microscopes are used to study living cells. It provides low magnification and resolution, but it is usually sufficient for regular use.

Using the following formula, you can calculate the magnification of an image.

Don’t forget to convert between different units of measurement when calculating the magnification - the unit of measurements must always be the same

E.g. if you have to convert 100 micrometres to nanometers, you have to multiply 100 by 1000.

Therefore 100 micrometres = 100,000 nanometres

## Binary Fission

Bacteria multiply by simple cell division (binary fission) as often as once every 20 minutes if they have enough nutrients and a suitable temperature.

Bacteria can be grown in a nutrient broth solution (allows a liquid or gel to provide nutrients that a bacteria needs in order to grow) or as colonies on an agar gel plate.

Uncontaminated cultures (otherwise other contaminating bacteria will try to compete for nutrients) of microorganisms are required for investigating the action of disinfectants and antibiotics.

﻿

## Aseptic Techniques

Aseptic techniques must be used when culturing microorganisms in the laboratory so that there isn’t any bacteria that is trying to compete for nutrients in the petri dish. Harmful pathogens can also damage the results that are being collected.

An autoclave must be used to prepare sterile growth medium and petri dishes. Sterile inoculating loops must be used to transfer microorganisms. The inoculating loop is sterilised when it is heated to red hot under a bunsen burner flame before and after use. Petri dishes and culture vials must also be covered.

## Colonies

The cross-sectional areas of colonies or clear areas around colonies can be calculated using the formula:

This can be used so that you can see how effective a specific antibiotic or antiseptic is.

You need to look at the growth inhibition zone (the area outside surrounding the antimicrobial disk. Based on the image below, it is the gray area. To find the radius, measure the diameter, then divide it by 2.

= 3.14

What is binary fission?