Protein Banding Pattern and Major Amino Acid Component in De-Oiled Pupal Powder of Silkworm, Bombyx mori Linn.
S. Nirmal Kumar,
C. Anil Kumar Bhat
Quantitatively Bombyx mori pupal powder contains significantly higher amount of protein in female as compared to male in both the hybrids of PM x CSR2 and CSR2 x CSR4 studied. On an average, in the former hybrid 14.81% and in the later hybrid 14.58% soluble protein was present as compared to total protein 60.81 and 63.66%, respectively. Qualitatively, no difference was found in amino acid content between the male and female of both hybrids. Five major amino acids found in PM x CSR2 were nor leucine, methionine, glutamic acid, hydroxyl proline, Aspartic acid and in CSR2 x CSR4 were isoleucine, valine, amino butyric acid, hydroxyl proline and leucine. SDS PAGE results reveled that there was no polymorphism between the sexes of two hybrids. Two polypeptides were identified in the range at 43 and 14.3 KD. Of the two polypeptides identified, the banding pattern of 43 KD was prominent in both the sexes of the two hybrids.
The Silkworm, Bombyx mori L. is an economically important insect, which
produces large quantity of silk. In silk reeling process, large quantity of
waste accumulates in the form of pupae and left over unreelable silk, which
could be utilized in a better way by producing value added products with the
adoption of improved technology. By this, the cost of production of silk can
be reduced either by standardization of processing methods or by utilizing the
waste produced by the silk industry (Majumder, 1992). By-products of an industry
are often brought to purposeful utilization to augment the profits (Sahay et
al., 1997). This vital aspect so far seems to have not been taken proper
care in sericulture industry. It is a well-known fact that pupae, which are
obtained after reeling of silkworm cocoons are generally thrown away which is
very rich in protein, oil, carbohydrate and minerals. The pupa, which is available
abundantly in the reeling industry as a waste, can be utilized as a high potential
raw material for various industries including pharmaceuticals. The oil extracted
from the pupa is used in paints, varnishes soaps, candles, pharmaceuticals,
bio-diesel and plastic industries (Basavanna et al., 1967; Datta et
al., 1993; Chavan et al., 1999; Chaudhury, 2003). Sarker and Quader
(1990) have studied extractability and properties of pupal oil. Pupal powder
is generally used as feed for fowl, fish and swine as it is rich in protein
(Nagaraj and Basavanna, 1969; Shiva Prakash, 1988; Mathur et al., 1988;
Saratchandra, 1988; Bose et al., 1993). In fact the protein of pupae
is better than the protein of soyabean, fish or beef. Silkworm pupae is a nutritious
food for human diet as it contains a balanced amount of moisture, chitin, water
soluble proteins, carbohydrates, amino acids and vitamin C besides crude protein
as the major constituent (Majumder, 1992; Majumder et al., 1994; Ashok
Kumar et al., 2000). Pupae protein has a well-balanced amino acid composition.
Silkworm meal made of silkworm/pupa has been used in feeding monogastric and
ruminant species for many years in Asian countries (Lakshminarayana and Thirumalarao,
1971; Majumder et al., 1994; Roychoudhury and Joshi, 1995). The protein
is one of the important macromolecule found in all living cells, which is nothing
but polymer of different amino acids. There are about 20 amino acids, which
make these proteins. These amino acids are organic, amphoteric molecules having
an amino group at one end and a carboxylic group at the other end. It was thought
worthwhile to obtain few byproducts from the pupae and find out the economic
utilization of these by-products for commercial exploitation. Therefore, the
present investigation was taken up to study the protein, amino acid contents
and protein quality in the de-oiled pupal powder of commercially available hybrids.
MATERIALS AND METHODS
Two hybrids viz., PM x CSR2 (multivoltine x bivoltine) and CSR2xCSR4 (bivoltine x bivoltine) were reared following standard procedure of Rajan and Himantharaj (2005). Both male and female pupae were separated and weighed separately. The fresh pupae were dried in hot air drier at 50°C for 4 days. The dried pupae were ground in mortar and pestle. Oil was removed by solvent soxhlet extraction process using chloroform: methanol = 2:1 (v/v) (Shreekantaswamy and Siddalingaiah, 1980). Total protein (Lowry et al., 1951) and total nitrogen content (Kjeldhal method) (Wilson and Walker, 2000) of the de-oiled pupal powder were estimated.
To analyze the banding pattern of de-oiled pupal powder, the standard procedure
for SDS Polyacrylamide gel of Laemmli (1970) was followed. In the present study
10% separating and 4% stacking gel was used. The samples were taken out of -80°C
and allowed to thaw on ice. Five gram of de-oiled protein powder was dissolved
in tris buffer of pH 7. The grounded mixture was centrifuged for 15 min at 8000
rpm. The supernatant was used for further analysis of protein. The samples were
mixed with PBS (Phosphate buffer solution) and sample buffer, boiled for 4 min
at 96°C. The protein marker of 3.5-205 KD was used as standard (GENEI Industries,
Inc., Saginaw, MI 48601).
Thin Layer Chromatography
All standard amino acid samples (Amino acid reference collection kit, S.D.
Fine Chem. Ltd., India) were dissolved in citrate buffer and water (100 μg
mL-1) depending upon their solubility. Four gram of de-oiled pupal
power was added to 50 mL of 6N HCl and kept in an oven at 75-80°C for 12
h or 36-40°C for 36 h to hydrolyze the pupal protein. The hydrolyzed samples
were centrifuged at 10,000 rpm for 15 min, filtered through Whatman No. 1 filter
paper and the residue was mixed with known amount of water, centrifuged again
at 10,000 rpm. This procedure was repeated for 3-4 times until supernatant gives
negative Ninhydrin test. All the supernatants were collected and concentrated
to remove HCl. The absence of HCl solution in the supernatant was confirmed
by pH paper test. Later 4 g of activated charcoal powder was added to each sample
to remove undesired colour and the sample was kept in refrigerator for over
night and filtered. The process was repeated to obtain the colourless solution.
Amino acids extracted from silkworm pupae are in yellowish powder form. Standard
TLC procedure was followed (Palanivelu, 2004) to identify the major amino acid
content. Sample and standard were run on the plates coated with silica G and
mobile phase used was n butyl alcohol, acetic acid and water in the ratio of
8:2:2. After developing, plates were sprayed with 0.3% ninhydrin solution and
retention factor (Rf) values were calculated.
RESULTS AND DISCUSSION
Estimation of Oil, Crude-Protein and Others
23.6 and 37.8 g de-oiled pupal powder each was obtained from 100 g fresh
male and female pupae in PM x CSR2 whereas 21.5 and 36.5 g in male and female
pupae in CSR2 x CSR4 (Table 1). Statistical analysis (CD at
5%) showed there is significant difference in de-oiled pupa powder recovery
between the male and female pupae of both the hybrids. Female pupae yielded
more pupa powder than male in both the hybrids. Similarly oil and crude protein
with other constituents were estimated as 40.02 and 59.98% in male pupae and
25.17 and 74.67% in female pupae of PM x CSR2, whereas in CSR2 x CSR4 these
were 40.00 and 60.00% in male and 24.0 and 76.00% in female, respectively. It
was found that in pupa powder oil is more in male than female of both the hybrids,
whereas, crude protein was significantly more in female of both the hybrids
as compared to male. Choudhury and Kumar (1979) reported that Antheraea mylitta
pupae contain 20-25% oil. The oil content in Eri Silkworm pupae was estimated
to be in the range of 18-20% (dry basis) by Shanker et al. (2006). Mishra
et al. (2003) found the proximate composition (%) of total protein ranges
between 12 to 16%, total fat between 11 to 20%, carbohydrate between 1.2 to
1.8%, moisture between 65 to 70% and ash between 0.8 to 1.4% for non-mulberry
and mulberry silkworm pupae.
Quantification of Protein
The results of the present study showed 9.08% nitrogen in male pupa and
10.38% in female pupa of PM x CSR2. Similarly, 9.85% nitrogen in male pupa and
10.52 % in female pupa of CSR2 x CSR4. In practice the nitrogen content of protein
is generally assumed to be 16% by weight (Wilson and Walker, 2000). Therefore,
for calculating protein percentage in tissue, nitrogen content is multiplied
by the factor 6.25. It revealed that the pupae are rich source of protein. Average
protein content in PM x CSR2 pupae is 60.80%. It was observed that male pupa
contain 56.75% whereas female pupae contain 64.88% of total protein. Similarly
the average protein content in CSR2 x CSR4 pupa is 63.66 %. The male pupae contain
61.56% and female pupae contain 65.76% of total protein (Table
The biochemical analysis by Lowrys method also revealed that PM x CSR2 male
pupae contained 141.6 mg g-1 and female pupae contain 154.60 mg g-1
of soluble protein (average 148.1 mg g-1). Similarly in CSR2 x CSR4,
male pupae contain 125.10 mg g-1 and female pupa contain 166.47 mg
g-1 of soluble protein (average 145.78 mg g-1).
of oil (%) and crude-protein and others in the pupae of two hybrids CSR2
x CSR4 and PM x CSR2
nitrogen and protein by Kjeldhal method in silkworm pupae, Bombyx mori
Significant at 1% level
Data reveled that female pupae contains significantly higher amount of soluble
protein compared to male pupae in both the hybrids (Table 2).
Comparing the results, it is noted that, on an average 14.81 and 14.58% soluble
protein was present in PM xanalysis is a Precise method for the determination
of total nitrogen contains in the sample such as DNA, uric acid, enzymes and
all the NO2 and NO3 etc. By Kjeldhal method, total protein
present in the sample can be estimated through factor multiplication, Whereas
by Lowry method, only soluble protein digested through 10% TCA can be determined.
Other proteins insoluble in TCA could not be measured. Accordingly, there is
difference in total protein content and soluble protein content. The result
showed that female pupae contains significantly higher amount of protein as
compared to male of both the hybrids. According to Rao (1994), spent silkworm
pupae were analyzed for its nutrient composition and their protein quality was
evaluated in weanling rats. Protein content of the pupae was found to be 48.7%.
Defatted spent silkworm pupae meal contained 75.2% protein, which perhaps may
be based on total nitrogen estimation. The pupae of Antheraea mylitta
which contains 80% protein can be suitably utilized in baking industry for manufacturing
protein rich biscuits (Agarwal et al., 1974). Bose and Majumder (1990)
reported that the pupae powder contains 7.18, 29.57% fat, 48.98% protein (Kjeldhal
method), 4.655% glycogen, 3.37% chitin, 2.19% ash and 3.7% vitamins etc. which
shows that pupa is good source of protein and fat.
Each protein is unique and characterized by its amino acid composition and
sequence. In any protein, many amino acids (usually more than hundred) are linked
by peptide bonds to form polypeptide chain. The cleavage of peptide bonds is
usually achieved by boiling the protein in 6N HCl, which hydrolyzes peptide
bonds thereby releasing free amino acids. So in order to determine amino acid
composition of a protein, it is necessary to break down the polypeptide chain
into its constituent amino acids by hydrolysis (Geis, 1989). It was found that
the nutritionally important amino acids were present in silkworm pupa of both
the hybrids (PM x CSR2 and CSR2 x CSR4). Both essential and non-essential amino
acids were identified by comparing their Rf values with standard amino acids.
It was found that both male and female pupae of CSR2 x CSR4 contain five amino
acids viz., nor leucine, methionine, glutamic acid, hydroxyl proline and aspartic
acid. Whereas, in the pupae of both the sexes of PM x CSR2 contain iso-leucine,
valine amino butyric acid, hydroxyl proline and leucine. There is no difference
in amino acid content between the two sexes of the same hybrid whereas there
is difference in amino acid content between the hybrids. Hydrolyzed pupae of
silkworm were analyzed for amino acid content by Majumder et al. (1994)
and found to contain lysine, leucine + isoleucine, valine + methionine, threonine,
cystine, tyrosine, histidine, arginine, glutamic acid, glycine, serine, alanine,
proline and cysteic acid. Amino acids extracted from silkworm pupa are in yellowish
powder form. It is soluble in water with pH between 4 to 6.5 and positive to
ninhydrin reaction. In the present study pupae hydrolysate contains all essential
amino acids of group 1 (isoleucine, leucine, methionine and valine), group 2
(aspartic acid and glutamic acid) and semi essential amino acids (proline-could
be produced in body) that are important for human beings and are getting only
through food. These amino acids are necessary for human health. As per the quality
standards of FAO/WHO, the nutritive value of silkworm pupae is superior to that
of eggs and milk (Xiao, 1983). Its good solubility in water enables to produce
transparent beverage. It has been widely used in health food industry, such
as amino acid drink, granule, capsule, fruity beverage and kinds of good additives.
It can also be used as raw material for the production of medicinal amino acids
and single amino acid (http://www.alibaba.com/showroom/Amino_Acid_Powder.html).
Methionine is the most important amino acid for the catalysis of the biotin
enzyme (Shenoy et al., 1992), gamma-aminobutyric acid and glutamate which
are neurotransmitters (Dodd et al., 1992). Rao (1994) reported that
the essential amino acid content of the pupal protein was similar to that of
whole egg protein with the exception of tryptophan (0.9 16 g of N).
banding pattern of de-oiled pupae powder of silkworm Bombyx mori.
1. Maker, 2. PM x CSR2 ♂♂, 3. PM x CSR2 ♀♀, 4.
CSR2 x CSR4 ♂♂, 5. CSR2 x CSR4 ♀♀ and 6. No sample
Tryptophan is the limiting amino acid of pupal protein. The chemical score
of the protein was found to be 60, as compared to 100 for whole egg protein.
The protein-banding pattern studied on SDS PAGE electrophoresis (Fig. 1) indicated that there was no difference in banding pattern of polypeptide between male and female de-oiled pupal protein. Thus the present study indicated the quantitative difference in pupal protein between the two sexes, which may help in identifying the functional significance of these proteins. Two bands were identified in the range of 43 and 14.3 KD. Of the two bands, the band with molecular weight of 43 KD was prominent in both the sexes. The electrophoretic separation of pupal proteins shows two prominent bands of similar molecular weight in male and female pupa of PM x CSR2 and CSR2 x CSR4. However, a significant band at 43 KD was more prominent in the female pupa suggesting that the quantity of this particular protein is relatively high. However, the electrophoretic separation of non-mulberry Eri silkworm pupal proteins showed six prominent bands of similar molecular weight in male and female and there was no difference in banding pattern between male and female. In both sexes six bright bands were observed in the range at 66, 45, 34, 24, 18 and 14.3 KD (Reddy et al., 2004), whereas, only two bands obtained in the present study may be due to the difference in species.
In brief, female pupae yielded more pupa powder than male in both the hybrids. Oil content was more in male pupae compared to female pupae, whereas the quantity of crude and soluble protein was significantly more in female pupae of both the hybrids compared to male pupae. There was no difference in protein banding pattern between the sexes and between the hybrids. However, there were differences in amino acids between PM x CSR2 and CSR2 x CSR4 whereas no difference was observed between the two sexes. In the same hybrid, qualitatively protein may be the same but there is difference in their quantities.
The authors are thankful to Dr. S.B. Dandin, Director CSRTI Mysore for providing all the working facility and encouragement.
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