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Microbiological Testing

of Foods, Beverages, Drinking Water


and Pharmaceuticals
Introduction
The consumer’s steadily growing requirements for the quality and the longer shelf life
of foods and beverages must be met by the manu­facturer. Quality assurance can’t be
limited to inspection of the final product alone, such as a bottled beverage or a prepared
food product. Instead, continuous inspection of incom­ing raw materials and in-process
quality control tests must be performed throughout production. Microbiological and
aseptic testing play a significant role in such quality assurance.

In the soft drink industry the microbio­logical and hygienic quality including the
biological stability of the products are important criteria for their assessment. The reason:
just a few microbes are often all it takes to spoil large quantities of a beverage.

Although the explosive technological development has reduced the risk of contamination
by spoiling microbes, the issue of shelf life has taken on new dimensions as a result
of the enormous production output possibilities of today. Quality control of bottling and
filling, in terms of chemical and, above all, biological stability, must be adapted to this
development by state-of-the-art test methods.

The requirements for a practical micro­­­bio­logical test method are that it permits
quantitative and reproducible detection of trace contamination and that it can
be performed efficiently and economically under routine conditions.
These requirements are fulfilled optimally by the membrane filter method.

The principle of this method is based on the concentration of microorganisms from


relatively large samples on the surface of the membrane filter, and on culturing
these microbes on a nutrient pad or an agar culture medium.
Contents
4 The Membrane Filter Method 21 Membrane Filters for Use with
Microsart® e.motion Dispenser
6 Nutrient Pad Sets
22 Typical Application Examples
6 User Benefits
7 How to Use Nutrient Pad Sets 23 Growth comparison

8 General Directions 24 Accessories

9 Description and Typical Growth 28 Technical Data and Application Guide


Evaluation Results Nutrient Pad Sets
9 1. Total Colony Count
32 Test Strains
11 2. E. coli and Coliforms,
Enterobacteria 34 Reference Guide
13 3. Faecal Bacteria
14 4. Non-faecal, Pathogenic Bacteria
14 5. Yeasts and Molds
16 6. Product-spoiling Microorganisms

19 Troubleshooting Guide

19 Membrane Filters for Use on


Agar Plates or on Aborbent Pads

3
The Membrane Filter Method
Description The Advantages: The Culture Media
The Membrane Filter Method Microorganisms can be detected by
– Proofen accuracy
A membrane filter of the appropriate pore different methods.
Compared with the direct method,
size is placed in a filter holder, and the
considerably larger sample volumes
sample is filtered. In this process micro­ Methods involving culturing techniques
can be tested. This concentration effect
organisms in the test sample are retained and the microscope are used to detect
increases the accuracy of microbial
on the filter surface by the screening microbes, whereas biochemical and sero-
detection.
action of the membrane filter. logical techniques are commonly applied
– Quantitative results to differentiate among such organisms.
Growth inhibitors can be removed by The visible colonies can be related
flushing the membrane with sterile NaCl directly to the sample volume. For detecting microorganisms in cultures,
solution after filtration. Afterwards, the liquid and solid culture media are employed.
– Documentation
membrane filter is placed on a culture Microorganisms are concentrated by
The membrane filter with colony growth
medium and incubated. growth in or on these culture media.
can be filed as a permanent record of
the test.
For the Monitor MF-Methode the monitor Quantitative detection is only possible
is ready to use due to a pre-asembled with solid culture media because the
No Inhibitors
membrane and pad inside. individually developing colonies can be
Inhibitors, such as essential oils or disinfec-
evaluated and counted on the surface.
tants, can be flushed from the membrane
The nutrient media is added from the top
filter after filtration.
and sucked into the pad by a short vacuum The following culture media can be used
(< 1 sec.) After removal of the funnel the for microbiological testing:
GMP Quality
lid and the base fit to a petri dish.
Sartorius Stedim Biotech Membrane Filters – Nutrient Pad Sets
are manufactured under GMP conditions, Nutrient Pad Sets definitely optimize
Nutrients and metabolites are exchanged
ensuring consistently quality and high the membrane filter method.
through the pore system of the membrane
reproducibility from batch to batch and They standardize microbiological
filter. Colonies, which have developed
within each batch. test procedures, making them much
on the membrane filter surface during
more efficient.
incubation, are counted and related to the
The simplify laboratory work.
sample volume.
They help to save time and money.

– Absorbent pads to be wetted with


culture media.
– Culture media with agar or gelatin
as the solidifying agent.

The nutrient Pad Sets are described on the


following pages and certainly offer the
most convenient way to use the membrane
filter method.

4
Direct Method Membrane Filter Method
The test sample is pipetted into The test sample is filtered through
a petri dish … a membrane filter

Standard MF method Monitor MF method


The membrane filter is rinsed
and then placed on a culture
medium – a, b, or c –
… then mixed with the culture and incubated.
medium and incubated

The nutrient media is given from


the top after filtration. After a short
vacuum (<1 sec.), the monitor is
closed with the plug at the bottom.
Remove the funnel, fit lid and base
to a petri dish.

a) on a nutrient b) on an c) on an agar


pad wetted absorbent plate
with sterile pad wetted
water with liquid
culture For further information on
medium Sartorius Stedim Biotech
Biosart 100 Monitors, please
refer to the publications
SM-1013-e

5
Nutrient Pad Sets
Sartorius Stedim Biotech Nutrient Pad The membrane filters tailored to meet the
Sets have been used successfully in the special requirements of microbial detection
membrane filter method for over 20 years. are available with 47 mm or 50 mm
Practical and easy to handle, they reduce diameters.
labor and simplify many microbiological
testing procedures. Nutrient pad sets (NPS) are continuously
enhanced as part of our development pro-
Nutrient pads are sterile, dehydrated gram to adapt our products to changing
culture media. Once they are moistened with application requirements. Besides the
3.0–3.5 ml of sterile and demineralized new NPS types, we have also updated our
(or distilled) water they are ready to use packaging design. The standard NPS box
immediately. contains 100 sterile nutrient pads, each of
which is individually inserted in a petri
The level of moisture is optimal when an dish and sterilized. Ten each of these petri
excess ring of water surrounding the pad dishes are sealed in an aluminum bag.
is visible. This special packaging in bags protects
the sensitive formula constituents of the
All Nutrient Pad Set types are supplied nutrient pads during transport and storage
with the appropriate membrane from fluctuations in humidity and
filters, which are also presterilized and temperature. As a result, it guarantees
individually packaged or dispenser-ready the high quality of our NPS throughout
packaged on a band for the use with their entire shelf life of up to 24 months.
the Microsart® e.motion dispenser.

User Benefits
Economical
Eliminates time-consuming and labor-intensive – After wetting with 3.5 ml
preparation of culture media destilled water NPS are ready
(sterilization and cleaning, among others). to use: NPS and go
Simple to Use
Nutrient Pad Sets can also be used in laboratories – Everyone can use NPS
which do not have extensive microbiological
equipment. Sterile water for moistening the pads can
be added easily with a Sartorius Stedim Biotech
Dosing Syringe and an attached Syringe Filter Holder
(0.2 µm) or with an ampoule with sterile water.
Consistently Quality
During manufacture, each type of Nutrient – NPS are validated. In com­
Pad Set is compared with the corresponding parison to agar which is done
agar medium with respect to their growth- within different deviations
promoting properties. This QA procedure ensures of amount and height NPS
consistent quality and reproducible results. always give constant results
Trouble-free Storage
Nutrient Pad Sets have a shelf life of – No waste or overproduction
up to 24 months at room temperature. of prepared agar media
Highly Versatile
Nutrient Pad Sets can be modified by additives in the – A
 dvanced system
solution used to wet them; for example, Wort or
Orange Serum Nutrient Pads when wetted with 5 – 8%
ethanol promote the growth of acetic-acid bacteria

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How to Use Nutrient Pad Sets

It’s so easy to use Nutrient Pad Sets: NPS and go

1   Before starting with the tests remove everything 9


The forceps should always 15
 Place the filter on the
that is not essentially needed for this work. be stored in a small glass Nutrient Pad, avoid to
with alcohol. entrap air bubbles under
2   Carefully
 clean and disinfect your working area. the filter.
Take it out of it and flame it.
3 For simple microbiological tests a laminar flow
  box is not needed. When used unprofessionally, a Let it cool off for a few
Open the lid of the Petri
dish only slightly to avoid
laminar flow box increases the risk of secondary seconds before use. airborne contamination.
contamination instead of protecting from it. A
good protection against airborne contamination,
however, is to work close to the flame of a Bunsen
burner.Instruments like forceps should be placed Let the Microsart® e.motion Place the Petri dish into the
into a glass with alcohol. 10 Dispenser release the mem-
16 incubator, lid above.
brane filter automatically by
approaching tweezers or by Incubate strictly according
4
Label the needed amount
press button. to the recommendations.
of Nutrient Pads.
Alternatively you peel back Evaluate immediately after
the transparent plastic layer the end of the
of the membrane filter pack- incubation time.
aging manually.
Use tweezers to remove the
content out of the packaging.

Wet the Nutrient Pad with  The membrane filter is placed


5 3.5 ml of sterile, deionized
11
by the tweezers onto the filter
or distilled water. support of the filter holder.
Use a dosing syringe with a The protective paper or grid
Minisart® or a sterile pipette. should face upwards. If there
is a protective disc make sure
Open the lid of the Petri
to discard it before assem-
dish only slightly to avoid
bling the funnel or the top
airborne contamination.
part of the filter holder.

6
Open the vacuum 12
 Place the funnel on the
valve. filter support and close it
(6 o’clock1) with the clamp.
Carefully flame the
filter support for For long time filtration
~10 sec. cover the funnel with
the lid.
Close the vacuum
valve again.
(9 o’clock2)

7
Take the funnel at both 
13 Open the valve and
sides of the clamp and filter the sample. 3 o’clock – After the Filtration Run
flame it from its lower side (6 o’clock1) The residual vacuum between the
for ~10 sec. Rinse with a few mls pump and valve is released via the
of sterile water to venting filter.
Then place it on the filter remove all product
support. residues or inhibitors 12 o’clock – For Autoclaving
that might be con- For reliable sterilization, the steam flows
tained in the sample. freely through all openings.
Close the valve 1)
 6 o’clock – For Filtration
again.
8
Open the vacuum
(9 o’clock2).
The tap is open. The full vacuum is
valve again. effective at the filter support|membrane
(6 o’clock1) filter. The venting filter is “off-line”.
Flame the inside of
the funnel. 14
 Remove the funnel and take 2)
 9 o’clock – After Filtration
the filter with the sterile The tap is closed. The vacuum between
Close the valve forceps. the valve and membrane filter is released
again. under sterile conditions. Secondary
(9 o’clock2) contamination of the bottom of the
filter is ruled out entirely.
To cool it off faster,
rinse with a few ml
of sterile water.

7
General Directions
General Procedure Do not touch bacterial matter with
To obtain reliable results for microbio­ your hands.
logical tests, it is necessary to work under
conditions that rule out contamination by Before and after use, inoculating loops and
microorganisms which distort such results. wires must be sterilized by flaming until
they glow red-hot.
That is why it is recommended to work near
the flame of a Bunsen burner in a room All laboratory equipment which has come
protected from drafts. Before beginning in contact with bacteria must be sterilized.
with the actual procedure, spraying or
washing down the working area with a dis- To protect people and animals from
infectant is mandatory (e.g., 70% alcohol). con­tagious diseases or poisoning, living
cultures have to be destroyed before
Before use, filter holders, tweezers and cleansing or disposing of the containers.
scissors should be sterilized by one of One method is to coat them thoroughly
the standard methods, such as flaming with disinfectants or to autoclave them
for routine tests. in suitable containers.

How to Handle Microorganisms Sartorius Stedim Biotech Nutrient Pads are


Microorganism cultures must always be participating regularly at official inter-lab-
handled as carefully as if they contained oratory tests for the microbiological inves-
pathogens. tigation of drinking water according to the
New European Drinking Water Guideline.
Working with microorganisms is not This certificate of the “Niedersächsischen
dangerous if the following safety rules Landesgesund­heits­amt“ in Aurich (public
are observed: health agency, Lower Saxony) quote
a reference for the passed tests with good
Wash your hands thoroughly before and success.
after working in a laboratory.

Do not eat or drink in a laboratory.

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Description and Typical Growth Evaluation Results
1. Total Colony Count
Caso NPS R2A NPS Standard TTC (I mod.) NPS
Type 14063 Type 14084 Type 14055

Soybean-Casein Digest medium for isolating Low nutrient medium for the enumeration Meat extract-peptone medium for deter­
microorganisms and for determining the of heterophilic organisms in treated mining the total CfU count based on
total CfU count. Dehydrated culture potable water and highly purified water. the “APHA (water)” and modified by the
medium for cultivating microorganisms in Growth medium for microorganisms addition of TTC.
pharmaceuticals, cosmetics, raw materials, which have adapted to the particular living Dehydrated culture medium for cultivating
water (general quality), waste water, foods conditions of water low in nutrients. microorganisms in raw materials, water
and other products. Dehydrated culture medium for cultivating (general quality), waste water, beverages,
microorganisms in water for pharmaceuti- beer, foods and other products.
References: cal purpose, water (general quality), waste
APHA (dairy), APHA (food), APHA (water), water and other products. References:
AOAC, DAB, EG 98/83, EP, FDA, IDF, ISO 7704, APHA (water), ISO 7704, VLB
ISO 8199, ISO 9308-1 [1990], ISO 9308-1 References:
[2001], USDA, USP APHA (water), EP, ISO 7704 Incubation Conditions:
< 5 days at 30–35°C
Incubation Conditions: Incubation Conditions:
Bacteria: < 3 days at 30–35°C > 5 days at 30–35°C Evaluation and Typical Results:
Yeasts and molds: < 5 days at 30–35°C Predominantly bacteria grow on this
Evaluation and Typical Results: medium. The majority of their colonies
Evaluation and Typical Results: Predominantly bacteria grow on this medi- are stained red by TTC reduction.
Predominantly bacteria of different sizes, um. Their colonies are of different size and
shapes and colors. Remarks: Depending on the color, most of them are white or colorless.
microbes to be detected, this medium can be Remarks: Stressed and chlorine-tolerant
converted into a selective one. When 10% bacteria are stimulated by this medium
serum is added to the wetting liquid a number in combination with lower incubation
of fastidious pathogenic bacteria like the gen- temperatures and longer incubation time.
era Pneumococcus, Neisseria, Streptococcus,
Corynebacterium, Erysipelothrix and Brucella
are able to grow on the medium.

Staphylococcus aureus Escherichia coli Bacillus subtilis

Mixed culture from process water Mixed culture from water Mixed culture from well water

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1. Total Colony Count

Standard NPS TGE NPS Yeast Extract NPS


Type 14064 Type 14076 Type 14090

Meat extract-peptone medium for deter­ Tryptone Glucose Extract medium for iso­ For the detection of the total count of
mining the total CfU count; based on the lating micro­organisms and for determining aerobic heterotrophic bacteria. Dehydrated
“APHA (water)”. the total CfU count. Dehydrated culture culture medium for cultivating micro­
Dehydrated culture medium for cultivating medium for cultivating microorganisms organisms in water (general quality) and
microorganisms in raw materials, water in raw materials, water (general quality), other products.
(general quality), waste water, beverages, waste water, beverages, soft drinks,
beer, foods and other products. concentrates, foods and other products. References:
EG 98/83, HMSO, ISO 6222, ISO 7704,
References: References: ISO 8199
APHA (water), ISO 7704, VLB APHA (dairy), APHA (food), APHA (water),
API, ISO 7704 Incubation Conditions:
Incubation Conditions: 44 ±4 hours at 36 ±2°C;
< 5 days at 30–35°C Incubation Conditions: 68 ±4 hours at 22 ±2°C
< 5 days at 30–35°C
Evaluation and Typical Results: Evaluation and Typical Results:
Predominantly bacteria grow on this Evaluation and Typical Results: Predominantly bacteria grow on this
medium. The morphology and color of On this medium predominantly colonies medium. The majority of all colonies
their colonies vary. of bacteria grow that can have different are colorless.
size and colors.

Escherichia coli Escherichia coli Escherichia coli

Mixed culture from drinking water Mixed culture from water Mixed culture from river water

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2. E. Coli and Coliforms, Enterobacteria

CHROMOCULT ® * NPS ECD NPS Endo NPS


Type 14087 Type 14082 Type 14053

For the detection of total coliforms and Selective culture medium for detecting Selective medium for detecting and
Escherichia coli. Dehydrated culture and identifying Escherichia coli. Bile salt enumerating E. coli and coliform bacteria.
medium for cultivating microorganisms inhibits the accompanying flora of microbes Dehydrated culture medium for cultivating
in raw materials, water (general quality), not living in the intestine. Dehydrated microorganisms in raw materials, water
waste water, beverages, foods and culture medium for cultivating micro­ (general quality), natural water, waste
other products. organisms in raw materials, water water, beverages, soft drinks, concentrates,
(general quality), waste water, beverages, fruit juice, sugar, sugar products, foods
References: foods and other products. and other products.
ISO 7704, Journal Food Protection,
ZenHyg (journal of hygiene) References: References:
APHA (water), DIN 10110, EG 98/83, APHA (dairy), APHA (food), APHA (water),
Incubation Conditions: ISO 7704, ISO 8199, ISO 9308-1 [2001], DGHM, ISO 7704, ISO 9308-1 [1990], MNO,
20–28 hours at 36 ±2°C LMBG, USDA USDA

Evaluation and Typical Results: Incubation Conditions: Incubation Conditions:


E. coli develops dark-blue to violet colonies, 16–18 hours at 44 ±2°C 18–24 hours at 36 ±2°C
other coliforms red to pink colonies. Other
gram-negative colonies are colorless, a few Evaluation and Typical Results: Evaluation and Typical Results:
with ß-Glucuronidase activity are light blue Colonies that show light blue fluorescence E. coli form red colonies with a metallic
to turquoise. Remarks: To confirm E. coli under UV light indicate E. coli; confirma- sheen and a red dot at the underside of
give one drop of Kovacs indole reagent on tion with a drop of KOVÁCS indole reagent the membrane. Other coliforms grow as
each dark blue colony. Cherry red color is required, a positive reaction is shown dark to light red colonies without metallic
after a few seconds is a positive reaction. by a cherry color after a few seconds. sheen. Colorless colonies of lactose-
Remarks: This medium can be used for the negative bacteria are not counted.
rapid detection of Escherichia coli based
* Trade mark owner and manufacturer on the ISO 9308-1.
is Merck KGaA

Escherichia coli Escherichia coli Escherichia coli

Mixed culture from water E. coli colonies fluoresence in UV light E. coli and coliforms from river water

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2. E. Coli and Coliforms, Enterobacteria

MacConkey NPS m FC NPS Teepol NPS


Type 14097 Type 14068 Type 14067

For the isolation and differentiation of coli­ For the detection of E. coli and faecal coli­ Lauryl Sulphate medium for the detection
form bacteria and other enterobacteriaceae. form bacteria according to Geldreich et al. of E. coli and faecal coliform bacteria
Dehydrated culture medium for cultivating Dehydrated culture medium for cultivating according to Burman, N.P. (1967).
microorganisms in pharmaceuticals, microorganisms in raw materials, water Dehydrated culture medium for cultivating
cosmetics, raw materials, water (general (general quality), waste water, beverages, microorganisms in water (general quality),
quality), natural water, waste water, foods and other products. waste water, beverages, foods and other
beverages, soft drinks, concentrates, fruit products.
juice, foods and other products. References:
APHA (food), APHA (water), AOAC, EPA, References:
References: FDA, ISO 7704, ISO 9308-1 [1990], USDA AFNOR, APHA (water), BS, FDA, ISO 7704,
APHA (dairy), APHA (food), APHA (water), ISO 9308-1 [1990], USDA
AOAC, DAB, DIN 38411, DGHM, EP, ISO Incubation Conditions:
7704, LMBG, MNO, USDA, USP 18–24 hours at 36 ±2°C Incubation Conditions:
18–24 hours at 36 ±2°C
Incubation Conditions: Evaluation and Typical Results:
18–72 hours at 30–35°C E. coli and coliform bacteria form blue Evaluation and Typical Results:
colonies with a blue surrounding. This color E. coli and coliform bacteria form 1–2 mm
Evaluation and Typical Results: is dark blue at faecal coliforms with strong diameter yellow colonies surrounded
Escherichia coli forms large red or reddish lactose fermentation and lighter blue for by a yellow zone. Non-lactose fermenting
colonies, coliform microbes form large pink, non-faecal coliforms with weaker lactose bacteria develop red or colorless colonies
sometimes slimy colonies, lactose-negative fermentation. Lactose-negative bacteria without yellow zone.
enterobacteria form colorless colonies. grow with different colors and are not
Gram-positive microbes are inhibited. evaluated. Remarks: Higher incubation
temperatures largely suppress the non-
faecal coliforms.

Escherichia coli Escherichia coli Escherichia coli

E. coli and coliforms from river water E. coli and coliforms from waste water E. coli and coliforms from waste water

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3. Other Faecal Bacteria

Tergitol TTC NPS Azide NPS Bismuth Sulfite NPS


Type 14056 Type 14051 Type 14057

Selective and differential medium for For the detection and enumeration of Selective culture medium according to
the detection and enumeration of coliform intestinal enterococci according to Slanetz Wilson and Blair for isolating Salmonella
bacteria and E. coli according to Pollard; and Bartley. Dehydrated culture medium typhi and other salmonellae. Dehydrated
modified acc. to Chapman. Dehydrated for cultivating microorganisms in raw culture medium for cultivating microorgan-
culture medium for cultivating micro­ materials, water (general quality), natural isms in pharmaceuticals, cosmetics, raw
organisms in raw materials, water (general water, waste water, beverages, foods and materials, water (general quality), waste
quality), waste water, beverages, foods other products. water, foods and other products.
and other products.
References: References:
References: APHA (food), APHA (water), EG 98/83, AFNOR, APHA (dairy), APHA (food), AOAC,
APHA (food), EG 98/83, ISO 7704, ISO 8199, HMSO, ISO 7704, ISO 7899-2, ISO 8199, DGHM, FDA, HMSO, ISO 6579 [1981],
ISO 9308-1 [1990], ISO 9308-1 [2001] LMBG, MNO ISO 7704, USDA, USP

Incubation Conditions: Incubation Conditions: Incubation Conditions:


18–24 hours at 36 ±2°C 40–48 hours at 36 ±2°C 40–48 hours at 36 ±2°C

Evaluation and Typical Results: Evaluation and Typical Results: Evaluation and Typical Results:
Lactose-positive microorganisms form Enterococci form red, pink or reddish Most salmonellae form light colored colonies
yellow-orange colonies with a yellow brown colonies with a diameter of with brown to black centers surrounded by a
surrounding and have a yellow dot under 0.5–2 mm. Remarks: Enterococci are black zone with a metallic sheen (“fish eye”).
the membrane filter. According to considered to be indicator organisms Some Salmonella species develop uniformly
ISO 9308-1 all colonies that show yellow of faecal contamination. They are less dark brown to black colonies which may lack
color under the membrane filter are sensitive to chemical effects than are the typical zone. Remarks: If a very slight
counted as positive. Remarks: Tergitol 7 E. coli organisms and are therefore longer contamination with salmonellae is suspected,
inhibits Gram positive colonies and mini- detectable, for instance in waste water prepare a selective enrichment culture and
mizes the swarming of Proteus. Further and in chlorinated water. subsequently streak the sample with an
differentiations of E.coli and coliforms inoculation loop on a membrane filter that
with Oxidase- and Indol-Tests are required. has been placed on the pre-wetted NPS.

Escherichia coli Enterococcus faecalis Salmonella typhosa, streak

E. coli and coliforms from waste water Enterococci from waste water Salmonellae from waste water

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4. Non-faecal, Pathogenic Bacteria 5. Yeasts and Molds

Cetrimide NPS Chapman NPS Lysine NPS


Type 14075 Type 14074 Type 14061

For the detection and enumeration of Mannitol salt medium according to Selective medium for isolating and
Pseudomonas aeruginosa according to Chapman, modified for detecting and enumerating “wild yeasts” in breweries acc.
Lowbury. Dehydrated culture medium for iso­lating pathogenic Staphylococci. to Morris and Eddy. Dehydrated culture
cultivating microorganisms in cosme­tics, Dehydrated culture medium for cultivating medium for cultivating microorganisms in
raw materials, water (general quality), microorganisms in pharmaceuticals, beer and other products.
waste water, foods and other products. cosme­tics, raw materials, water (general
quality), waste water, foods and other References:
References: products. Journal Institute of Brewing, VLB
APHA (water), AOAC, ASM, DIN 38411,
EG 98/83, FDA, ISO 7704, ISO 8199, References: Incubation Conditions:
EN 12780, EN ISO 16266 APHA (food), AOAC, DGHM, FDA, HMSO, 3–5 days at 30–35°C
ISO 7704, USP
Incubation Conditions: Evaluation and Typical Results:
40–48 hours at 36 ±2°C Incubation Conditions: Only “wild yeasts” (not belonging to the
18–72 hours at 30–35°C genus Saccharomyces) which utilize
Evaluation and Typical Results: lysine as sole source of nitrogen grow on
Pseudomonas aeruginosa forms blue, Evaluation and Typical Results: this medium, they form white or cream
blue-green or yellow-green colonies Staphylococcus aureus forms yellow colored colonies; brewery culture yeasts
with 1–2 mm diameter and blue zones. colonies with a yellow surrounding grow not at all or very poorly.
The colonies produce pyocyanin and (mannitol-positive). Other Staphylococci
fluorescein and show fluorescence in grow without zones of color change.
UV-light. Other Pseudomonads develop Most other bacteria are inhibited.
colonies with different colors. Remarks:
Further tests are necessary for definitive
identi­fication of Ps. aeruginosa.

Pseudomonas aeruginosa Staphylococcus aureus Torulopsis spec.

Mixed culture with Pseudomonas aeruginosa Mixed culture of staphylococci “Wild yeasts” from lager beer

14
5. Yeasts and Molds

Malt Extract NPS Sabouraud NPS Schaufus Pottinger


Type 14086 Type 14069 (m Green yeast and mold) NPS
Type 14070; 14072; 14080; 14083; 14091.
For the isolation and enumeration of yeasts For the cultivation and enumeration of
and molds. Dehydrated culture medium for yeasts and molds. Dehydrated culture M Green Yeast and Mold medium for the
cultivating microorganisms in beverages, medium for cultivating microorganisms in detection of yeasts and molds according
wine, soft drinks, concentrates, fruit juice, pharmaceuticals, cosmetics, raw materials, to Schaufus and Pottinger. Dehydrated
foods and other products. water (general quality), waste water and culture medium for cultivating microor-
other products. ganisms in wine, soft drinks, concentrates,
References: sugar, sugar products and other products.
APHA (food), AOAC, IFU References:
APHA (food), AOAC, EP, USP Incubation Conditions:
Incubation Conditions: 2–5 days at 20–25°C or at 30–35°C
3–5 days at 20–25°C or at 30–35°C Incubation Conditions: depending on the target of the
depending on the target of the investigation < 5 days at 20–25°C investigation

Evaluation and Typical Results: Evaluation and Typical Results: Evaluation and Typical Results:
Yeasts normally develop smooth white, Yeasts usually develop smooth white or Molds develop velvety or fluffy whitish or
rarely colored colonies. Molds generally colored colonies. Molds form velvety greenish colonies which can get various
form velvety or fluffy, cotton-like colonies or fluffy, cotton-like colonies that are colors after conidiospore production. Yeasts
that are white during the early growth white in the early growth phase and may have a smooth surface. Acid forming sugar
phase and later, after conidiospore forma- take various colors after conidiospore fermenters are whitish to yellow, non-acid
tion, of various colors. Remarks: The low production. Remarks: According to formers are, by contrast, greenish to blue-
pH of this medium suppresses the growth the EP | USP antibiotics could be added green. Remarks: The low pH suppresses the
of most bacteria. This medium is available immediately before use. growth of most bacteria. This medium is
with two different types of membrane available with various types of membrane
filters. filters: 3 different pore sizes and 2 different
colors.

Saccaromyces cerevisiae Alternaria humicola Torula lipolytica

Mixed culture from Saccaromyces and Rhodutorula Yeasts and molds from cough syrup Mixed culture from a soft drink

15
6. Product-spoiling
Microorganisms

Wallerstein (WL Nutrient) NPS Wort NPS Glucose Tryptone NPS


Type 14089 Type 14058, 14092 Type 14066

For the detection and enumeration of the For the detection and determination of For the enumeration of mesophilic and
microbiological flora of brewing and fer- yeasts and molds. Dehydrated culture thermophilic bacteria, especially “flat-sour”
mentation processes acc. to Green and Gray medium for cultivating microorganisms microorganisms in canned foods.
(1950). Dehydrated culture medium for in raw materials, beverages, beer, wine,
cultivating microorganisms in beverages, soft drinks, concentrates, foods and other References:
beer, wine, soft drinks, concentrates, fruit products. APHA (dairy), APHA (food), AOAC, ICUMSA,
juice and other products. IFU, ISO 7704, NCA
References:
References: VLB Incubation Conditions:
ISO 7704 18–72 hours at 30–35°C for mesophilic
Incubation Conditions: bacteria; 48–72 hours at 55 ±2°C for
Incubation Conditions: 3–5 days at 20–25°C or at 30–35°C thermophilic sporulating microorganisms
2–5 days at 30–35°C aerobic or anaerobic depending on the target of the
depending on the target of the investigation investigation Evaluation and Typical Results:
Microorganisms that ferment glucose
Evaluation and Typical Results: Evaluation and Typical Results: and produce acid grow as yellowish green
Yeasts usually grow as yellowish green Yeasts usually develop smooth white or colonies. “Flat-sour” colonies have a
colonies. Molds generally form velvety or colored colonies. Molds generally form diameter of 2-5 mm, a yellowish-green
fluffy cotton-like colonies that look white velvety or fluffy cotton-like colonies that color and are surrounded by a yellow zone.
in the early growth phase and may take look white in the early growth phase and Remarks: For the incubation at 55 ±2°C the
various colors after conidiospore produc- may take various colors after conidiospore petri dishes must be placed into a moist
tion. Bacteria grow slowly and their colonies production. chamber.
are of different size and color. Remarks:
The addition of 0.004 g/l cycloheximide to
the wetting solution makes the medium
selective for lactic acid bacteria, the growth
of yeasts and molds is suppressed.

Saccharomyces cerevisiae Saccharomyces cerevisiae Bacillus coagulans, the “flat sour” colony

Lactobacillus plantarum Yeasts and molds from spoiled beer Mixed culture from canned vegetables

16
6. Product-spoiling
Microorganisms

Jus de Tomate (Tomato Juice) NPS Orange Serum NPS VLB-S7-S NPS
Type 14079 Type 14062; 14096 Type 14059

For the detection of product spoiling lactic For the isolation and enumeration of For the detection of pediococci and lacto­
acid bacteria especially Oenococcus oeni acid-tolerant microorganisms. Dehydrated bacilli according to Emeis; modified acc.
acc. to Dubois, Bindan and Lafon-Lafour- culture medium for cultivating micro­ to Rinck and Wackerbauer. Dehydrated
cade. Tight-fitting, special petri dishes for organisms in raw materials, water (general culture medium for cultivating micro­
micro­aerophilic incubation. Dehydrated cul- quality), waste water, wine, soft drinks, organisms in beer and other products.
ture medium for cultivating microorganisms concentrates, fruit juice, foods and other
in wine, fruit juice and other products. products. References:
EBC, ISO 7704, MEBAC, VLB
References: References:
ISO 7704, Lanaridris& Lafon-Lafourcade APHA (water), IFU, ISO 7704, MPP Incubation Conditions:
(packaging staff) 3–5 days at 30–35°C anaerobic
Incubation Conditions: (microaerophil)
5–7 days at 30–35°C anaerobic Incubation Conditions:
(microaerophil); control for slowly 3–5 days at 30–35°C aerobic or Evaluation and Typical Results:
growing micro-organisms after anaerobic depending on the target of Pediococci (“Sarcina”) develop round pale
10 days is recommended the investigation green colonies with smooth peripheries
and approx. 1 mm in diameter. Lactobacilli
Evaluation and Typical Results: Evaluation and Typical Results: grow as slightly rounded, irregularly lobed
Lactobacilli form compact, whitish to Only acid-tolerant microorganisms can colonies with approx. 2 mm in diameter
slightly yellowish colonies with 1–3 mm grow on this medium such as lactic acid which are initially light green and later
diameter. Pediococci develop somewhat bacteria (Lactobacillus, Pediococcus etc.), dark green. Remarks: This medium must
smaller colonies with approx. 1 mm dia­ acetic acid bacteria, yeasts and molds. be incubated under anaerobic to micro-
meter that later get a whitish to slightly Remarks: This medium is available with aerophilic conditions.
brownish color. Oenococcus oeni grows pH 5.5 and with pH 3.2.
as colorless to whitish colonies with a
diameter smaller than 1 mm. Remarks:
This medium must be incubated under
anaerobic to micro­aerophilic conditions.

Lactic-acid bacteria, streak Rhodotorula spec. Lactobacillus brevis

Oenococcus oeni from wine Mixed culture from a soft drink Lactobacilli and pediococci from sediment, streak

17
6. Product-spoiling
Microorganisms

Weman NPS MRS NPS


Type 14065 Type 14077

For the detection and determination of For the detection of different Lactobacillus
slime-forming mesophilic bacteria accord- species and other lactic acid bacteria
ing to Weman, modified acc. to Lorenz. according to DE MAN, ROGOSA and
Dehydrated culture medium for cultivating SHARPE. Dehydrated culture medium
microorganisms in soft drinks, concen- for the isolation and cultivation of Lacto-
trates, sugar, sugar products and other bacillus from dairy and food products.
products.
References:
References: APHA (food, dairy products)
ICUMSA, ISO 7704
Incubation Conditions:
Incubation Conditions: 3–5 days at 30°C anaerobic conditions
3–5 days at 30–35°C
Evaluation and Typical Results:
Evaluation and Typical Results: The MRS NPS are used for the detection
The colonies of slime-forming mesophilic of a variety of Lactobacilli. The Lactobacilli
bacteria are smooth, round, usually species grow as slightly rounded whitish
colorless and transparent or translucent. colonies with approximately 1–2 mm in
Some have a diameter greater than 5 mm. diameter. Other microorganisms, which
have not this typical growth, can be
defined by confirmation tests. Lactobacilli
species are gram positive, Katalase negative
and negative in the production of Indole
and Hydrogen sulfide.

Leuconostoc mesenteroides Lactobacillus brevis

Mixed culture from sugar syrup

18
Troubleshooting Guide
If the directions for use are not beeing – contamination during preparation
followed this may lead to unsatisfactory
– microbes rinsed off the membrane filter
results listed below:
by incomplete vacuum filtration of
the sample or rinse liquid or by tilting
1. Inhibited Growth, Tiny Colonies
the prepared petri dish
– pad too dry: not enough water used
– contaminated filter support
2. Colonies Run – contaminated forceps
– pad too wet, water film on the
4. Growth on One Side Only
membrane filter: too much water used.
– petri dish slanted in the incubator
– Colonies of motile microbes (such as
Bacillus or Proteus) tend to run even
5. Too Profuse or too Sparse Growth
though the water dosage is correct. To
(optimum microbial number between
prevent this, add NaCI or an emulsifier.
20 and 200 per filter)
3. Contamination from Underneath – wrong dilution selected or sample
inadequately mixed with the diluent.
Inhibited colony growth, excess ring
of liquid cloudy, often including
6. Non-uniform Growth
discoloration of the pad:
– sample volume less than 5 ml filtered
– membrane placed with grid facedown
without adding sterile NaCl-buffer­
on the pad instead of faceup
solution as a diluent or sample volume
– contamination during rehydration inadequately mixed with the diluent.
(by airborne microbes, by contact or
by contaminated water)

Membrane Filters for Use on


Agar Plates or on Adsorbent Pads
If agar plates or absorbent pads to be The membrane filters are available indivi-
wetted with liquid culture medium are ually packaged and sterilized or packaged
used instead of Nutrient Pad Sets, we in a special designed individual package
recommend Sartorius Stedim Biotech on a band for the use with the Microsart®
cellulose nitrate (cellulose ester) mem- e.motion membrane filter dispenser.
brane filters. These membranes are The certificate included in every package
offered in a choice of three different documents the quality assurance tests
colors to suit your specific test applica- as well as the compliance of the 0.45 µm
tion, and provide a high-contrast membrane filters with ISO 7704.
background. For simple evaluation of
the results, a grid divides the filtration
area into 130 squares, each measuring
3.1 + 3.1 mm.

19
Membrane Filters for Use on Agar Plates or on Absorbent Pads
For Detection of Bacteria Providing Optimal Contrast to Light- For Detection of Yeasts
in Dyed Media. colored or Transparent Bacteria Colonies. and Molds.

White Membrane with Black Grid Green Membrane with Dark Green Grid Grey Membrane with White Grid
Pore Size d Pckg. Size Order No. Pore Size d Pckg. Size Order No. Pore Size d Pckg. Size Order No.
0.2 µm 47 100 11407-47-ACN* 0.45 µm 47 100 13806-47-ACN* 0.45 µm 47 100 13006-47-ACN*
47 1,000 11407-47-ACR* 47 1,000 13806-47-ACR* 47 1,000 13006-47-ACR*
50 100 11407-50-ACN* 50 100 13806-50-ACN* 50 100 13006-50-ACN*
50 1,000 11407-50-ACR 50 1,000 13806-50-ACR* 50 1,000 13006-50-ACR
0.45 µm 47 100 11406-47-ACN* 0.65 µm 47 100 13005-47-ACN*
47 1,000 11406-47-ACR* 50 100 13005-50-ACN*
50 100 11406-50-ACN* 50 1,000 13005-50-ACR
50 1,000 11406-50-ACR* 0.8 µm 47 100 13004-47-ACN*
HighFlow 47 1,000 13004-47-ACR
0.45 µm 47 100 114H6-47-ACN 50 100 13004-50-ACN*
47 1,000 114H6-47-ACR 8 µm 47 100 13001-47-N
50 100 114H6-50-ACN (non-sterile)
50 1,000 114H6-50-ACR 50 100 13001-50-N
0.65 µm 47 100 11405-47-ACN* (non-sterile)
50 100 11405-50-ACN
0.8 µm 47 100 11404-47-ACN* Prefilters, White Without Grid
47 1,000 11404-47-ACR 11301, a white membrane filter with a
50 100 11404-50-ACN* pore size of 8 µm is used as a prefilter in
1.2 µm 47 100 11403-47ACN* a special prefilter attachment (16807) for
47 1,000 11403-47ACR bacterio­logical analyses. It retains coarse
50 100 11403-50ACN* suspended particles, whereas it allows
50 1,000 11403-50ACR microorganisms to pass through. These
microbes are trapped on the surface of the
White Membrane with Green Grid underlying bacteria-retentive membrane
HighFlow filter. Order no.: 11301--47----ACN and
Pore Size d Pckg. Size Order No. 11301--50----ACN.
0.45 µm 47 100 13906-47-ACN* The special pore structure of the
47 1,000 13906-47-ACR* 0.45 µm HighFlow membrane
50 100 13906-50-ACN* filters allow shorter filtration
50 1,000 13906-50-ACR* times due to higher flow rates
and throughputs. Especially E. coli
HighFlow shows best growth promotion on
0.45 µm 47 100 139H6-47-ACN HighFlow membranes.
47 1,000 139H6-47-ACR
50 100 139H6-50-ACN As every Sartorius Stedim Biotech
0.45 µm membrane filter lot these
0.65 µm 47 100 13905-47-ACN membranes are also tested and * Also available as a non-sterile version.
To order boxes with 100 pcs. replace ACN with N
1.2 µm 47 100 13903-47-ACN released according to ISO 7704. and for boxes of 1,000 pcs. replace ACR with R.

Other types on request

20
Membrane Filters for Use with Microsart® e.motion Dispenser
For Detection of Bacteria Providing Optimal Contrast to Light- For Detection of Yeasts
in Dyed Media. colored or Transparent Bacteria Colonies. and Molds.

White Membrane with Black Grid Green Filter with Dark Green Grid Grey Filter with White Grid
Pore d Pckg. Order No. Pore d Pckg. Order No. Pore d Pckg. Order No.
Size Size Size Size Size Size
0.2 µm 47 3 + 100 11407Z-47----SCM 0.2 µm 47 3 + 100 15407Z-47----SCM HighFlow
50 3 + 100 11407Z-50----SCM 0.45 µm 47 3 + 100 13806Z-47----SCM 0.45 µm 47 3 + 100 130H6Z-47----SCM
HighFlow 50 3 + 100 13806Z-50----SCM 0.45 µm 47 3 + 100 13006Z-47----SCM
0.45 µm 47 3 + 100 114H6Z-47----SCM 50 3 + 100 13006Z-50----SCM
50 3 + 100 114H6Z-47----SCM 0.65 µm 47 3 + 100 13005Z-47----SCM
0.45 µm 47 3 + 100 11406Z-47----SCM 50 3 + 100 13005Z-50----SCM
50 3 + 100 11406Z-47----SCM 0.8 µm 47 3 + 100 13004Z-47----SCM
0.8 µm 47 3 + 100 11404Z-47----SCM 50 3 + 100 13004Z-50----SCM
1.2 µm 47 3 + 100 11403Z-47----SCM
50 3 + 100 11403Z-50----SCM

White Membrane with Green Grid


Pore d Pckg. Order No.
Size Size
0.45 µm 47 3 + 100 13906Z-47----SCM
50 3 + 100 13906Z-50----SCM
HighFlow
0.45 µm 47 3 + 100 114H6Z-47----SCM
50 3 + 100 114H6Z-47----SCM

HighFlow
The special pore structure of the
0.45 µm HighFlow membrane
filters allow shorter filtration
times due to higher flow rates
and throughputs. Especially E. coli
shows best growth promotion on
HighFlow membranes.
As every Sartorius Stedim Biotech
0.45 µm membrane filter lot these
membranes are also tested and
released according to ISO 7704.

21
Typical Application Examples
Product Detection and Enumeration of... Nutrient Pad Type
Beer Lactobacilli and Pediococci and other beer spoiling organisms VLB-S7-S, MRS
Total colony count Standard, Standard TTC
Wild yeasts Lysine
Yeasts and molds Malt Extract*, Wallerstein Nutrient, Wort
Dairy Latic Acid Bacteria | Lactobacillaceae MRS
Foods Acid-tolerant microorganisms Orange Serum
Enterobacteria, E. coli and coliforms CHROMOCULT ® **, ECD, Endo, (MacConkey), m FC, Teepol |
Lauryl Sulphate, Tergitol TTC
Enterococci, Enterococcus faecalis Azide | KF Strep
Lactobacilli MRS
Pseudomonas aeruginosa Cetrimide
Salmonellae Bismuth Sulfite
Staphylococci, Staphylococcus aureus Chapman
Thermophilic spore formers and mesophilic bacteria Glucose Tryptone
Total colony count Caso, Standard, Standard TTC, TGE | Tryptone Glucose Extract
Yeasts and molds Malt Extract, Wort
Food & beverage Lactobacilli MRS
Fruit juice Enterobacteria, E. coli and coliforms Endo, (MacConkey), Tergitol TTC*
Lactobacilli MRS
Oenococcus and other product spoiling organisms Jus de Tomate | Tomato Juice, Orange Serum
Yeasts and molds Malt Extract, Schaufus Pottinger | m Green yeast and mold,
Wallerstein Nutrient, Wort
Milk E. coli and coliforms Endo
Enterococci, Enterococcus faecalis Azide | KF Strep
Salmonellae Bismuth Sulfite
Pharmaceuticals, WFI, Enterobacteria, E. coli MacConkey
raw materials and cosmetics Enterococci, Enterococcus faecalis Azide | KF Strep
Pseudomonas aeruginosa Cetrimide (cosmetics only)
Staphylococci, Staphylococcus aureus Chapman
Total colony count Caso, R2A
Yeasts and molds, Candida albicans Sabouraud
Soft drinks, concentrates Acid-tolerant microorganisms, Lactic-acid bacteria Orange Serum, VLB-S-7-S
Enterobacteria, E. coli and coliforms Endo, MacConkey
Lactobacilli MRS
Mesophilic slime-forming bacteria, Leuconostoc Weman
Total colony count Standard*, Standard TTC*, TGE | Tryptone Glucose Extract
Yeasts and molds Malt Extract, Schaufus Pottinger | m Green yeast and mold,
Wallerstein Nutrient, Wort
Sugar, sugar products E. coli and coliforms Endo
Mesophilic slime-forming bacteria, Leuconostoc Weman
Thermophilic spore formers and mesophilic bacteria Glucose Tryptone
Yeasts and molds Malt Extract*, Schaufus Pottinger | m Green yeast and mold, Wort*
Water (general quality), Acid-tolerant microorganisms, Lactic-acid bacteria Orange Serum
mineral water, natural water, Enterobacteria, E. coli and coliforms CHROMOCULT ® **, ECD, Endo, (MacConkey), m FC, Teepol |
waste water Lauryl Sulphate, Tergitol TTC
Enterococci, Enterococcus faecalis Azide | KF Strep
Pseudomonas aeruginosa Cetrimide
Salmonellae Bismuth Sulfite
Staphylococci, Staphylococcus aureus Chapman
Total colony count Caso, R2A, Standard, Standard TTC, TGE | Tryptone Glucose Extract,
Yeast Extract
Yeasts and molds, Candida albicans Sabouraud
Wine Acetobacter Orange Serum, Wort (both wetted with 5-8% ethanol)
Acid-tolerant microorganisms, Lactic-acid bacteria Orange Serum
Lactobacilli MRS
Oenococcus and other wine spoiling organ. Jus de Tomate | Tomato Juice
Yeasts and molds Malt Extract, Schaufus Pottinger | m Green yeast and mold,
Wallerstein Nutrient, Wort
* T hese NPS types are suitable for the determination of the mentioned microorganisms, although the media are not explicit declared
in the references described in this publication.
22 ** Trade mark owner and manufacturer is Merck KGaA
Growth Comparison
The principle of the membrane filter variance in allocation of the pores, not all
method is based on the concentration membranes guarantee sufficient nutrient
of micro­organisms from relatively large supply. A comparison of Sartorius Stedim
samples on the surface of a membrane Biotech cellulose nitrate (cellulose mixed
filter. Nutrients and metabolites are ester) membranes with other mixed ester
exchanged through the pore system of membranes reveals significant differences
the membrane filter. The pore size alone in growth promotion results.
is not a meaningful criterion. Due to the

Growth of E. Coli Growth of Pseudomonas Aeruginosa


on Endo NPS on Cetrimide NPS

Sartorius Stedim Biotech cellulose nitrate membrane Sartorius Stedim Biotech cellulose nitrate membrane

E. coli forms red colonies with a metallic Pseudomonas aeruginosa forms blue,
sheen. Other coliforms would grow as blue-green or yellow-green colonies with
dark to light red colonies without metallic 1–2 mm diameter and blue zones. The colo-
sheen. nies produce pyocyanin and fluorescein
and show fluorescence in UV-light. Other
Pseudomonads would develop colonies
with different colors.

Mixed esters membrane Mixed esters membrane

E. coli shows no metallic sheen on this On this mixed esters membrane grow less
mixed ­esters membrane. Therefore it is very colonies and without the blue zone. Due to
difficult to differenciate between E. coli the variance in the allocation of the pores,
and coliforms without any further test. A here the mixed esters membrane did not
quantitative statement is difficult due to guarantee a sufficient nutrient supply. This
the fact of running colonies on the mixed may cause in false negative results.
esters membrane surface.

23
Accessories

Combi.jet Manifold plus Microsart® Combisart® 3-Branch Manifold Plus Combisart® 3-Branch Manifold Plus
Funnel 100 and Microsart® e.jet Biosart® 250 Funnels Biosart® 100 Monitors
Transfer Pump The Biosart 250 Funnel has been designed Biosart 100 Monitors are sterile disposables
Microsart Funnel 100 | 250 are sterile for microbiological quality assurance in with an incorporated membrane filter and
100 ml & 250 ml funnels. The optimal industry. The sterile 250 ml (50 ml gradua- cellulose pad. They are ready-to-use and
sealing is guaranteed by a click-fit closure. tions) plastic funnel guarantees fast filtra- after filtration, the funnel will be removed,
The large inner diameter ensures a high tion and high sample throughputs during so the lid and the base fit to a petri dish.
flow rate and the optimized shape allows a routine testing. Its large inner diameter Each box contains 48 units with 47 mm,
thorough rinsing of the system subsequent allows high flow rates, and the tapered gridded membrane filters.
to the filtration. No liquid is retained in inner wall permit thorough flushing of
the funnel. the funnel, after filtration. 16401-47-07-ACK Biosart 100 Monitor,
individually sterile-
16A07--10------N Microsart Funnel 100, 16407-25-ALK Biosart 250 Funnels, packaged, 0.2 µm
sterile in 5 sealed bags 50 units, sterile-packaged white | black grid
16A07--25------N Microsart funnel 250, 16407-25-ACK Biosart 250 Funnels, 16401-47-06-ACK Biosart 100 Monitor,
sterile in 6 sealed bags 50 units, individually individually sterile-
166MP-4 Microsart e.jet sterile-packaged packaged, 0.45 µm
Transfer pump white | black grid
16848-CJ Microsart Combi.jet For further infomation about our 16402-47-06-ACK Biosart 100 Monitor,
2-fold manifold Combisart manifolds and accessories, individually sterile-
please consider our Combisart brochure. packaged, 0.45 µm
green | dark green grid
16403-47-06-ACK Biosart 100 Monitor,
individually sterile-
packaged, 0.45 µm
grey | white grid
16414 Biosart 100 Adapter
(altern. 16424)

24
Combisart® Individual Systems and Vacuum Pumps, Water Traps and Stainless Steel Prefilter Attachment
Filter Holders Vacuum Hose For removal of coarse particulate sub­
For low number of samples to test, the The vacuum pumps are neoprene stances from samples in a single step
individual system is ideal to use. In this membrane pumps with low noise level, along with bacteria-retentive filtration
equipment set-up, you simply use a silicone oil- and maintenance-free, reliable sources for subsequent microbiological testing.
stopper and a single base to fit your choice of vacuum. The water traps are preventing Clips between a filter support (16840 or
of funnel type on a suction flask. an overflow of filtrate into the vacuum 16841) and a stainless steel funnel (as
pump. show at the photo) or Biosart 250 Funnel.
16841 Stainless steel single base Autoclavable and can be flamed.
6981065 Stainless steel funnel, 100 ml 16694-2-50-22 Microsart® maxi.vac for
6981002 Stainless steel funnel, 500 ml multiple filtration runs, 16807 Prefilter attachment
17575-ACK Minisart® SRP 25, 50 sterile 230 V, 50 Hz
venting filters 16694-1-60-22 Microsart® maxi.vac,
17173 Silicone stopper 115 V, 60 Hz
16672 Suction flask 16694-2-50-06 Microsart® mini.vac
for single filtration run,
Alternatively to position 1–3 you can 230 V, 50 Hz
use 16219-CS as 100 ml filter holder or 16694-1-60-06 Microsart® mini.vac,
16201-CS as 500 ml filter holder. 115 V, 60 Hz
17804-M Vacusart®, 3 individually
sterile-packaged PTFE
filter
166MP-4 Microsart® e.jet Transfer
Pump
16610 Woulff‘s bottle, 500 ml,
with stop cock
16623 Rubber vacuum hose, 1 m

25
Dosing Syringe | Colony Counter Microsart® e.motion Dispenser – Microsart® e.motion Membrane Filters
The most convenient way to moist the Membrane Filters on Demand The cellulose nitrate (cellulose mixed ester)
NPS with water is to use a dosing syringe The completely new membrane filter membranes suitable for the use in dispens-
with an adapted Minisart syringe filter. dispenser meets all requirements placed ers are sterile-sealed, without protective
Simultaneous sterilization and dosing of on advanced laboratory equipment. paper on top of each filter, in a specially
demineralized water in 3.5 ml steps is easy The membrane filters are released from designed individual package on a band.
done by dropping the sinker at the end their sterile packaging fully automa­tically The special pleating of the band of mem-
of the suction tubing into the water, at the touch of a button or hands-free – brane filter units ensures that they are
and the dosing syringe filled and dosed a dispensing operation is triggered when perfectly flat when dispensed. The shape
by operating the twigger auto­matically. the optical sensor detects approaching of the sealed band guarantees uniform
tweezers. dispensing of the individual membrane
Compact battery operated colony counter, filters.
is as simple to use as a ball-point pen, and 16712 Microsart® e.motion Dispenser
has a 4-digit LCD-display. 11407Z-47----SCM white | black, 0.2 µm
114H6Z-47----SCM white | black, 0.45 µm
16685-2 Dosing syringe High Flow
17597k Minisart®, 0.2 µm, individually 11406Z-47----SCM white | black, 0.45 µm
sterile-packaged 139H6Z-47----SCM white | green, 0.45 µm
17649 Colony Counter High Flow
13906Z-47----SCM white | green, 0.45 µm
13806Z-47----SCM green | dark green,
0.45 µm
13006Z-47----SCM gray | white, 0.45 µm
130H6Z-47----SCM gray | white, 0.45 µm
High Flow
13005Z-47----SCM gray | white, 0.65 µm
15407Z-47----SCM green | dark green,
0.2 µm

26
Absorbent Pads AirPort MD8 arium® Laboratory Water Systems
The 1.4 mm thick absorbent pads are AirPort MD8 uses the gelatin membrane A choice of more than 70 arium® versions is
wetted with the appropriate liquid culture filter method guaranteeing reliable and available to meet all your requirements on
medium before a membrane filter is placed exact measurement results. It is battery- water quality and to cover any application.
on. Each box contains 1,000 absorbent powered and portable for universal use. Whether for standard applications, routine
pads in 10 tubes, each with 100 pads, analysis or critical applications where
and with manual dispensing device, all 16757 AirPort MD8, 100-240 V, reagent-grade water is required, the arium®
presterilized. 47-63 Hz, complete series consistently supplies highest water
with holder and battery quality for your application.
15410-47-ALR Absorbent pads, 47 mm, charger
each approx. 3 ml 17528-80-ACD Gelatin membranes, proDI Standard applications, e.g. buffer
absorbent capacity individually sterile- preparation
15410-50-ALR Absorbent pads, 50 mm, packaged, each in 1 bag proUV Low TOC applications e.g. HPLC
each approx. 3.5 ml 17528-80-BZD Gelatin membranes, proUF Low endotoxin applications
absorbent capacity individually sterile- proVF Low TOC and low endotoxin
13906-47-APR Absorbent pads, 47 mm, packaged, each in 3 bags applications
including membrane
filters 0.45 µm, white |  Further laboratory water systems on
green grid, individually request.
sterile-packaged

27
Technical Data and Application Guide Nutrient Pad Sets
Detection Target and Reference1) Test Sample Materials Media Type (pH) Recom.
Order No. (Filter Type)2), 3) Incubtion Conditions4)

Counting of Total Colony Forming Units


Total count
APHA (dairy), APHA (food), APHA (water), Pharmaceuticals, cosmetics, raw materials, Caso (pH 7.3) Bacteria:
AOAC, DAB, EG 98/83, EP, FDA, IDF, water (general quality), waste water, foods, 14063--47------N (1) < 3 d at 30–35°C;
ISO 7704, ISO 8199, ISO 9308-1 [1990], other products. Yeasts and molds:
ISO 9308-1 [2001], USDA, USP. < 5 d at 30–35°C
Total count
APHA (water), EP, ISO 7704. Water for pharma purpose, water R2A (pH 7.2) > 5 d at 30–35°C
(general quality), waste water, 14084--47------N (1)
other products. 14084--47----RDN
Total count
APHA (water), ISO 7704, VLB. Raw materials, water (general quality), Standard (pH 7.2) < 5 d at 30–35°C
waste water, beverages, beer, foods, 14064--47------N (1)
other products.
Total count
APHA (water), ISO 7704, VLB. Raw materials, water (general quality), Standard TTC (pH 7.2) < 5 d at 30–35°C
natural water, waste water, beverages, beer, 14055--47------N (1)
foods, other products.
Total count
APHA (water), ISO 7704, VLB. Raw materials, water (general quality), Standard TTC I mod. < 5 d at 30–35°C
natural water, waste water, beverages, beer, (pH 7.2)
foods, other products. 14085--47------N (1)
14085--47----RDN
Total count
APHA (dairy), APHA (food), APHA (water), Raw materials, water (general quality), TGE | Tryptone Glucose < 5 d at 30–35°C
API, ISO 7704. natural water, waste water, beverages, soft Extract (pH 7.0)
drinks, concentrates, foods, other products. 14076--47------N (1)
14076--47----RDN
Total count
EG 98/83, HMSO, ISO 6222, ISO 7704, Water (general quality), natural water, Yeast Extract (pH 7.2) 44 ±4 h at 36 ±2°C;
ISO 8199. other products. 14090--47------N (1) 68 ±4 h at 22 ±2°C

E. Coli and Coliforms, Enterobacteria


E. coli and coliforms
ISO 7704, Journal Food Protection, Raw materials, water (general quality), CHROMOCULT ® * (pH 7.0) 20–28 h at 36 ±2°C
ZenHyg (journal of hygiene). waste water, beverages, foods, 14087--47------N (7)
other products. 14087--47----RDN
E. coli
APHA (water), DIN 10110, EG 98/83, Raw materials, water (general quality), ECD (pH 7.0) 16–18 h at 44 ±2°C
ISO 7704, ISO 8199, ISO 9308-1 [2001], waste water, beverages, foods, 14082--47------N (2)
LMBG, USDA. other products.
E. coli and coliforms
APHA (dairy), APHA (food), APHA (water), Raw materials, water (general quality), Endo (pH 7.4) 18–24 h at 36 ±2°C
DGHM, ISO 7704, ISO 9308-1 [1990], natural water, waste water, beverages, 14053--47------N (9)
MNO, USDA. soft drinks, concentrates, fruit juice, sugar, 14053--47----RDN
sugar products, foods, other products.
E. coli and coliforms
APHA (food), APHA (water), AOAC, EPA, Raw materials, water (general quality), m FC (pH 7.4) 18–24 h at 36 ±2°C
FDA, ISO 7704, ISO 9308-1 [1990], USDA. waste water, beverages, foods, 14068--47------N (2)
other products. 14068--50----PDN
(closed petri dishes) (2)
Enterobacteria, E. coli
APHA (dairy), APHA (food), APHA (water), Pharmaceuticals, cosmetics, raw materials, MacConkey (pH 7.1) 18–72 h at 30–35°C
AOAC, DAB, DIN 38411, DGHM, water (general quality), natural water, waste 14097--47------N (2)
EP, ISO 7704, LMBG, MNO, USDA, USP. water, beverages, soft drinks, concentrates,
fruit juice, foods, other products.

28
1)
Shelf Life Test Strains5) Reference Guide on page 34.
2)
A Set contains 100 Nutrient Pads and
100 membrane filters, both individually, sterile
packaged. The membrane filters are selected
for optimum growth together with the
corresponding nutrient media. The supplied
24 01, 03, 05, 09, 18, 22, 25, 26 membrane filter type is listed within brackets:
(1) = green with dark green grid,
0.45 µm pore size
(2) = white with green grid, 0.45 µm pore size
(3) = gray (after wetting black) with white grid,
24 01, 03, 05, 09, 18, 22, 26 0.65 µm pore size
(4) = white with green grid, 0.65 µm pore size
(5) = white with green grid, 1.2 µm pore size
(6) = gray (after wetting black) with white grid,
0.8 µm pore size
24 03, 07, 09, 18, 26 (7) = white with black grid, 0.45 µm pore size
(8) = gray (after wetting black) with white grid,
0.45 µm pore size
(9) = white with green grid, 0.45 µm pore size,
High Flow (ideal for E. coli)
24 03, 07, 09, 18, 26 (10) = gray (after wetting black) with white grid,
0.45 µm pore size, High Flow
3)
Diameter of the membrane filter, 47 mm.
Order number for Nutrient Pad Sets
24 03, 07, 09, 18, 26
with 50 mm membrane filter as above, but
--47------N replaced by --50------N.
Most of the NPS types are also available with
Microsart® e.motion Membrane Filters:
Order number as above, but ---N replaced by
24 09, 18, 26 -RDN.
Other NPS types and NPS with
Microsart® e.motion Membrane Filters on request.
4)
The incubation conditions are recommended
24 03, 07, 09, 18, 26 by Sartorius Stedim Biotech. They may be varied
according to the type of samples in compliance
with the reference standard or customer’s
requirements.
5)
Test strains on page 32.
24 06, 09, 11, 21, 25 * Trade mark owner and manufacturer
is Merck KGaA

24 06, 09, 19, 21, 22

24 06, 07, 09, 21, 25, 28

24 06, 07, 09, 11, 21

24 02, 06, 09, 21, 25, 26

29
Detection Target and Reference1) Test Sample Materials Media Type (pH) Recom.
Order No. (Filter Type)2), 3) Incubtion Conditions4)
E. coli and coliforms
AFNOR, APHA (water), BS, FDA, ISO 7704, Water (general quality), waste water, Teepol | Lauryl Sulphate 18–24 h at 36 ±2°C
ISO 9308-1 [1990], USDA. beverages, foods, other products. (pH 7.2)
14067--47------N (2)
14067--47----RDN
E. coli and coliforms
APHA (food), EG 98/83, ISO 7704, Raw materials, water (general quality), Tergitol TTC (pH 8.0) 18–24 h at 36 ±2°C
ISO 8199, ISO 9308-1 [1990], waste water, beverages, foods, 14056--47------N (2)
ISO 9308-1 [2001]. other products. 14056--47----RDN

Other Faecal Bacteria


Enterococci
APHA (food), APHA (water), EG 98/83, Raw materials, water (general quality), Azide | KF Strep 40–48 h at 36 ±2°C
HMSO, ISO 7704, ISO 7899-2, ISO 8199, natural water, waste water, beverages, (pH 7.2 ±0.1)
LMBG, MNO. foods, other products. 14051--47------N (1)
14051--47----RDN
Salmonellae
AFNOR, APHA (dairy), APHA (food), AOAC, Pharmaceuticals, cosmetics, raw materials, Bismuth Sulfite (pH 7.6) 40–48 h at 36 ±2°C
DGHM, FDA, HMSO, IDF, ISO 6579 [1981], water (general quality), waste water, foods, 14057--47------N (1)
ISO 7704, USDA. other products.

Non-faecal, Pathogenic Bacteria


Pseudomonas aeruginosa
APHA (water), AOAC, ASM, DIN 38411, Cosmetics, raw materials, water Cetrimide (pH 7.1) 40–48 h at 36 ±2°C
EG 98/83, FDA, ISO 7704, ISO 8199, (general quality), waste water, foods, 14075--47------N (2)
ISO 16266. other products. 14075--47----RDN
Staphylococci, Staph. aureus
APHA (food), AOAC, DGHM, FDA, HMSO, Pharmaceuticals, cosmetics, raw materials, Chapman (pH 7.4) 18–72 h at 30–35°C
ISO 7704, USP. water (general quality), waste water, foods, 14074--47------N (2)
other products.

Yeasts and Molds


Wild yeasts
Journal Institute of Brewing, VLB. Beer, other products. Lysine (pH 5.0) 3–5 d at 30–35°C
14061--47------N (3)
Yeasts and molds
APHA (food), AOAC, IFU. Beverages, wine, soft drinks, concentrates, Malt Extract (pH 4.5) 3–5 d at 20–25°C or at
fruit juice, foods, other products. 14086--47------N (6) 30–35°C depending on the
14086--47----CCN (8) target of the investigation
Yeasts and molds
APHA (food), AOAC, EP, USP. Pharmaceuticals, cosmetics, raw materials, Sabouraud (pH 5.6) < 5 d at 20–25°C
water (general quality), waste water, 14069--47------N (10)
other products.
Yeasts and molds
Wine, soft drinks, concentrates, sugar, Schaufus Pottinger | 2–5 d at 20–25°C or at
sugar products, other products. m Green yeast and mold 30–35°C depending on the
(pH 4.3) target of the investigation
14070--47------N (4)
14072--47------N (5)
14080--47------N (6)
14080--47----RDN
14083--47------N (3)
14091--47------N (8)
14091--47----RDN
Yeasts and molds and bacteria
ISO 7704. Beverages, beer, wine, soft drinks, Wallerstein | WL Nutrient 2–5 d at 30–35°C aerobic or
concentrates, fruit juice, other products. (pH 5.5) anaerobic depending on the
14089--47------N (2) target of the investigation
Yeasts and molds
VLB. Raw materials, beverages, beer, Wort (pH 4.4) 3–5 d at 20–25°C or at
wine, soft drinks, concentrates, foods, 14058--47------N (3) 30–35°C depending on the
30 other products. 14092--47----RDN (8) target of the investigation
Shelf Life Test Strains5) 1)
Reference Guide on page 34.
2)
A Set contains 100 Nutrient Pads and
100 membrane filters, both individually, sterile
24 06, 07, 09, 11, 21 packaged. The membrane filters are selected
for optimum growth together with the
corresponding nutrient media. The supplied
membrane filter type is listed within brackets:
(1) = green with dark green grid,
24 06, 07, 09, 11, 21 0.45 µm pore size
(2) = white with green grid, 0.45 µm pore size
(3) = gray (after wetting black) with white grid,
0.65 µm pore size
(4) = white with green grid, 0.65 µm pore size
(5) = white with green grid, 1.2 µm pore size
(6) = gray (after wetting black) with white grid,
24 07, 08, 09, 22, 26 0.8 µm pore size
(7) = white with black grid, 0.45 µm pore size
(8) = gray (after wetting black) with white grid,
0.45 µm pore size
(9) = white with green grid, 0.45 µm pore size,
High Flow (ideal for E. coli)
24 03, 09, 21, 25, 26 (10) = gray (after wetting black) with white grid,
0.45 µm pore size, High Flow
3)
Diameter of the membrane filter, 47 mm.
Order number for Nutrient Pad Sets
with 50 mm membrane filter as above, but
--47------N replaced by --50------N.
24 04, 09, 21, 22, 26, 30 Most of the NPS types are also available with
Microsart® e.motion Membrane Filters:
Order number as above, but ---N replaced by
-RDN.
Other NPS types and NPS with
24 07, 09, 21, 26, 27
Microsart® e.motion Membrane Filters on request.
4)
The incubation conditions are recommended
by Sartorius Stedim Biotech. They may be varied
according to the type of samples in compliance
with the reference standard or customer’s
requirements.
24 05, 20, 23, 24
5)
Test strains on page 32.

24 05, 20, 23, 24

24 01, 05, 20, 23, 24

24 03, 05, 20, 23, 24

24 05, 12, 19, 20, 23

24 05, 20, 23, 24

31
Detection Target and Reference 1) Test Sample Materials Media Type (pH) Recom.
Order No. (Filter Type)2), 3) Incubtion Conditions4)

Product-spoiling Microorganisms
Thermophilic spore formers and
mesophilic bacteria Fruit juice, sugar, sugar products, foods, Glucose Tryptone 18–72 h at 30–35°C for
APHA (dairy), APHA (food), AOAC, other products. (pH 6.8) mesophilic bacteria;
ICUMSA, IFU, ISO 7704, NCA. 14066--47------N (2) 48–72 h at 55 ±2°C for
thermophilic sporulating
microorganisms
Leuconostoc oenos and other wine
spoiling organ. Wine, fruit juice, other products. Jus de Tomate | 5–7 d at 30–35°C anaerobic
ISO 7704, Lanaridris& Lafon-Lafourcade. Tomato Juice (pH 5.0) (microaerophil); control
14079--47------N (1) for slowly growing micro-
organisms after 10 d is
recommended
Acid-tolerant microorganisms
APHA (water), IFU, ISO 7704, Raw materials, water (general quality), Orange Serum (pH 5.5) 3–5 d at 30–35°C aerobic or
MPP (packaging staff). waste water, wine, soft drinks, concentrates, 14062--47------N (1) anaerobic depending on the
fruit juice, foods, other products. 14062--47----RDN target of the investigation
Acid-tolerant microorganisms
APHA (water), IFU, ISO 7704, Raw materials, water (general quality), Orange Serum (pH 3.2) 3–5 d at 30–35°C aerobic or
MPP (packaging staff). waste water, wine, soft drinks, concentrates, 14096--47------N (6) anaerobic depending on the
fruit juice, foods, other products. 14096--47----RDN target of the investigation
Lactobacilli and Pediococci and
other beer spoiling organisms Beer, other products. VLB-S7-S (pH 5.5) 3–5 d at 30–35°C anaerobic
EBC, ISO 7704, MEBAC, VLB. 14059--47------N (2) (microaerophil)
Lactobacilli
APHA, ISO Fruit juice, beer, diary, foods, soft drinks, MRS (pH 6.1) 3–5 d at 30°C under anaerobic
other materials. 14077—47------N (1) conditions (microaerophil)
Mesophilic slime-forming bacteria
esp. Leu. Mesenteroides Soft drinks, concentrates, sugar, Weman (pH 5.5) 3–5 d at 30–35°C
ICUMSA, ISO 7704. sugar products, other products. 14065--47------N (1)

Test Strains [ATCC No.], [DSM No.]


01. Aspergillus brasiliensis 16404, 1988 17. Raw cane sugar solution (10%)
02. Bacillus cereus 11778, 345 18. Tap water
03. Bacillus subtilis subsp. spizizenii 6633, 347 19. Pediococcus damnosus 29358, 20331
04. Brevundimonas diminuta 19146, 1635 20. Penicillium commune 10428, 2211
05. Candida albicans 10231, 1386 21. Proteus mirabilis 29906, 4479
06. Enterobacter aerogenes 13048, 30053 22. Pseudomonas aeruginosa 9027, 1128
07. Enterococcus faecalis 29212, 2570 23. Rhodotorula mucilaginosa DSM 70403
08. Enterococcus faecium 19434, 20477 24. Saccharomyces cerevisiae 9763, 1333
09. Escherichia coli 8739, 1576 25. Salmonella enterica subsp. enterica
10. Geobacillus stearothermophilus serotype typhimurium 14028, 19587
7953, 5934 26. Staphylococcus aureus subsp. aureus
11. Klebsiella pneumoniae 13883, 30104 6538, 799
12. Lactobacillus lindneri DSM 20690 27. Staphylococcus epidermidis 12228, 1798
13. Lactobacillus plantarum subsp. plantarum 28. Escherichia coli 25922, 1103
14917, 20174 29. Lactobacillus brevis 14869, 20054
14. Leuconostoc mesenteroides subsp. 30. Pseudomonas aeruginosa 27853, 1117
mesenteroides 8293, 20343 31. Lactobacillus acetotolerans 43578, 20749
15. Oenococcus oeni 23279, 20252

32
Shelf Life Test Strains5) 1)
Reference Guide on page 34.
2)
A Set contains 100 Nutrient Pads and
100 membrane filters, both individually, sterile
packaged. The membrane filters are selected
for optimum growth together with the
24 02, 09, 10, 17, 26 corresponding nutrient media. The supplied
membrane filter type is listed within brackets:
(1) = green with dark green grid,
0.45 µm pore size
(2) = white with green grid, 0.45 µm pore size
(3) = gray (after wetting black) with white grid,
0.65 µm pore size
24 12, 14, 15, 24 (4) = white with green grid, 0.65 µm pore size
(5) = white with green grid, 1.2 µm pore size
(6) = gray (after wetting black) with white grid,
0.8 µm pore size
(7) = white with black grid, 0.45 µm pore size
(8) = gray (after wetting black) with white grid,
0.45 µm pore size
24 02, 05, 13, 14, 20, 23, 24 (9) = white with green grid, 0.45 µm pore size,
High Flow (ideal for E. coli)
(10) = gray (after wetting black) with white grid,
0.45 µm pore size, High Flow
24 02, 05, 13, 14, 20, 23, 24 3)
Diameter of the membrane filter, 47 mm.
Order number for Nutrient Pad Sets
with 50 mm membrane filter as above, but
--47------N replaced by --50------N.
24 06, 12, 13, 19, 24, 29 Most of the NPS types are also available with
Microsart® e.motion Membrane Filters:
Order number as above, but ---N replaced by
-RDN.
24 13, 19, 22, 29, 31
Other NPS types and NPS with
Microsart® e.motion Membrane Filters on request.

24 14 4)
The incubation conditions are recommended
by Sartorius Stedim Biotech. They may be varied
according to the type of samples in compliance
with the reference standard or customer’s
requirements.
5)
Test strains on page 32.

Remarks
The incubation conditions are recommended by Sartorius Stedim Biotech. They may be varied
according to the type of samples in compliance with the reference standard or customer‘s
requirements.
The description of the typical results or any pictures show typical appearance of the mentioned
microorganisms. In particular cases, color and shape of the colonies could vary from the expected
habitus. Further tests may be necessary to validate the result.
Sartorius Stedim Biotech shall not be liable for consequential and|or incidental damage sustained
by any customer from the use of its products.
Nutrient Pad Sets (NPS) are subject to continuous product improvement as part of our
product development program to align our products with changing application requirements.
For current specifications and lot release criteria please visit our homepage under:
www.sartorius-stedim.com/NPSSearch.

33
Reference Guide
The compositions of the pads are based on the recommendations of numerous different standards and regulations.

Abbreviation Title
AFNOR Association Franchaise de Normalisation
APHA (dairy) American Public Health Association: Standard Methods for the examination of dairy products
APHA (food) American Public Health Association: Compendium of methods for the microbiological examination of foods
APHA (water) American Public Health Association, American Water Works Association (AWWA) and Water Environment
Federation (WEF): Standard Methods for the Examination of Water and Waste Water
AOAC Association of Official Analytical Chemists
API American Petroleum Institute: Recommended practice for biological Analysis of Subsurface Injection waters
ASM American Society for Microbiology
BS British Standards
DAB Deutsches Arzneimittelbuch (German Pharmacopoeia, replaced by EP)
DIN 10110 Deutsches Institut für Normung: Mikrobiologische Fleisch­untersuchung. Bestimmung der E. coli.
(Microbial detection of E. coli on meat)
DIN 38411 Deutsches Institut für Normung: Deutsche Einheitsverfahren zur Wasser-, Abwasser- und Schlamm­
untersuchung (German standard for water, waste water and sludge analysis)
DGHM Deutsche Gesellschaft für Hygiene und Mikrobiologie (German Association of Hygiene and Microbiology)
EBC European Brewery Convention
EG 98/83 European Guideline 98/83: Water Quality for human purpose
EP European Pharmacopoeia
EPA U.S. Environmental Protection Agency: Laboratory standards for equipment and materials
FDA U.S. Federal Drug Administration
HMSO Her Majesty’s Stationery Office: Department of Health and Social Security (1982) “The Bacteriological
Examination of Drinking Water Supplies”. Report 71, HMSO, London
ICUMSA International Commission for Uniform Methods of Sugar Analysis
IDF International Dairy Federation
IFU International Federation of Fruit Juice Producers
ISO 6222 International Organization for Standardization: Water Quality - Enumeration of culturable micro-organisms
ISO 6579-1981 International Organization for Standardization: Microbiology. General guidance on methods for the
detection of Salmonella. Reference method
ISO 7704 International Organization for Standardization:
Water Quality, Evaluation of membrane filters used for microbiological analysis
ISO 7899-2 International Organization for Standardization:
Water Quality – Detection and enumeration of intestinal enterococci
ISO 8199 International Organization for Standardization:
Water Quality – General Guide to the enumeration of micro-organisms by culture
ISO 9308-1 International Organization for Standardization:
Water Quality – Detection and enumeration of E. coli and coliform bacteria
EN ISO 16266 European|International Organization for Standardization:
Water Quality – Detection and enumeration of Ps. aeruginosa
JFoodP Journal of Food Protection
JIBrew The Journal of the Institute of Brewing
LLL Method described by Lanaridris& Lafon-Lafourcade
LMBG Amtliche Sammlung von Untersuchungsverfahren nach dem §35 des Lebensmittel- und Bedarfs­
gegenständegesetzes des BGA (testing procedures for food stuffs and articles of daily use)

34
Abbreviation Title
MEBAK Methodensammlung der Mitteleuropäischen Brauereitechnischen Analysenkommission
(methods of the Central European brewery commission)
MNO Verordnung über natürliches Mineralwasser, Quellwasser und Tafelwasser (Mineral/Table Water Guideline)
MPP Merkblätter für die Prüfung von Packmitteln (Testing procedures for packaging stuff)
NCA National Canners Association: A Laboratory manual of the canning industry
USDA U.S. Department of Agriculture
USP United States Pharmacopoeia
VLB Versuchs- und Lehranstalt für Brauerei in Berlin (institute of brewery)
ZenHyg Zentralblatt für Hygiene (Journal of Hygiene)

DIN standards and the „Amtliche Sammlung von Untersuchungsverfahren nach dem
§ 35 des Lebensmittel- und Bedarfsgegenständegesetzes des BGA“ are available through the German
publisher Beuth-Verlag, Burggrafenstr. 6, 10787 Berlin

35
Sales and Service Contacts
For further contacts, visit www.sartorius.com

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