Microbial cells are structurally complex and carry out numerous functions. Nutrients are required for microbial growth to support biosynthesis and energy release. Microorganisms use nutrients and a source of energy to construct new cellular components and do cellular work.
Common
Nutrient Requirements
Macroelements/Macronutrients : Macro elements or
macronutrients are required by microorganisms in relatively large
amounts. Over 95% of microbial cell dry weight is made up of a few major
elements: carbon, oxygen, hydrogen, nitrogen, sulfur, phosphorus, potassium,
calcium, magnesium, and iron, these are the Macroelements/Macronutrients. Carbon,
oxygen, hydrogen, nitrogen, sulfur, phosphorus- C, O, H, N, S, and P-
are components of carbohydrates, lipids, proteins, and nucleic acids.
Potassium, calcium, magnesium, and
iron exist in the cell as cations and play a variety of roles. Potassium (K+)
is required for activity by a number of enzymes, including some of those
involved in protein synthesis. Calcium (Ca2+), contributes to
the heat resistance of bacterial endospores among other functions. Magnesium (Mg2+)
serves as a cofactor for many enzymes, complexes with ATP, and stabilizes
ribosomes and cell membranes. Iron (Fe2+and Fe3+)
is a part of cytochromes and a cofactor for enzymes and electron-carrying
proteins.
Micronutrients
or trace elements :
Micronutrients or trace elements are required in small amounts for all
microorganisms, in addition to macroelements. These include manganese, zinc,
cobalt, molybdenum, nickel, and copper and are needed by most cells. These
are required in such small amounts that they are available as contaminants from
water, glassware, and regular media components. Often these are adequate for
growth.
In nature, micronutrients are
ubiquitous and probably do not usually limit growth.
Micronutrients are normally a part
of enzymes and cofactors,
and they aid in the catalysis of reactions and maintenance of protein
structure. For example, zinc (Zn2+) is present at the active
site of some enzymes but can also be involved in the association of regulatory
and catalytic subunits. (e.g., E. coli aspartate carbamoyl
transferase). Manganese (Mn2+) aids many enzymes that
catalyze the transfer of phosphate groups. Molybdenum (Mo2+)
is required for nitrogen fixation, and cobalt (Co2+) is a
component of vitamin B12.
Microorganisms
may have particular requirements according to the environment or as part of
their morphology. For example, bacteria/ archaea growing in saline lakes and
oceans require high concentrations of sodium ion (Na+). Diatoms need
silicic acid (H4SiO4) to construct their beautiful cell
walls of silica [(SiO2)n].
In general, microorganisms require
a balanced mixture of nutrients. If an essential nutrient is in short supply,
microbial growth will be limited regardless of the concentrations of other
nutrients.
Requirements
For Carbon, Hydrogen, Oxygen, And Electrons
All organisms need carbon,
hydrogen, oxygen, and a source of electrons. Carbon is needed
for the skeletons or backbones of all the organic molecules which make the organisms. Hydrogen
and oxygen are also important elements found in organic
molecules. Electrons are needed for electron transport chain
and for other oxidation-reduction reactions which can provide energy for use in
cellular work. Electrons are also needed to reduce molecules during
biosynthesis (e.g., the reduction of CO2 to form organic
molecules).
Molecules serving as carbon sources
also provide hydrogen and oxygen. Thus,
the requirements for carbon, hydrogen, and oxygen are satisfied together. However,
one carbon source, carbon dioxide (CO2), supplies only
carbon and oxygen because CO2 is the most oxidized form of
carbon, lacks hydrogen, and is unable to donate electrons during
oxidation-reduction reactions. So it cannot be used as a source of hydrogen,
electrons, or energy.
Organisms that use CO2 as
their sole or principal source of carbon are called autotrophs.
Because CO2 cannot supply their energy needs, they must obtain
energy from other sources, such as light or reduced inorganic molecules.
Heterotrophs are organisms that use reduced,
preformed organic molecules as their carbon source. They can also obtain
hydrogen, oxygen, and electrons from the same molecules. Thus, organic carbon
sources also provide electrons to be used in electron transport as well as in
other oxidation-reduction reactions, so heterotrophs use their carbon source as
an energy source also.
The more reduced the organic carbon
source (i.e., the more electrons it carries), the higher its energy content.
Thus, lipids have a higher energy content than carbohydrates.
Heterotrophic microorganisms can
use many carbon sources. There is no naturally occurring organic molecule that
cannot be used by some microorganism. Actinomycetes, common soil
bacteria, will degrade amyl alcohol, paraffin, and even rubber. Some bacteria
can use almost anything as a carbon source; for example, Burkholderia
cepacia can use over 100 different carbon compounds. Microbes can
degrade even relatively indigestible human-made substances such as pesticides.
This is usually carried out by complex microbial communities (microbial
consortia). These molecules sometimes are degraded in the presence of a
growth-promoting nutrient that is metabolized at the same time—a process
called cometabolism. Other microorganisms can use the products
of this breakdown process as nutrients.
But some microbes are extremely
fastidious and catabolize only a few carbon compounds. Cultures of methylotrophic bacteria
metabolize methane, methanol, carbon monoxide, formic acid, and related
one-carbon molecules. Parasitic members of the genus Leptospira use
only long-chain fatty acids as their major source of carbon and energy.
Requirements
For Nitrogen, Phosphorus, And Sulfur
Microorganisms require large
quantities of nitrogen, phosphorus, and sulfur for growth. These elements may
be acquired from the same nutrients/organic sources that supply carbon, or from
other inorganic sources.
Nitrogen is needed for the synthesis
of amino acids, purines, pyrimidines, some carbohydrates and lipids, enzyme
cofactors, and other substances. Many microorganisms can use the nitrogen
obtained in amino acids (organic source). Others incorporate ammonia directly through the action
of enzymes such as glutamate dehydrogenase or glutamine synthetase and
glutamate synthase. Most phototrophs and many chemotrophic microorganisms
reduce nitrate to ammonia and incorporate the ammonia in a process known
as assimilatory nitrate reduction (inorganic sources) A variety of bacteria (e.g.,
many cyanobacteria and the symbiotic bacterium Rhizobium) can assimilate
atmospheric nitrogen (N2) by reducing it to ammonium (NH4).
This is called nitrogen fixation.
Phosphorus is present in nucleic acids,
phospholipids, nucleotides like ATP, several cofactors, some proteins, and
other cell components. Almost all microorganisms use inorganic phosphate as
their phosphorus source and incorporate it directly. Low phosphate levels can
limit microbial growth in many aquatic environments. Some microbes, such
as Escherichia coli, can use both organic and inorganic phosphate.
Some organophosphates such as hexose 6-phosphates can be taken up directly by
the cell. Other organophosphates are hydrolyzed in the periplasm by the enzyme
alkaline phosphatase to produce inorganic phosphate, which then is transported
across the plasma membrane.
Sulfur is needed for the synthesis of substances like the amino acids cysteine and methionine, and some carbohydrates, biotin, and thiamine. Most microorganisms use sulfate (inorganic source) as a source of sulfur and reduce it by assimilatory sulfate reduction. A few microorganisms require a reduced form of sulfur such as cysteine (organic source).
Growth
Factors
Some microorganisms have the
enzymes and biochemical pathways needed to synthesize all cell components using
minerals and sources of energy, carbon, nitrogen, phosphorus, and sulfur. Some
lack one or more of the enzymes needed to manufacture some indispensable
constituents. So, they must obtain these constituents or their precursors from
the environment. Organic compounds that are essential cell components
or precursors of such components but cannot be synthesized by the organism are
called growth factors. There are three major classes of growth factors:
(1)
amino acids, (2) purines and pyrimidines, and (3) vitamins.
Amino
acids are
needed for protein synthesis; purines and pyrimidines for
nucleic acid synthesis. Vitamins are small organic molecules
that usually make up all or part of enzyme cofactors and are needed in only
very small amounts to sustain growth.
Functions of Some Common Vitamins in Microorganisms |
||
Vitamin |
Functions |
Microorganisms
Requiring Vitamin |
Biotin |
Carboxylation (CO2 fixation) One-carbon
metabolism |
Leuconostoc mesenteroides Saccharomyces cerevisiae |
Cyanocobalamin
(B12) |
Molecular
rearrangements |
Lactobacillus spp. |
Folic
acid |
One-carbon
metabolism |
Enterococcus faecalis |
Pyridoxine
(B6) |
Amino
acid metabolism (e.g., transamination) |
Lactobacillus spp. |
Niacin
(nicotinic acid) |
Precursor
of NAD and NADP |
Haemophilus
influenzae |
Riboflavin
(B2) |
Precursor
of FAD and FMN |
Dictyostelium spp |
Some
microorganisms require many vitamins; for example, Enterococcus
faecalis needs eight different vitamins for growth.
Other
growth factors required are; heme (from hemoglobin or
cytochromes) is required by Haemophilus influenzae, and some
mycoplasmas need cholesterol.
Understanding
the growth factor requirements of microbes has significant practical
applications. Microbes with known, specific requirements and those that
produce large quantities of a substance (e.g., vitamins) are useful.
Microbes
with a specific growth factor requirement can be used in bioassays for
the factor they need. A typical assay is a growth-response assay,
which allows the amount of growth factor in a solution to be determined. The
amount of growth in a culture is related to the amount of growth factor
present. Ideally, the amount of growth is directly proportional to the amount
of growth factor; if the growth factor concentration doubles the amount of
microbial growth doubles.
For
example, Lactobacillus and Streptococcus can
be used in microbiological assays of most vitamins and amino acids.
Microbiological assays are specific, sensitive, and simple. They still are used
in the assay of substances like vitamin B12 and biotin, despite
advances in chemical assay techniques.
Microorganisms
which are able to synthesize large quantities of vitamins can
be used to manufacture these compounds for human use. Several water-soluble and
fat-soluble vitamins are produced partly or completely using industrial
fermentations. Good examples of such vitamins and the microorganisms that
synthesize them are
· riboflavin
(Clostridium, Candida, Ashbya, Eremothecium)
· coenzyme
A (Brevibacterium)
· vitamin
B12 (Streptomyces, Propionibacterium, Pseudomonas)
· vitamin
C (Gluconobacter, Erwinia, Corynebacterium)
· carotene
(Dunaliella)
· vitamin
D (Saccharomyces).
Research
focuses on improving yields and finding microorganisms that can produce large
quantities of other vitamins.
Nutritional
Types of Microorganisms
Depending on how the need for carbon, energy, and electrons is fulfilled microorganisms can be classified.
With respect to their preferred source of carbon, there are heterotrophs or autotrophs.
There are only two sources of energy available to organisms: Phototrophs use
light as their energy source; chemotrophs obtain energy from
the oxidation of chemical compounds (either organic or inorganic).
Microorganisms also have only two sources of electrons. There are Lithotrophs (i.e.,
“rock-eaters”) which use reduced inorganic substances as their electron source,
and organotrophs which obtain electrons from reduced organic
compounds.
Sources of Carbon, Energy, and
Electrons |
||
Carbon Sources |
||
Autotrophs |
CO2 sole
or principal biosynthetic carbon source |
|
Heterotrophs |
Reduced,
preformed, organic molecules from other organisms |
|
Energy Sources |
||
Phototrophs |
Light |
|
Chemotrophs |
Oxidation
of organic or inorganic compounds |
|
Electron Sources |
||
Lithotrophs |
Reduced
inorganic molecules |
|
Organotrophs |
Organic
molecules |
|
In
spite of the great metabolic diversity seen in microorganisms, most can be
placed in one of five nutritional classes based on their primary sources of
carbon, energy, and electrons.
Major Nutritional Types of
Microorganisms |
||||
Nutritional Type |
Carbon Source |
Energy Source |
Electron Source |
Representative Microorganisms |
Photolithoautotrophy (photolithotrophic
autotrophy) |
CO2 |
Light |
Inorganic
e- donor |
Purple
and green sulfur bacteria, cyanobacteria |
Photoorganoheterotrophy (photoorganotrophic heterotrophy) |
Organic
carbon but CO2 may also be used |
Light |
Organic
e- donor |
Purple
nonsulfur bacteria, green nonsulfur bacteria |
Chemolithoautotrophy (chemolithotrophic
autotrophy) |
CO2 |
Inorganic
chemicals |
Inorganic
e- donor |
Sulfur-oxidizing
bacteria, hydrogen-oxidizing bacteria, methanogens, nitrifying bacteria,
iron-oxidizing bacteria |
Chemolithoheterotrophy/
mixotrophy (chemolithotrophic heterotrophy) |
Organic
carbon, but CO2 also used |
Inorganic
chemicals |
Inorganic
e-donor |
Some
sulfur-oxidizing bacteria (e.g., Beggiatoa) |
Chemoorganoheterotrophy
(chemoorganotrophic heterotrophy) |
Organic
carbon |
Organic
chemicals often same as C source |
Organic
e-donor often same as C source |
Most
non photosynthetic microbes, including most pathogens,
fungi, many protists,
and many archaea |
The
majority of microorganisms are either photolithotrophic autotrophs or
chemoorganotrophic heterotrophs.
Photolithotrophic
autotrophs (often
called photoautotrophs or photolithoautotrophs) use light energy and have CO2 as
their carbon source. Photosynthetic protists and cyanobacteria use water as the
electron donor and release oxygen. Other photolithoautotrophs, such as the
purple and green sulfur bacteria, cannot oxidize water but get electrons from
inorganic donors like hydrogen, hydrogen sulfide, and elemental sulphur.
Chemoorganotrophic
heterotrophs (often
called heterotrophs or chemoheterotrophs, or chemoorganoheterotrophs) use
organic compounds as sources of energy, hydrogen, electrons, and carbon.
Usually, the same organic nutrient will satisfy all these requirements. All
pathogenic microorganisms are chemoheterotrophs.
The other nutritional classes are
very important ecologically though they have only fewer known microorganisms.
Some photosynthetic bacteria (purple and green bacteria) use organic matter as
their electron donor and carbon source. These photoorganotrophic
heterotrophs (photoorganoheterotrophs) are common in polluted lakes
and streams. Some of these bacteria also can grow as photoautotrophs with
molecular hydrogen as an electron donor.
Chemolithotrophic
autotrophs (chemolithoautotrophs),
oxidize reduced inorganic compounds such as iron, nitrogen, or sulfur molecules
to derive both energy and electrons for biosynthesis. Carbon dioxide is the
carbon source.
Chemolithoheterotrophs, also known as mixotrophs, use
reduced inorganic molecules as their energy and electron source, but derive
their carbon from organic sources. Chemolithotrophs contribute greatly to the
chemical transformations of elements (e.g., the conversion of ammonia to
nitrate or sulfur to sulfate) that continually occur in ecosystems.
For example, many purple nonsulfur
bacteria act as photoorganotrophic heterotrophs in the absence of oxygen but
oxidize organic molecules and function chemoorganotrophically at normal oxygen
levels. When oxygen is low, photosynthesis and chemoorganotrophic metabolism
may function simultaneously. This sort of flexibility seems complex and
confusing, but it gives these microbes an advantage if environmental conditions
frequently change.
Conclusion
Microorganisms
require about 10 elements in large quantities for the synthesis of
macromolecules. Several other elements are needed in very small amounts and are
parts of enzymes and cofactors.
All
microorganisms can be placed in one of a few nutritional categories on the
basis of their requirements for carbon, energy, and electrons.