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Total Viable Count of bacteria gives a quantitative idea about how much is in a sample. The calculation represents the number of colony forming units (cfu) per g ( or per ml).

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Does a spectrophotometer measure total cell count or viable cell count?

A spectrophotometer measures the optical density of a sample, which can be used to estimate total cell count in a sample. It does not distinguish between viable and non-viable cells, as both contribute to the absorption of light. To determine viable cell count, additional methods such as colony-forming unit assays or flow cytometry are typically used.


What is affect of spores on tpc count?

Spores do not contribute to the total plate count (TPC) as they do not metabolize on standard culture media used for TPC determination. Only viable bacteria that can grow and form colonies will affect the TPC count. Spores may appear on plates as the result of sporulation by certain bacteria, but they are not included in the TPC calculation.


What is total plate count in water?

Total Plate Count (TPC) in water is a measure of the total number of viable bacteria in a given sample of water. It is used as an indicator of overall water quality and can help determine if the water is safe for consumption or other purposes. High TPC levels may indicate contamination and potential health risks.


What is most viable count?

"Most viable count" is a term used in microbiology to refer to the number of viable microorganisms in a sample. It is often determined through techniques like colony counting on agar plates or turbidity measurements. This count is important for assessing the presence and concentration of microorganisms in a sample.


There are other techniques for counting bacteria such as a direct microscopic count and turbidity Why is the standard plate count preferrend for food?

The standard plate count method is preferred for counting bacteria in food because it provides a simple and reliable way to determine the number of viable bacteria present. It allows for the cultivation of various types of bacteria which may be present in the sample, providing a more accurate representation of the bacterial population. Additionally, the standard plate count method is well-established, widely accepted, and can be easily standardized for regulatory purposes in the food industry.

Related Questions

What does TVC stand for in meat?

TVC stands for Total Viable Count and is usually referred to when counting bacteria in meat.


Does the number of bacteria recorded by the standard plate count method accurately reflect the total bacterial count from the sample?

No. The standard plate count method is an indirect measurement of cell density of only viable bacterial cells. Optical density counting measure entire bacterial sample, the living as well as the dead bacterial cells.


Name the units used for measuring micro-organisms.?

Total Viable Count,(TVC) or Total bacterial Count,(TBC)


Does a spectrophotometer measure total cell count or viable cell count?

A spectrophotometer measures the optical density of a sample, which can be used to estimate total cell count in a sample. It does not distinguish between viable and non-viable cells, as both contribute to the absorption of light. To determine viable cell count, additional methods such as colony-forming unit assays or flow cytometry are typically used.


What is affect of spores on tpc count?

Spores do not contribute to the total plate count (TPC) as they do not metabolize on standard culture media used for TPC determination. Only viable bacteria that can grow and form colonies will affect the TPC count. Spores may appear on plates as the result of sporulation by certain bacteria, but they are not included in the TPC calculation.


What is total plate count in water?

Total Plate Count (TPC) in water is a measure of the total number of viable bacteria in a given sample of water. It is used as an indicator of overall water quality and can help determine if the water is safe for consumption or other purposes. High TPC levels may indicate contamination and potential health risks.


How do you measure bacteria in a petri dish?

When bacteria is grown in an Agar plate, one quantitative method to measure growth is using a counting chamber. Another method is using viable plate counts.


Why is turbidity not an accuarte measure of viable bacteria in a culture?

Turbidity measures the cloudiness of a culture, which can be influenced by various factors besides viable bacteria, such as debris or particles in the solution. Viable bacteria may also form clusters or biofilms, which can affect turbidity readings. To accurately measure viable bacteria, other methods such as colony counting or molecular techniques are more appropriate.


What is most viable count?

"Most viable count" is a term used in microbiology to refer to the number of viable microorganisms in a sample. It is often determined through techniques like colony counting on agar plates or turbidity measurements. This count is important for assessing the presence and concentration of microorganisms in a sample.


There are other techniques for counting bacteria such as a direct microscopic count and turbidity Why is the standard plate count preferrend for food?

The standard plate count method is preferred for counting bacteria in food because it provides a simple and reliable way to determine the number of viable bacteria present. It allows for the cultivation of various types of bacteria which may be present in the sample, providing a more accurate representation of the bacterial population. Additionally, the standard plate count method is well-established, widely accepted, and can be easily standardized for regulatory purposes in the food industry.


What are the bacteriological parameters in water by USPH standards?

1. Coliform cells. 2.Total bacteria count


Why direct microscopy and plate count give not a same counts?

Direct microscopy counts viable and non-viable cells, whereas plate count only counts viable cells that are able to grow and form colonies on agar plates. Additionally, plate count may underestimate the total number of viable cells due to factors like the inability of certain cell types to grow under specific conditions or the formation of aggregated cells that do not separate easily on the agar plate.