Further Reading
Franta R and Beck B (1986) Alternatives to cane and beet
sugar. Food Technology 40: 116–128.
Kretchmer N and Hollenbeck CB (1991) Sugars and Sweet-
eners. Boca Raton: CRC Press.
Lawrence JF and Charbonneau CF (1988) Determination of
seven artificial sweeteners in diet food preparations by
reverse-phase liquid chromatography with absorbance
detection. Journal of the Association of Official
Analytical Chemists 71: 934–937.
O’Brien-Nabors L and Gelardi RC (1991) Alternative
Sweeteners. New York: M. Dekker.
ACIDOPHILUS
MILK
W Kneifel and C Bonaparte, University of
Agricultural Sciences, Vienna, Austria
Copyright 2003, Elsevier Science Ltd. All Rights Reserved.
Background and History
0001 Since the first documentation of the beneficial role
of Lactobacillus acidophilus in correcting disorders
of the human digestive tract in 1922, products con-
taining L. acidophilus, especially various types of
Acidophilus milk, have become increasingly popular.
Today, a multitude of such products are commercially
available, many of them being assigned to the category
of probiotic foods. Most of these probiotics possess a
bacterial microflora of well-documented and scienti-
fically proven bacterial strains with several benefical
properties. Besides other categories of foods contain-
ing special ingredients, these products have also
recently been subclassified under the umbrella of
functional foods.
0002 In general, the human body is inhabitated by more
than 500 different bacterial species; among them,
the lactobacilli play an important ecological role.
Besides their important gut-associated function, lacto-
bacilli are also part of various other human-specific
microbial ecosystems, e.g., skin, vagina, mouth, nasal,
and conjunctival secretions. L. acidophilus is the best
known of the health-promoting lactobacilli of
mammals and a naturally resident species of the
human gastrointestinal tract. It colonizes segments of
the lower small intestine and parts of the large intes-
tine, together with other lactobacilli species, such
as L. salivarius, L. leichmanii, and L. fermentum.It
is interesting to note that these resident Lactobacillus
species should be distinguished from the spectrum of
so-called transient Lactobacillus species, which are
represented by L. casei.
0003 Historically, in 1900, Australian researchers isol-
ated L. acidophilus from fecal samples of bottle-fed
infants for the first time and named it ‘Bacillus acid-
ophilus.’ The actual nomenclature L. acidophilus is
derived from acido (acid) and philus (loving) and this
designation reflects the acidotolerant potential of this
species. In 1959, Rogosa and Sharpe presented a
detailed description of this bacterium.
Fundamental Characteristics of
Lactobacillus acidophilus
0004Together with 43 other species, L. acidophilus is
listed as a member of the genus Lactobacillus which
belongs to the heterogeneous category of lactic acid
bacteria. Lactobacilli are Gram-positive, nonmotile,
catalase-negative, nonspore-forming rods with vary-
ing shapes, ranging from slender, long rods to cocco-
bacillary forms. They are considered as (facultative)
anaerobes with microaerophilic properties. L. acido-
philus usually appears as rods with rounded ends,
with a size of 0.6–0.9 1.5–6 mm, mainly organized
singly or in pairs or short chains (Figure 1). The cell
wall peptidoglycan is of the Lys-d-Asp type; the mean
proportion of guanine and cytosine in the DNA
ranges between 34 and 37%. With rare exceptions,
this bacterium shows good growth at 45
C but not
below 15
C, having an optimum growth temperature
in the range of 35–38
C. Substrates with pH values
of 5.5–6.0 are preferred. Metabolically, it is a typical
obligately homofermentative bacterium and produces
racemic lactic acid (both the lþ and the d enantio-
meric forms) from lactose, glucose, maltose, sucrose,
and other carbohydrates. Usually, it follows the
Embden–Meyerhof–Parnas pathway for glucose
metabolism. Important growth factor requirements
are acetic or mevalonic acid, riboflavin, pantothenic
acid, niacin, folic acid and calcium, but not cobala-
min, pyridoxine, and thymidine. Starch and cello-
biose are fermented by most strains. Another
differential key criterion for the distinction from
other lactobacilli (e.g., L. delbrueckii subsp. bulgar-
icus) is its capability of cleaving esculin. Further
differential criteria are the utilization of trehalose,
melibiose, raffinose, ribose, and lactose. While
ACIDOPHILUS
MILK 3